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Clinical Research Scientist Salary in The United States

The average Clinical Research Scientist Salary in The United States is $95,600 per year . Salaries range from $76,600 to $125,600 . The average Clinical Research Scientist Hourly Wage is $54.44 per hour . Hourly wages range from $43.60 to $71.50 . Salaries and wages depend on multiple factors including geographic location, experience, seniority, industry, education etc.

What is the Average Annual Salary of Clinical Research Scientist in The United States ?

What is the Average Hourly Wage of Clinical Research Scientist in The United States ?

Where do Clinical Research Scientists earn more in The United States ?

Other salaries.

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How much does a Clinical Research Associate make in the United States?

• Clinical Research Associate Salary The average Clinical Research Associate salary in the United States is $121,115 as of July 29, 2024. The range for our most popular Clinical Research Associate positions (listed below) typically falls between $58,705 and $183,526. Keep in mind that salary ranges can vary widely depending on many important factors, including position, education, certifications, additional skills, and the number of years you have spent in your profession. With more online, real-time compensation data than any other website, Salary.com helps you determine your exact pay target.

• Clinical Research Associate I Participates in the design, administration and monitoring of clinical trials. Analyzes and evaluates clinical data gathered during research. Ensures compliance with protocol and overall clinical objectives. Knowledge of FDA regulatory requirements is required. May require ACRP or SOCRA Clinical Research Professional exam completion. Requires a bachelor's degree in Science or its equivalent. Typically reports to a supervisor or manager. Work is closely managed. Works on projects/matters of limited complexity in a support role. Typically requires 0-2 years of related experience. View Clinical Research Associate I Salary Alternate Job Titles :Clinical Trials Data Analyst I, Clinical Trials Research Associate I, Clinical Research Associate I Categories : Pharmaceuticals , Biotechnology , Entry Level , Science and Research
• Clinical Research Associate II Participates in the design, administration and monitoring of clinical trials. Analyzes and evaluates clinical data gathered during research. Ensures compliance with protocol and overall clinical objectives. Knowledge of FDA regulatory requirements is required. May require ACRP or SOCRA Clinical Research Professional exam completion. Requires a master's degree in science or equivalent. Typically reports to a supervisor or manager. Occasionally directed in several aspects of the work. Gaining exposure to some of the complex tasks within the job function. Typically requires 2-4 years of related experience. View Clinical Research Associate II Salary Alternate Job Titles :Clinical Trials Data Analyst II, Clinical Trials Research Associate II, Clinical Research Associate II Categories : Pharmaceuticals , Biotechnology , Science and Research
• Clinical Research Manager Manages the clinical monitoring process and the administration of clinical trials. Supervises CRAs in in-house and on-site monitoring, filing, and clinical trial administration. Oversees adherence to SOPs, Good Clinical Practice and FDA regulations. Helps with the development and implementation of clinical processes, procedures, and programs. May require a master's degree in nursing. May require ACRP or SOCRA Clinical Research Professional exam completion. Typically reports to a director. Manages subordinate staff in the day-to-day performance of their jobs. True first level manager. Ensures that project/department milestones/goals are met and adhering to approved budgets. Has full authority for personnel actions. Typically requires 5 years experience in the related area as an individual contributor. 1-3 years supervisory experience may be required. Extensive knowledge of the function and department processes. View Clinical Research Manager Salary Alternate Job Titles :Clinical Research Programs Manager, Clinical Research Manager Categories : Pharmaceuticals , Biotechnology
• Research and Development Associate I Participates in research and development activities. Utilizes established mathematical and scientific techniques to compile and analyze data. Writes technical reports detailing procedures, outcomes, and observations. Requires a bachelor's degree. Typically reports to a supervisor or manager. Works on projects/matters of limited complexity in a support role. Work is closely managed. Typically requires 0-2 years of related experience. View Research and Development Associate I Salary Alternate Job Titles :R & D Support Associate I, Scientific Research Associate I, Research and Development Associate I Categories : Pharmaceuticals , Biotechnology , Energy and Utilities , Science and Research
• Research and Development Associate II Participates in research and development activities. Utilizes established mathematical and scientific techniques to compile and analyze data. Writes technical reports detailing procedures, outcomes, and observations. Requires a bachelor's degree. Typically reports to a supervisor or manager. Gains exposure to some of the complex tasks within the job function. Occasionally directed in several aspects of the work. Typically requires 2 to 4 years of related experience. View Research and Development Associate II Salary Alternate Job Titles :R & D Support Associate II, Scientific Research Associate II, Research and Development Associate II Categories : Pharmaceuticals , Biotechnology , Energy and Utilities , Science and Research
• Research and Development Associate III Participates in research and development activities. Utilizes established mathematical and scientific techniques to compile and analyze data. Writes technical reports detailing procedures, outcomes, and observations. May require a master's degree. Typically reports to a supervisor or manager. Work is generally independent and collaborative in nature. Contributes to moderately complex aspects of a project. Typically requires 4-7 years of related experience. View Research and Development Associate III Salary Alternate Job Titles :R & D Support Associate III, Scientific Research Associate III, Research and Development Associate III Categories : Pharmaceuticals , Biotechnology , Energy and Utilities , Science and Research
• Research and Development Associate IV Participates in research and development activities. Utilizes established mathematical and scientific techniques to compile and analyze data. Writes technical reports detailing procedures, outcomes, and observations. May require a master's degree. Typically reports to a manager or head of a unit/department. Work is highly independent. May assume a team lead role for the work group. A specialist on complex technical and business matters. Typically requires 7+ years of related experience. View Research and Development Associate IV Salary Alternate Job Titles :R & D Support Associate IV, Scientific Research Associate IV, Research and Development Associate IV Categories : Pharmaceuticals , Biotechnology , Energy and Utilities , Science and Research
• Research and Development Associate V Participates in research and development activities. Utilizes established mathematical and scientific techniques to compile and analyze data. Writes technical reports detailing procedures, outcomes, and observations. May require a master's degree. Typically reports to a manager or head of a unit/department. Works autonomously. Goals are generally communicated in "solution" or project goal terms. May provide a leadership role for the work group through knowledge in the area of specialization. Works on advanced, complex technical projects or business issues requiring state of the art technical or industry knowledge. Typically requires 10+ years of related experience. View Research and Development Associate V Salary Alternate Job Titles :R & D Support Associate V, Scientific Research Associate V, Research and Development Associate V Categories : Pharmaceuticals , Biotechnology , Energy and Utilities , Science and Research
• Scientist - Clinical Research Assumes lead role in various clinical research projects. Proposes, plans, organizes and executes experiments and research. Secures grants and funding for research and is responsible for controlling budgets. Summarizes findings in reports and communicates results. Interacts with other scientists within and outside of the organization. Provides recommendations that influence extensive clinical research activities. Requires an advanced degree. Typically reports to head of a unit/department. Work is generally independent and collaborative in nature. Contributes to moderately complex aspects of a project. Typically requires 4 -7 years of related experience. View Scientist - Clinical Research Salary Alternate Job Titles :Clinical Research Lead Scientist, Senior Clinical Researcher, Scientist - Clinical Research Categories : Science and Research , Biotechnology
• Clinical Research Director Directs and oversees the clinical research function for a healthcare organization. Develops research studies and creates standards and guidelines for clinical research services and programs. Ensures adherence to standard operating procedures, good clinical practice and FDA regulations. Requires an advanced degree. Typically reports to top management. Manages a departmental sub-function within a broader departmental function. Creates functional strategies and specific objectives for the sub-function and develops budgets/policies/procedures to support the functional infrastructure. Deep knowledge of the managed sub-function and solid knowledge of the overall departmental function. Typically requires 5+ years of managerial experience. View Clinical Research Director Salary Alternate Job Titles :Clinical Research Programs Director, Clinical Research Director Categories : Healthcare - Administrative , Science and Research

Clinical Researcher salary

Average clinical researcher salary, how much does a clinical researcher make.

The average clinical researcher salary in the United States is $55,453. Clinical researcher salaries typically range between $38,000 and $79,000 yearly. The average hourly rate for clinical researchers is $26.66 per hour.

Clinical researcher salary is impacted by location, education, and experience. Clinical researchers earn the highest average salary in California.

Where can a Clinical Researcher earn more?

Clinical researcher salary estimates from across the web, average clinical researcher salary by state.

The average clinical researcher salary in California, Washington, and Arizona are the highest in the U.S. The lowest average clinical researcher salary states are Alabama, South Carolina, and Kentucky.

• County View

Highest paying states for clinical researchers

Highest paying cities for clinical researchers

The highest-paying cities for clinical researchers are Santa Rosa, CA, Everett, WA, and Worcester, MA.

Clinical Researcher salary details

A clinical researcher's salary ranges from $38,000 a year at the 10th percentile to $79,000 at the 90th percentile.

What is a clinical researcher's salary?

Highest paying clinical researcher jobs

The highest paying types of clinical researchers are clinical project manager, clinical research manager, and senior clinical research associate.

Top companies hiring clinical researchers now:

• Memorial Sloan Kettering Cancer Center Jobs (3)
• Sanofi US Jobs (3)
• Nihon Kohden America Jobs (4)
• Covance Jobs (5)
• Pfizer Jobs (3)

Which companies pay clinical researchers the most?

Clinical researcher salaries at Edwards Lifesciences and Thermo Fisher Scientific are the highest-paying according to our most recent salary estimates. In addition, the average clinical researcher salary at companies like Novo Nordisk and University of Maryland, Baltimore are highly competitive.

Wage gap by gender, race and education

Clinical researcher salary by industry.

The average clinical researcher salary varies across industries:

• The average clinical researcher salary in the pharmaceutical industry is $58,800, the highest of any industry.
• The average clinical researcher salary in the finance industry is $53,851.
• Clinical researchers in the education industry earn an average salary of $48,344, the lowest of any industry.

Highest paying industries for clinical researchers

High Paying Clinical Researcher Jobs

Clinical researcher salary trends.

The average clinical researcher salary has risen by $9,315 over the last ten years. In 2014, the average clinical researcher earned $46,138 annually, but today, they earn $55,453 a year. That works out to a 15% change in pay for clinical researchers over the last decade.

Compare clinical researcher salaries for cities or states with the national average over time.

Average clinical researcher salary over time

Compare clinical researcher salaries for individual cities or states with the national average.

Clinical Researcher salary by year

Recently added clinical researcher salaries

Clinical Researcher salary FAQs

What state pays clinical researchers the most, how do i know if i'm being paid fairly as a clinical researcher.

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Clinical Researcher Related Salaries

• Clinical Associate Salary
• Clinical Coordinator Salary
• Clinical Project Manager Salary
• Clinical Research Assistant Salary
• Clinical Research Associate Salary
• Clinical Research Coordinator Salary
• Clinical Research Manager Salary
• Clinical Trial Coordinator Salary
• Clinical Trial Manager Salary
• Coordinator And Research Assistant Salary
• Research Administrator Salary
• Research Coordinator Salary
• Research Nurse Salary
• Research Project Coordinator Salary
• Researcher Salary

Clinical Researcher Related Careers

• Clinical Associate
• Clinical Coordinator
• Clinical Project Manager
• Clinical Research Assistant
• Clinical Research Associate
• Clinical Research Coordinator
• Clinical Research Manager
• Clinical Trial Coordinator
• Clinical Trial Manager
• Coordinator And Research Assistant
• Research Administrator
• Research Coordinator
• Research Nurse
• Research Project Coordinator

Clinical Researcher Related Jobs

• Senior Clinical Research Associate
• Senior Program Coordinator
• Senior Research Associate

What Similar Roles Do

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• What Does a Clinical Trial Coordinator Do
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Average Clinical Research Associate (CRA) Salary

The average salary for a Clinical Research Associate (CRA) is $74,947 in 2024

Featured Content

What is the pay by experience level for clinical research associate (cra)s .

An entry-level Clinical Research Associate (CRA) with less than 1 year experience can expect to earn an average total compensation (includes tips, bonus, and overtime pay) of $62,775 based on 240 salaries. An early career Clinical Research Associate (CRA) with 1-4 years of experience earns an average total compensation of …Read more

What Do Clinical Research Associate (CRA)s Do?

Clinical research associates (CRA) are responsible for assisting in the clinical research process, providing advanced technical expertise in steps such as handling supplies, ordering tests, and collecting results, presenting specific research information to the public, and a variety of administrative tasks. CRAs must follow strict privacy and safety regulations to prevent problems with subjects and ethical concerns; they must also be organized and pay close attention to detail when conducting …Read more

How do Clinical Research Associate (CRA)s Rate Their Jobs?

Common health benefits for a clinical research associate (cra), gender breakdown for clinical research associate (cra)s.

FAQs About Clinical Research Associate (CRA)s

What is the highest pay for clinical research associate (cra)s.

Our data indicates that the highest pay for a Clinical Research Associate (CRA) is $105k / year

What is the lowest pay for Clinical Research Associate (CRA)s?

Our data indicates that the lowest pay for a Clinical Research Associate (CRA) is $50k / year

How can Clinical Research Associate (CRA)s increase their salary?

Increasing your pay as a Clinical Research Associate (CRA) is possible in different ways. Change of employer: Consider a career move to a new employer that is willing to pay higher for your skills. Level of Education: Gaining advanced degrees may allow this role to increase their income potential and qualify for promotions. Managing Experience: If you are a Clinical Research Associate (CRA) that oversees more junior Clinical Research Associate (CRA)s, this experience can increase the likelihood to earn more.

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• United States

Clinical Research Associate

$87,326 (usd)/yr, $41.98 (usd) /hr, $1,947 (usd) /yr.

The average clinical research associate gross salary in United States is $87,326 or an equivalent hourly rate of $42. In addition, they earn an average bonus of $1,947. Salary estimates based on salary survey data collected directly from employers and anonymous employees in United States. An entry level clinical research associate (1-3 years of experience) earns an average salary of $62,542. On the other end, a senior level clinical research associate (8+ years of experience) earns an average salary of $107,761.

Data powered by ERI's Salary Expert Database .

This page is a promotion for SalaryExpert’s Assessor Platform and is not intended for professional use.

Professionals should subscribe to SalaryExpert’s Assessor Platform .

ERI’s compensation data are based on salary surveys conducted and researched by ERI. Cost of labor data in the Assessor Series are based on actual housing sales data from commercially available sources, plus rental rates, gasoline prices, consumables, medical care premium costs, property taxes, effective income tax rates, etc.

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$98,090 (USD)

Based on our compensation data, the estimated salary potential for Clinical Research Associate will increase 12 % over 5 years.

This chart displays the highest level of education for: Clinical Research Associate , the majority at 100% with bachelors.

Typical Field of Study: Community Organization and Advocacy

the United States

Cost of living is calculated based on accumulating the cost of food, transportation, health services, rent, utilities, taxes, and miscellaneous.

The United States of America (USA or U.S.A.), commonly known as the United States (US or U.S.) or America, is a country primarily located in North America. It is a federal union of 50 states, which also includes its federal capital district of Washington, D.C., and 326 Indian reservations. The 48 contiguous states are bordered by Canada to the north and Mexico to the south. The State of Alaska is non-contiguous and lies to the northwest, while the State of Hawaii is an archipelago in the Pacific...

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Clinical Research Coordinator Associate

🔍 school of medicine, stanford, california, united states.

The Clinical Research Coordinator Associate is responsible for the overall management and implementation of an assigned set of multiple research protocols assuring efficiency and regulatory compliance. These studies will be conducted at the Stanford Hospital and Clinics. He/she will work as part of a clinical trials research team and report to various Principal Investigators conducting clinical research. Responsibilities include preparation of initial study documents for IRB submission in compliance with all local, state and federal regulations; advise the IRB of amendment changes to the protocol and complete annual protocol renewals. Recruit, screen, assist in the informed consent process and enroll subjects in accordance with good clinical practice guidelines. Collect, record and maintain complete data files using good clinical practice in accordance to HIPAA regulations. He/she participates in data retrieval, reporting, and preparation of files and Case Report Forms for the various studies. The successful candidate will interact with subjects by scheduling diagnostic and research evaluation visits, perform study related assessments including collection of blood samples, processing and shipment. Maintain drug accountability, adequate study supplies and equipment. The coordinator will oversee subject compliance to the study protocol, obtain information from the study subject regarding any changes in their medications or adverse events and promptly report the findings to physicians for documentation in the subject’s medical record. Report all serious adverse events promptly to investigators, sponsors and the IRB. Protect the rights, safety and well-being of human subjects involved in the clinical trials. 

Duties include*:

• Serve as primary contact with research participants, sponsors, and regulatory agencies.  Coordinate studies from startup through close-out.
• Determine eligibility of and gather consent from study participants according to protocol.  Assist in developing recruitment strategies.
• Coordinate collection of study specimens and processing.
• Collect and manage patient and laboratory data for clinical research projects.  Manage research project databases, develop flow sheets and other study related documents, and complete study documents/case report forms. 
• Ensure compliance with research protocols, and review and audit case report forms for completion and accuracy with source documents.  Prepare regulatory submissions, and ensure institutional Review Board renewals are completed.
• Assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents, and attend monitoring meetings with sponsors, acting as primary contact.
• Monitor expenditures and adherence to study budgets and resolve billing issues in collaboration with finance and/or management staff.
• Interact with the principal investigator regularly, ensuring patient safety and adherence to proper study conduct. 
• Ensure essential documentation and recording of patient and research data in appropriate files per institutional and regulatory requirements.
• Participate in monitor visits and regulatory audits. 

* - Other duties may also be assigned

EDUCATION & EXPERIENCE (REQUIRED):

Two year college degree and two years related work experience or a Bachelor’s degree in a related field or an equivalent combination of related education and relevant experience. 

KNOWLEDGE, SKILLS AND ABILITIES (REQUIRED):

• Strong interpersonal skills.
• Proficiency with Microsoft Office.
• Knowledge of medical terminology.

CERTIFICATIONS & LICENSES:

Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred. 

PHYSICAL REQUIREMENTS*:

• Frequently stand, walk, twist, bend, stoop, squat and use fine light/fine grasping. 
• Occasionally sit, reach above shoulders, perform desk based computer tasks, use a telephone and write by hand, lift, carry, push, and pull objects that weigh up to 40 pounds.
• Rarely kneel, crawl, climb ladders, grasp forcefully, sort and file paperwork or parts, rarely lift, carry, push, and pull objects that weigh 40 pounds or more.

* - Consistent with its obligations under the law, the University will provide reasonable accommodation to any employee with a disability who requires accommodation to perform the essential functions of his or her job. WORKING CONDITIONS: 

Occasional evening and weekend hours.

WORK STANDARDS:

• Interpersonal Skills: Demonstrates the ability to work well with Stanford colleagues and clients and with external organizations.
• Promote Culture of Safety: Demonstrates commitment to personal responsibility and value for safety; communicates safety concerns; uses and promotes safe behaviors based on training and lessons learned.
• Subject to and expected to comply with all applicable University policies and procedures, including but not limited to the personnel policies and other policies found in the University's Administrative Guide, http://adminguide.stanford.edu .

The expected pay range for this position is $31.73 to $36.54 per hour.

Stanford University provides pay ranges representing its good faith estimate of what the university reasonably expects to pay for a position. The pay offered to a selected candidate will be determined based on factors such as (but not limited to) the scope and responsibilities of the position, the qualifications of the selected candidate, departmental budget availability, internal equity, geographic location and external market pay for comparable jobs.

At Stanford University, base pay represents only one aspect of the comprehensive rewards package. The Cardinal at Work website ( https:/lcardinalatwork.stanford.edu/benefits-rewards ) provides detailed information on Stanford's extensive range of benefits and rewards offered to employees. Specifics about the rewards package for this position may be discussed during the hiring process.

Consistent with its obligations under the law, the University will provide reasonable accommodations to applicants and employees with disabilities. Applicants requiring a reasonable accommodation for any part of the application or hiring process should contact Stanford University Human Resources at [email protected]. For all other inquiries, please submit a contact form .

Stanford is an equal employment opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.

The job duties listed are typical examples of work performed by positions in this job classification and are not designed to contain or be interpreted as a comprehensive inventory of all duties, tasks, and responsibilities. Specific duties and responsibilities may vary depending on department or program needs without changing the general nature and scope of the job or level of responsibility. Employees may also perform other duties as assigned.

• Schedule: Full-time
• Job Code: 1013
• Employee Status: Regular
• Requisition ID: 104161
• Work Arrangement : Hybrid Eligible

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COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK

Clinical Research Coordinator

• Obstetrics and Gynecology
• Columbia University Medical Center
• Opening on: Aug 13 2024
• Job Type: Officer of Administration
• Bargaining Unit:
• Regular/Temporary: Regular
• End Date if Temporary:
• Hours Per Week: 35
• Standard Work Schedule:
• Salary Range: $64,000 - $66,000

Position Summary

The primary role of this position is to support clinical research involving Maternal Fetal Medicine Research. The employee will interact with pregnant women, their families and clinical staff as it relates to clinical research protocols and clinical trials, industry funded and grant funded, being implemented in the inpatient and outpatient setting. The inpatient setting includes labor and delivery, ante-partum and post-partum.  The outpatient setting includes ACN clinics, Columbia doctor’s private offices, and ultrasound units.

Responsibilities

• Complete of GCP, HIPAA and applicable regulatory training.
• Complete certification requirements for assigned protocols.
• Screen designated schedules or patient lists for eligible subjects.
• Contact, approach and verify eligibility subjects.
• Screen, enroll and consent eligible subjects.
• Complete research study visits as delineated in assigned protocol and manual of operations set forth by sponsor and supervisor.
• Complete Telephone follow-up and telephone reminder calls for study participants, during these phone calls the person will need to administer study questionnaire as assigned.
• Coordinate the collection of all research data points as assigned, whether through research visits, chart abstraction or telephone.
• Schedule of research visits.
• Enter research data into a centralized database program and other study specific electronic databases.
• Collect through venipuncture, process, track, transport and ship biological specimens (including birth specimens) as assigned and by steps delineated in the protocol or manual of operations.
• Complete study documents and files some examples might include case report forms, worksheets and medical record notes.
• Maintain confidentiality of documents and files such as HIPAA.
• Inform relevant clinical staff regarding subject protocol participation.
• Assist in other research related activities and projects as needed.
• Collaborate regularly with the investigators and other research staff.
• Consult with medical records of outlying clinics and hospitals to obtain pertinent data and patient information.
• Interface with various hospital departments such as medical records, radiology, nursing, information technology services, and others as needed.
• Attend and participate in Investigator, site initiation and monitoring meetings as assigned.
• Participate in on-call activities to cover research activity off- hours as needed.
• Perform other related duties and responsibilities as assigned/requested.

Minimum Qualifications

• Requires a bachelor's degree or equivalent in education and experience.
• Phlebotomy Certified (or other forms of certification in lieu of phlebotomy such as certified medical assistant, nurse degree (LPN, RN) - current or obtained within 3 months.
• Complete proficiency in written and spoken English and Spanish.
• Incumbent must be self-directed and able to make independent decision within the parameters of all federal, state, institutional and departmental guidelines.

Preferred Qualifications

• Experience in a patient care setting and clinical research experience.
• Excellent interpersonal, written/oral communication, and organizational skills.
• Proficiency in Microsoft Office.
• Master’s or another advanced degree may substitute in part for experience.

The Department of Obstetrics and Gynecology is dedicated to the goal of building a multicultural faculty and staff committed to teaching, working and serving in a diverse community, and strongly encourages applications from candidates of traditionally underrepresented backgrounds.

We are continuously seeking to recruit individuals who will enhance the diversity of our workplace and the effectiveness of our organization.

Equal Opportunity Employer / Disability / Veteran

Columbia University is committed to the hiring of qualified local residents.

Commitment to Diversity 

Columbia university is dedicated to increasing diversity in its workforce, its student body, and its educational programs. achieving continued academic excellence and creating a vibrant university community require nothing less. in fulfilling its mission to advance diversity at the university, columbia seeks to hire, retain, and promote exceptionally talented individuals from diverse backgrounds.  , share this job.

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Get an NIH Salary Award So You Can Develop Research Software

If you’re currently in a non-tenure track position at an academic or research institution, you can apply for funding to develop your career as a Research Software Engineer (RSE). As the grant recipient, you’ll serve as the principal investigator (PI) for up to three years. You’ll have the opportunity to expand your knowledge in the development and dissemination of biomedical, clinical, behavioral, or health-related research software, tools, and algorithms.

To be an ideal candidate, you must:

• have held a full-time, non-tenure track position for at least one year.
• demonstrate outstanding software engineering research expertise with relevant publications, peer-reviewed conference proceedings, and links to code samples.
• commit to a minimum effort of six “person-months” (i.e., number of people multiplied by the number of months they work).
• not have served as the contact PI for any independent NIH grant applications in the past five years.

NIH aims to update the data ecosystem by building sustainable software foundations for open software and tools in biomedical, clinical, behavioral, and health-related research. This effort aligns with the NIH Strategic Plan for Data Science and encourages the adoption of solid software development practices, new data science technologies, cloud and hybrid computing, artificial intelligence, and open science guidelines.

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Regulatory Coordinator

• Madison, Wisconsin
• SCHOOL OF MEDICINE AND PUBLIC HEALTH/FAMILY MEDICINE-GEN
• Compliance, Legal, and Protection
• Partially Remote
• Staff-Full Time
• Staff-Part Time
• Opening at: Aug 13 2024 at 16:00 CDT
• Closing at: Aug 27 2024 at 23:55 CDT

Job Summary:

The Regulatory Coordinator provides comprehensive investigator support services for clinical research in the Department of Family Medicine and Community Health at the UW School of Medicine and Public Health (SMPH). To carry out these activities, the incumbent will work closely with both the Health Sciences Institutional Review Board (HS-IRB) and the Health Sciences Minimal Risk Institutional Review Board (MR-IRB). This position reports to the Director of Research Operations. This position is responsible for distilling complex scientific protocols into clear, concise, and accurate clinical research applications, consent forms, and correspondence. Most critical is the ability to manage many detailed projects simultaneously, completing projects in a timely manner, and meeting strict deadlines required by review committees, boards, as well as, by investigators and sponsors of clinical research.

Responsibilities:

• 15% Develops, prepares, and submits protocol-specific application materials to regulatory bodies such as the Institutional Review Board and scientific review committee
• 15% Develops clear and accurate informed consent documents
• 20% Serves as regulatory contact person for research studies involving human subjects
• 15% Maintains complete and accurate regulatory files and records
• 5% Communicates directly with protocol sponsors related to regulatory documents and activities
• 15% Provides guidance and direction to research teams regarding compliance with policies, procedures, and regulations
• 5% Performs quality checks
• 5% May lead and train other staff
• 5% Contributes to the development of new team and unit processes, procedures, tools, and training

Institutional Statement on Diversity:

Diversity is a source of strength, creativity, and innovation for UW-Madison. We value the contributions of each person and respect the profound ways their identity, culture, background, experience, status, abilities, and opinion enrich the university community. We commit ourselves to the pursuit of excellence in teaching, research, outreach, and diversity as inextricably linked goals. The University of Wisconsin-Madison fulfills its public mission by creating a welcoming and inclusive community for people from every background - people who as students, faculty, and staff serve Wisconsin and the world. For more information on diversity and inclusion on campus, please visit: Diversity and Inclusion

Preferred Bachelor's Degree

Qualifications:

Required Qualifications: - Experience with Institutional Review Board (IRB) submissions or equivalent-types of submissions. - Experience communicating effectively (written and oral) with faculty investigators, research coordinators, sponsors, and staff at all levels. - Independent problem-solving and analytical skills. - Ability to manage multiple projects simultaneously. - Demonstrated attention to detail and time management skills, including experience with accurate and timely documentation. Preferred Qualifications: - Experience with relevant computer software systems and web based programs, including minimum proficiency in Microsoft Office Suite and experience with Application Review for Research Oversight at Wisconsin (ARROW). - Experience working with human subjects research, grants, scientific writing, health care, and/or working in an academic setting. - Knowledge of federal human subjects protection regulations. - Prior experience obtaining Center for Medicare and Medicaid Services (CMS) approval for research studies. - In-depth understanding of and/or willing and able to learn about University of Wisconsin administrative policies and procedures as well as applicable state and federal regulations and guidelines.

Full or Part Time: 75% - 100% This position may require some work to be performed in-person, onsite, at a designated campus work location. Some work may be performed remotely, at an offsite, non-campus work location.

Appointment Type, Duration:

Ongoing/Renewable

Minimum $63,126 ANNUAL (12 months) Depending on Qualifications The starting salary for the position is $63,126 but is negotiable based on experience and qualifications. Employees in this position can expect to receive benefits such as generous vacation, holidays, and sick leave; competitive insurances and savings accounts; retirement benefits. Benefits information can be found at: https://hr.wisc.edu/benefits/ SMPH Academic Staff Benefits flyer: https://uwmadison.box.com/s/r50myohfvfd15bqltljn0g4laubuz7t0

Additional Information:

The University of Wisconsin Department of Family Medicine and Community Health is a large, tier-one clinical department in the UW School of Medicine and Public Health (SMPH). UW DFMCH has 171 faculty, 261 adjunct faculty, and 110 staff located throughout the state. Combined with its associated UW Health clinic operation, the department boasts over 750 total employees transforming health care in Wisconsin. The DFMCH is committed to patient care while also offering outstanding educational and research programs. There are over 150 residents in our sponsored and academic partner programs, and more than 400 medical students train in the department each year, with the Madison residency program ranking fifth in the nation for 2023. In fiscal year 2022, our physicians and residents practicing at 17 clinics throughout the state managed over 358,000 patient visits - an integral part of the department's success. Learn more about our department's work by visiting https://www.fammed.wisc.edu/ and DFMCH Diversity, Equity and Inclusion: https://www.fammed.wisc.edu/diversity/ University sponsorship is not available for this position, including transfers of sponsorship. The selected applicant will be responsible for ensuring their continuous eligibility to work in the United States (i.e. a citizen or national of the United States, a lawful permanent resident, a foreign national authorized to work in the United States without the need of an employer sponsorship) on or before the effective date of appointment. This position is an ongoing position that will require continuous work eligibility. UW-Madison is not an E-Verify employer, and therefore, is not eligible to employ F1 STEM OPT Extension participants. If you are selected for this position you must provide proof of work authorization and eligibility to work.

How to Apply:

To apply for this position, please click on the "Apply Now" button. You will be asked to upload a current resume/CV and a cover letter briefly describing your qualifications and experience.

Paige Steinert [email protected] 608-890-1740 Relay Access (WTRS): 7-1-1. See RELAY_SERVICE for further information.

Official Title:

Regulatory Coordinator(CP085)

Department(s):

A53-MEDICAL SCHOOL/FAMILY MED/RES GENERAL

Employment Class:

Academic Staff-Renewable

Job Number:

The university of wisconsin-madison is an equal opportunity and affirmative action employer..

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