1,000+ matching jobs for “Clinical Research Associate”

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Thermo Fisher Scientific

FSP Clinical Trial Coordinator Finland

Remote, Finland

Join Us as a Clinical Trial Coordinator II – Make an Impact at the Forefront of Innovation We have successfully supported the top …

Added Oct 16, 2026

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Labcorp Holdings

Research Study Technician-Pathology (Early Talent)

Greenfield, Indiana, United States

Full time
Regular

… Qualifications: Bachelor’s degree in Animal Science, Biology, Chemistry, Microbiology, Biochemistry OR Associate’s degree in Veterinary Technology/ Veterinary Nursing Preferred Qualifications 6 months or more of …

Added Oct 16, 2026

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Stryker

Summer 2027 Internship - Clinical Affairs - Michigan

Portage, Michigan, United States

… to ensure a thorough understanding of available treatment options and clinical studies Accompany Clinical Research Associate to monitor clinical data at clinical investigative sites Prepare literature review summaries for …

Added Oct 27, 2026

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IQVIA Holdings

MedTech Clinical Educator RN

Fort Worth, Texas, United States +3 locations

… education needs and collaborate with staff to deliver a positive educational experience Utilize clinical nursing expertise to answer questions and address concerns with the medical device Provide updates, …

Added Oct 15, 2026

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IQVIA Holdings

Clinical Trials Regulatory Officer - Regulatory Maintenance

Zagreb, Croatia +7 locations

focuses on preparing and maintaining global core clinical trial submission dossiers, supporting EU Clinical Trials Regulation (CTR) modifications, and providing …

Added Oct 15, 2026

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Abbott Laboratories

Manager Clinical Site Operations, Site ICRA

Maple Grove, Minnesota, United States +1 location

Pay posted by employer$99,300–$198,700

… TX or Sylmar, CA locations. This position is responsible for the supervision of a team of personnel within Clinical Site Operations (CSO) which supports US, Canada, and LATAM. Assists management in hiring, training, …

Added Oct 23, 2026

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Labcorp Holdings

Clinical Laboratory Supervisor – Patient Services

Manhattan KS +1 location

Full time
Regular

… schedule adequate assay coverage Responsible for ensuring all shifts in the department are properly staffed Research and resolve any production errors while escalating when necessary Engage in continuous process and service …

Added Oct 16, 2026

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Abbott Laboratories

Clinical Site Lead – Atlanta, GA Territory

Atlanta, Georgia, United States

Pay posted by employer$61,300–$122,700

… for diversity, working mothers, female executives, and scientists. The Opportunity We are recruiting for a Clinical Site Lead to join our field team for the Atlanta, GA and surrounding territory. The Clinical Site Lead …

Added Oct 21, 2026

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Merck (MSD)

Senior Director, Clinical Development Metabolism (MASH)

Rahway, New Jersey, United States +2 locations

Pay posted by employer$282,200–$444,200

Added Oct 16, 2026

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Abbott Laboratories

Sr. Clinical Site Lead- Philadelphia, PA

United States - Illinois - Abbott Park

Pay posted by employer$78,000–$156,000

… best place to work for diversity, working mothers, female executives, and scientists. The Opportunity The Clinical Site Lead drives study execution and operational excellence across Abbott Cardiovascular therapies …

Added Oct 15, 2026

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Labcorp Holdings

Research Study Technician - Animal Operations (Early Talent)

Madison WI

Full time
Regular

As a Research Study Technician, you’ll apply your scientific curiosity in researching the effectiveness, safety and …

Added Oct 16, 2026

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IQVIA Holdings

Clinical Files Specialist (CTA BackUp - Entrylevel position)

Buenos Aires, Argentina

Clinical Files Specialist - Entry Level role Work modality: Hybrid Job Overview Perform daily administrative …

Added Oct 15, 2026

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IQVIA Holdings

Clinical Trial Assistant 1- Sponsor dedicated- Netanya

Netanya, Israel

Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File …

Added Oct 15, 2026

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Abbott Laboratories

Sr. Clinical Affairs Specimen Operations Specialist

Madison, Wisconsin, United States +1 location

Pay posted by employer$78,000–$156,000

Position Overview The Sr. Clinical Affairs Specimen Operations Specialist leads planning and execution of specimen logistics for clinical …

Added Oct 15, 2026

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Stryker

Summer 2027 Internship - Clinical Affairs - New Jersey

Mahwah, New Jersey, United States

Added Oct 27, 2026

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Thermo Fisher Scientific

FSP_Clinical Trial Coordinator (Sponsor: Roche)

Remote, Korea, Republic of

… team, you’ll have the opportunity to provide administrative and technical support to the Project Team. As a Clinical Operations Delivery Associate II, you'll support audit readiness by ensuring files are reviewed according …

Added Oct 25, 2026

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Abbott Laboratories

Sr. Clinical Laboratory Scientist - Weekend PM

United States > Madison : 650 Forward Dr

Pay posted by employer$26.50–$53.00 per hour

Position Overview The Senior Clinical Laboratory Scientist will be responsible for performing moderate and high complexity laboratory testing on …

Added Oct 15, 2026

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IQVIA Holdings

Clinical Trial Assistant, HYBRID in Wilmington, DE

Wilmington, Delaware, United States

Pay posted by employer$35,800–$123,000

Essential Functions • Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining …

Added Oct 15, 2026

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Johnson & Johnson

Associate Clinical Consultant (San Francisco East Bay Area) - Johnson & Johnson MedTech, Heart Recovery

Walnut Creek, California, United States +1 location

Full time
Regular

Pay posted by employer$122,000–$137,000

… Ramon Walnut Creek Concord Pleasant Hill Oakland Danville Dublin We are searching for the best talent for Associate Clinical Consultant. About Cardiovascular Fueled by innovation at the intersection of biology and …

Added Oct 15, 2026

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Abbott Laboratories

Sr. Clinical Laboratory Scientist - 3rd Shift

Madison, Wisconsin, United States +1 location 2 postings

Pay posted by employer$26.50–$53.00 per hour

Position Overview The Senior Clinical Laboratory Scientist will be responsible for performing moderate and high complexity laboratory testing on …

Added Oct 15, 2026

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Merck (MSD)

Senior Director, Clinical Development Metabolism (MASH)

Rahway, New Jersey, United States +2 more

Pay posted by employer$282,200–$444,200

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Qualifications · employer excerpt

Education
M.D or M.D./Ph.D.
Required
Must have experience in industry or as senior faculty in academia
Minimum of 3 years of experience in clinical medicine

6 more in the full description below.

About this opportunity

Original employer description

Job Description

The Senior Director (Sr. Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed medicines in the Metabolism section of the Atherosclerosis & Metabolism therapeutic area, with a particular focus on MASH (Metabolic Dysfunction-Associated Steatohepatitis) and other obesity-related disorders. Our company's Atherosclerosis & Metabolism medicines span all phases of clinical development (pre-clinical to post-licensure). The Senior Director will manage the entire cycle of late-stage clinical development and studies, including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication.

Specifically, the Senior Director May Be Responsible For:

Planning clinical trials (design, operational plans, settings) based on these clinical development strategies
Monitoring and managing the conduct of ongoing or new clinical trials for investigational or marketed drugs
Analyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication
Participation in internal and joint internal/external research project teams relevant to the development of new compounds, and the further study of marketed compounds.
Evaluating pre-clinical and translational work for the purpose of generating early clinical development plans and Investigational New Drug applications;
Developing clinical development strategies for investigational or marketed drugs
Support of business development assessments of external opportunities

The Senior Director May:

Work closely with the Clinical Scientists in the execution of clinical studies. Work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects; and assist the Executive Director and/or Associate Vice President in ensuring that appropriate Corporate personnel are informed of the progress of studies of our company and competitors' drugs, and of internal and external expert opinion on scientific questions relevant to his/her areas of responsibility.

The Senior Director is responsible for maintaining a strong scientific fund of knowledge by:

Maintaining awareness of scientific developments within his/her area of expertise, in terms of new scientific findings and research methodologies
Identifying scientifically and operationally strong investigators who can assist in the development of our company's investigational and marketed drugs
Establishing communications with prominent clinical investigators in his/her particular field of interest, particularly those who will be willing and able to assist in the evaluation of our company's drugs
Attending appropriate scientific meetings to maintain his or her competency and to maintain awareness of research activities in his/her area of responsibility.

To accomplish these goals, the Senior Director may:

Author detailed development documents, presentations, budgets, and position papers for internal and external audiences.
Facilitate collaborations with external researchers around the world.
Travel on company business about twenty (20) percent of the time to manage future or ongoing clinical research projects.

Qualifications

Education

M.D or M.D./Ph.D.

Required

Must have experience in industry or as senior faculty in academia
Minimum of 3 years of experience in clinical medicine
Minimum of 3-5 years of industry experience in drug development or biomedical research experience in academia
Demonstrated success in overseeing clinical studies and protocols
Demonstrated record of scientific scholarship and achievement
Proven track record in clinical medicine and background in biomedical research
Strong interpersonal skills, as well as the ability to function in a team environment
Outstanding verbal and written communication and presentation skills

Preferred

Board Certified or Eligible in Endocrinology, Gastroenterology, Hepatology or related discipline

Direct clinical research experience in MASH, with a preference for candidates who have designed, executed, or medically monitored Phase 2 or Phase 3 trials in metabolic liver diseases

Required Skills:

Cardiology, Clinical Development, Clinical Trials, Drug Development, Endocrinology, Hepatology, Liver Diseases, Nephrology, Obesity, Pharmaceutical Industry

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

US and Puerto Rico Residents Only:

Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.

As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:

EEOC Know Your Rights

EEOC GINA Supplement

We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively.

Learn more about your rights, including under California, Colorado and other US State Acts

The primary location for this posting is:

USA - New Jersey - Rahway

Where required by law, the compensation range for this role is provided below.

The salary range for the primary location of this role is:

$282,200.00 - $444,200.00

This range reflects the Company's reasonable expectation of the base salary applicable to this role at the time of posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs. The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.

We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.

Additional location(s): Please note the salary range above applies to the Primary Location of the position. Where a role has other listed locations, different compensation guidelines may apply. You may find the salary ranges for additional locations below. If the salary range is not listed for the location you are applying to, our Talent Acquisition team will provide further information to you relevant to your location.

Additional location(s) Compensation Information:

San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance

Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance

Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status:

Regular

Relocation:

Domestic

VISA Sponsorship:

Yes

Travel Requirements:

25%

Flexible Work Arrangements:

Not Applicable

Shift:

Not Indicated

Valid Driving License:

Hazardous Material(s):

n/a

Job Posting End Date:

10/29/2026

*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

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