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

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Thermo Fisher Scientific

FSP Clinical Research Associate I/Clinical Research Associate II - Central Poland

Remote, Poland

Join Us as a Clinical Research Associate I – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical …

Added Oct 16, 2026

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IQVIA Holdings

Clinical Research Associate - Sponsor Dedicated

Parsippany, New Jersey, United States +4 locations

Pay posted by employer$74,500–$197,500

… monitoring experience within the pharmaceutical, biotechnology, or CRO industry. Strong understanding of clinical research processes and regulatory requirements, including GCP and ICH guidelines. Knowledge of therapeutic …

Added Oct 15, 2026

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Merck (MSD)

Associate Director, Clinical Research Associate Manager

IND - Maharashtra - Mumbai (WeWork)

Associate Director, Clinical Research Associate Manager This role will be key to ensure strong monitoring in our clinical trials. Under the oversight of …

Added Oct 16, 2026

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IQVIA Holdings

Senior Clinical Research Associate, Early Clinical Development

Carlsbad, California, United States +2 locations

Pay posted by employer$90,200–$175,100

… initiation, monitoring, and close-out in alignment with the contracted scope of work, Good Clinical Practice (GCP), and ICH guidelines. Collaborate with site staff to implement and track subject recruitment …

Added Oct 15, 2026

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Thermo Fisher Scientific

(Sr) Clinical Research Associate - Belgium

Remote, Belgium

Join Us as a Senior Clinical Research Associate – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical …

Added Oct 16, 2026

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IQVIA Holdings

(Senior) Clinical Research Associate, IQVIA

Durham, North Carolina, United States

Pay posted by employer$90,200–$175,100

… to manage multiple priorities in a fast-paced environment Why Join Us Make a direct impact on advancing clinical research and improving patient outcomes Work alongside experienced, collaborative teams Opportunities for …

Added Oct 15, 2026

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Thermo Fisher Scientific

FSP Clinical Research Associate II

Remote, Vietnam

Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 …

Added Oct 16, 2026

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Thermo Fisher Scientific

FSP Clinical Research Associate I

Vietnam, Vietnam

Job Description Join Us as a Clinical Research Associate – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical …

Added Oct 16, 2026

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Merck (MSD)

Clinical Research Associate Manager (Remote)

USA - New Jersey - Rahway +1 location

Pay posted by employer$142,400–$224,100

This role will be key to ensure strong monitoring in our clinical trials. Under the oversight of the Clinical Research Director (CRD) or Head of Site Management and …

Added Oct 16, 2026

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IQVIA Holdings

Clinical Research Associate (Client Dedicated)

Bangkok, Thailand

… and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Work with sites to adapt, …

Added Oct 15, 2026

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Thermo Fisher Scientific

FSP Clinical Research Associate II

Taguig City, Philippines +2 locations 4 postings

Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 …

Added Oct 16, 2026

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Thermo Fisher Scientific

FSP Clinical Research Associate II

Remote, Mexico +1 location 2 postings

Job Description Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 …

Added Oct 16, 2026

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IQVIA Holdings

Senior Clinical Research Associate, Early Clinical Development

Durham, North Carolina, United States

Pay posted by employer$87,200–$169,300

Added Oct 15, 2026

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Thermo Fisher Scientific

FSP Clinical Research Associate II

Remote, Romania

Join Us as a FSP Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 …

Added Oct 16, 2026

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Thermo Fisher Scientific

Sr Clinical Research Associate - FSP

Remote, Hungary

Join Us as a Senior Clinical Research Associate (Level I) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 …

Added Oct 16, 2026

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Thermo Fisher Scientific

Clinical Research Associate II (FSP)

Melbourne, Australia +1 location

… environment, making sure our food is safe or helping find cures for cancer. About the Role: Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 …

Added Oct 16, 2026

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IQVIA Holdings

Clinical Research Associate 2 - CFSP

Madrid, Spain +1 location

… the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines Managing progress by tracking regulatory …

Added Oct 15, 2026

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IQVIA Holdings

Clinical Research Associate, Sponsor Dedicated

Durham, North Carolina, United States +84 locations

Pay posted by employer$74,500–$197,500

… care preferred. • Requires at least 2 years of year of independent on-site monitoring experience as a Clinical Research Associate (CRA) in a CRO, sponsor, or similar setting. • Equivalent combination of education, training and experience …

Added Oct 15, 2026

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IQVIA Holdings

Clinical Research Associate , Multisponsor Team

Bucharest, Romania

Join us in our exciting journey!! IQVIA is looking for a Clinical Research Associate to provide service to the multisponsor team. You would be responsible for: Performing visits (such as …

Added Oct 15, 2026

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IQVIA Holdings

Clinical Research Associate, Sponsor Dedicated

Carlsbad, California, United States +1 location

Pay posted by employer$71,900–$189,000

… Qualifications • Requires a minimum of 1 year of independent on-site monitoring experience as a Clinical Research Associate (CRA). • Bachelor's Degree in scientific discipline or health care preferred. • Equivalent combination of …

Added Oct 15, 2026

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Merck (MSD)

Clinical Research Associate Manager (Remote)

USA - New Jersey - Rahway +1 more

Pay posted by employer$142,400–$224,100

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Required Skills · employer excerpt

Current Employees apply HERE
Current Contingent Workers apply HERE

About this opportunity

Original employer description

Job Description

This role will be key to ensure strong monitoring in our clinical trials. Under the oversight of the Clinical Research Director (CRD) or Head of Site Management and Monitoring, the person is responsible to manage a team of 6-14 Clinical Research Associates (CRAs)and to ensure excellent study and site performance with strict adherence to local regulations, company SOPs and ICH GCP.

As Associate Director, the role is critical to continuously develop key talents by providing training, support and mentoring to the CRAs and properly manage situation of low or non-performance.

The role will work at country level with other local stakeholder e.g. Clinical Research Managers (CRM) to ensure alignment and development of the country capabilities. The role will collaborate with country Partner Line Managers (PLMs) to ensure alignment across all monitoring functions. The person contributes to HQ capacity/resource planning activities to ensure efficient allocation of resources and work.

This person will work primarily in Vaccine/Infectious Disease with some Cardiovascular therapeutic areas.

Responsibilities:

Work allocation, staff development and performance appraisal.
Support departmental company initiatives and workstreams.
Provides input for capacity planning, including reporting of current manpower and forecasting of CRA capacity and needs, to provide efficient use of resources.
Work with CRAs, PLMS and other functions to ensure consistency of processes and protocol implementation across the country, to reduce variability and provide predictability.
Interacts with sites as needed to resolve site or CRA operational issues to meet commitments in a timely manner in coordination with the study CRM.
Attend local Investigator Meetings if requested to.
Interface with GCTO partners on clinical trial execution.
Escalates site performance issues to Head of Site Management and Monitoring.
People and Resource Management:
Manage CRA – career development, performance reviews, etc., including addressing low performance situations, and taking appropriate actions.
- Support and resolve escalation of issues from CRAs.
- Liaise with local HR and finance functions as required.
- Contribute to HQ capacity/resource planning activities to ensure efficient allocation of resources and work. Manage local conflicts between resource and work.
- Provides training, support and mentoring to the CRA to ensure continuous development.
- Ensures CRA compliance to corporate policies, procedures and quality standards

Qualifications, Skills & Experience:

CORE Competency Expectations:

Ability to work independently and in a team environment
Excellent people management, time management, project management and organizational skills
History of strong performance
Skills and judgment required to be a good steward/decision maker for the company
Fluent in Local Language and business proficient in English (verbal and written)
Excellent working knowledge of all applicable ICH/GCP regulations and Good Documentation Practices and ability to work within these guidelines
Expertise in and excellent working knowledge of core trial management systems and tools

Behavioral Competency Expectations:

High emotional intelligence
Strong leadership skills with proven success in people management
Excellent interpersonal and communication skills, conflict management
Demonstrated ability to build relationships and to communicate effectively with external customers (e.g. sites and investigators)
Influencing skills

Experience Requirements:

Required:

Minimum of 5 years’ experience within Clinical Research
Minimum of 3 years’ experience as CRA monitoring clinical trials
Line management experience preferred or at the minimum team leader experience

Educational Requirements:

Required:

Bachelor’s degree in Science

Preferred:

Advanced degree, (e.g. BA/BS or higher) with a strong emphasis in science and/or biology

#eligibleforERP

#clinicaltrialjobs

Required Skills:

Clinical Research, Clinical Research Methods, Clinical Study Management, Clinical Study Protocols, Clinical Trials Marketing, Conflict Management, Continuous Development, Data Reporting, Ethical Standards, Global Coordination, ICH GCP Guidelines, Liaison Work, Multiple Therapeutic Areas, Organizational Leadership, People Leadership, People Management, Performance Monitoring, Regulatory Compliance, Resource Allocation, Resource Deployment, Resource Planning, Site Operations, Situational Leadership, Standards Compliance, Study Monitoring

Preferred Skills:

Cardiovascular Research, Infectious Disease, Infectious Disease Research, Line Management, Task Organization, Team Organization, Time Management, Vaccine Research

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:

$142,400.00 - $224,100.00

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:

No relocation

VISA Sponsorship:

Travel Requirements:

50%

Flexible Work Arrangements:

Remote

Shift:

Not Indicated

Valid Driving License:

Hazardous Material(s):

n/a

Job Posting End Date:

10/23/2026

*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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