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

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Amgen

Senior Associate, Quality Compliance (Analytics)

India - Hyderabad

Full time
Regular

Role Name: Senior Associate Quality Compliance (Analytics) Department Name: R&D Quality Role GCF: 4 ABOUT AMGEN Amgen harnesses the …

Added Oct 15, 2026

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Vertex Pharmaceuticals

Strategic Sourcing Associate Director

Boston, Massachusetts, United States

Full time
Regular

Pay posted by employer$145,600–$218,400

General Summary: As the Associate Director of Strategic Sourcing for Cell and Gene Therapy (CGT) Raw Materials, you will be part of a …

Added Oct 18, 2026

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Merck (MSD)

Associate Director, Global Marketing - Obesity

Rahway, New Jersey, United States +1 location

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

… value creation for patients, healthcare professionals, healthcare customers, and the enterprise. The Associate Director, Global Marketing – Obesity will operate at the intersection of strategy, asset development, and …

Added Oct 16, 2026

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IQVIA Holdings

Associate Consultant - Onsite Deployment Unit

Porto Salvo, Portugal

Analyse secondary data and desk market research to identify key findings and trends Perform quantitative or qualitative analysis to support client …

Added Oct 15, 2026

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Thermo Fisher Scientific

Project Support Associate, Client Services

Vacaville, California, United States

Pay posted by employer$23.04–$34.56 per hour

… or helping find cures for cancer. Join our team at Thermo Fisher Scientific and contribute to advancing clinical research. As a Project Support Associate, you'll support clinical trials by managing project documentation, …

Added Oct 16, 2026

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Johnson & Johnson

Sales Associate West London Endomech

Wokingham, United Kingdom

Sales Associate, 12 months fixed term contact – J&J Medtech Surgery Endomechanical & Energy, East of England Fuelled by …

Added Oct 18, 2026

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Merck (MSD)

Associate Principal Scientist, Regulatory Liaison

USA - Pennsylvania - North Wales (Upper Gwynedd) +1 location

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

Brief Description of Position The Regulatory Affairs Headquarters Associate Principal Scientist supports products in the Vaccine and Infectious Disease (VID) therapeutic area as part …

Added Oct 16, 2026

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Merck (MSD)

Associate Specialist, Operations (Onsite)

Rahway, New Jersey, United States

Pay posted by employer$71,900–$113,200

… Pilot Plant is a GMP (Good Manufacturing Practices) manufacturing facility in the Small Molecule Process Research and Development (SM PR&D) organization. The SSO pilot plant enables gain of critical internal experience …

Added Oct 18, 2026

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Merck (MSD)

Associate Specialist, Operations (Onsite)

Rahway, New Jersey, United States

Pay posted by employer$71,900–$113,200

Added Oct 18, 2026

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IQVIA Holdings

Associate, Market Access Consulting (Brazil)

São Paulo, Brazil

… and actionable recommendations for clients • Conduct primary (qualitative) and secondary (quantitative) research on markets, payers, physicians, patients, and competitive products to identify key findings for client …

Added Oct 15, 2026

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Johnson & Johnson

Associate Scientist I, Discovery-Oncology

Beerse, Belgium

… compliance with regulatory requirements. You will contribute to in vivo and ex vivo studies across multiple research programs and contribute to the advancement of innovative therapies. Specifically, you will establish and …

Added Oct 18, 2026

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Labcorp Holdings

Sample Handling Associate I

Bengaluru, India

Full time
Regular

… Minimum Qualifications Bachelor’s Degree in Science Preferred Qualifications 6 months work experience in a clinical research industry. Master's Degree in Science. Additional Job Standards Strong attention to detail Ability …

Added Oct 16, 2026

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IQVIA Holdings

Associate Manager , Talent Acquisition

Bengaluru, India

… managers and clients IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and …

Added Oct 15, 2026

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IQVIA Holdings

Medical Advisor/Associate Director (Rheumatology)

Beijing, China +3 locations

… (IDB), and/or Case Report Forms (CRFs). Provides therapeutic area/indication training for the project clinical team. Attends and presents at Investigator Meetings. Performs review and clarification of trial-related …

Added Oct 15, 2026

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Becton Dickinson

Associate Territory Manager - Columbus, OH

Columbus, Ohio, United States +1 location

Pay posted by employer$66,700–$106,700 USD

Overview: The Associate Territory Manager (ATM) is primarily responsible for providing field level support to physicians and other …

Added Oct 27, 2026

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IQVIA Holdings

Associate Territory Representative - North & West Chicagoland

North Chicago, Illinois, United States +1 location

Pay posted by employer$55,000–$60,000 per year

… assigned geography Educate physicians, nurse practitioners, physician assistants, and clinic staff on the clinical and patient benefits of products Drive new prescription volume by converting prescribers and expanding …

Added Oct 15, 2026

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IQVIA Holdings

Associate Territory Representative - Colorado Front Range

Denver, Colorado, United States

Pay posted by employer$55,000–$60,000 per year

Added Oct 15, 2026

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IQVIA Holdings

Associate Territory Representative - Buffalo - Rochester - Syracuse

Buffalo, New York, United States +2 locations

Pay posted by employer$55,000–$60,000 per year

Added Oct 15, 2026

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IQVIA Holdings

Associate Territory Representative - Connecticut - Western Massachusetts

Hartford, Connecticut, United States +1 location

Pay posted by employer$55,000–$60,000 per year

Added Oct 15, 2026

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Bristol-Myers Squibb

Associate Director, Translational Medicine, Neuroscience

Princeton - NJ - US +3 locations

Full time
Regular

Pay posted by employer$184,060–$223,036

… area Leads small and large collaborations with academia and industry partners to identify biobanks, clinical trials and existing databases to collate multi-parameter genomic, immune and clinical datasets to mine for …

Added Oct 15, 2026

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Merck (MSD)

Associate Specialist, Operations (Onsite)

Rahway, New Jersey, United States

Pay posted by employer$71,900–$113,200

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Required Experience and Skills · employer excerpt

Strong communication skills to discuss technical problems and a collaborative mindset to interface with cross-functional teams.
A strong mechanical aptitude.
Proficiency in technical writing and the use of word processing, spreadsheet, graphing, and presentation software.
This role requires working on 8-hour shifts that rotate between 1st and 2nd shift on alternating weeks throughout the year. Onsite presence is required five days a week. Occasional overtime work may be required based on business needs.

About this opportunity

Original employer description

Job Description

The Small Scale Organics (SSO) Pilot Plant is a GMP (Good Manufacturing Practices) manufacturing facility in the Small Molecule Process Research and Development (SM PR&D) organization. The SSO pilot plant enables gain of critical internal experience with scale-up of manufacturing GMP steps, demonstration of new manufacturing technology/processes, training opportunities for improved manufacturing process development, and seamless technology transfer to commercial sites.

The SSO Operations Specialist will provide hands on assistance for daily production activities while ensuring compliance with Safety & Environmental (S&E) and current Good Manufacturing Practices (cGMPs) requirements to meet SSO objectives and customer requirements. The position is responsible for implementing actions to meet S&E and GMP requirements. This position is also responsible for ensuring facility readiness for batch processing and shares accountability for the building performance. Ultimately, this position is expected to work cooperatively with the SSO leadership team and SSO partners to drive overall success and performance of the building, and ultimately strong support for the overall SM PR&D pipeline.

Responsibilities:

Under the scientific direction of a facility lead, the Operations Specialist will participate in equipment setups, raw material sampling and subdivisions, solution preparations, batch processing planning and execution at a pilot scale, process knowledge capture, and troubleshooting equipment with the aim of advancing process development, aiding technology development, and supplying Active Pharmaceutical Ingredient (API) for clinical use and drug product development. This will involve handling of a variety of reagents, solvents, and active pharmaceutical ingredients during “wet chemistry” operations (performing chemical reactions, extractions, distillations, crystallizations, filtration, drying, etc.) Also, dry powder processing (e.g., dry milling).
Ensure processes are run within the capability constraints of the facility.
Ensure facility readiness with respect to cleaning (including documentation and execution), batch execution, building housekeeping, and consumable inventory.
Provide input for incident root cause analysis, reporting, and action items.
Facilitate and drive building improvement projects and corrective/preventative action closures.
Provide input on process setups.
Provide regular feedback to peers to promote a continuous improvement mindset.
Collaborate with all building staff to share and align on best practices.
Actively investigate problem statements and safety observation reports (SORs) to promote fast and efficient closure.
As needed, safely perform High Risk Work involving hazardous energy control.
Identify and follow through on opportunities to improve building flexibility, efficiency, compliance, and safety.
Author lessons learnt and summary reports to capture knowledge gained.
Mentor and help train rotational and new employees.
This position’s primary focus is executing batch production work. Additional responsibilities include coordination, planning, documentation, and other facility improvement activities.

Position Qualifications:

Education Minimum Requirement:

Associate in Science, Associate in Applied Science (ideally in Process Technology), or higher degree in a relevant technical field of study with expected completion by June 2026 – or –
High School Diploma/GED plus at least four (4) years of relevant experience in Pharmaceutical, Chemical, Petrochemical or Food Processing/Manufacturing.

Required Experience and Skills:

Strong communication skills to discuss technical problems and a collaborative mindset to interface with cross-functional teams.
A strong mechanical aptitude.
Proficiency in technical writing and the use of word processing, spreadsheet, graphing, and presentation software.
This role requires working on 8-hour shifts that rotate between 1st and 2nd shift on alternating weeks throughout the year. Onsite presence is required five days a week. Occasional overtime work may be required based on business needs.

Preferred Experience and Skills:

Operations experience in pilot plant or manufacturing environment.
Understanding of/Experience with process scale-up of chemical processes, moving from the laboratory to the pilot scale.
Familiarity with the administration of cGMPs, Good Documentation Practices (GDPs), and S&E regulations as it pertains to pharmaceutical development.
Lean Six Sigma Training / Certification.

#MSJR

#eligibleforERP

#PRD

Required Skills:

Assembly Operations, Assembly Operations, Batch Production, Chemical Engineering, Chemical Processes, Equipment Troubleshooting, GMP Compliance, Good Manufacturing Practices (GMP), HR Programs, Lockout Tagout, Machinery Operation, Mechanical Aptitude, Petrochemistry, Pharmaceutical Manufacturing, Pharmaceutical Quality Assurance, Pilot Plant Operations, Process Chemistry, Process Technologies, Production Efficiencies, Production Scheduling, Safety Protocols, Shift Work, Spreadsheet Software, Teamwork, Technical Writing {+ 1 more}

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:

$71,900.00 - $113,200.00

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:

No relocation

VISA Sponsorship:

Travel Requirements:

No Travel Required

Flexible Work Arrangements:

Not Applicable

Shift:

1st - Day, 2nd - Evening

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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