772 matching jobs for “Senior Clinical Research Associate”

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Pfizer

Senior Clinical Research Associate

Taipei, Taiwan

Full time
Regular

The Senior Clinical Research Associate is responsible for the site management, site monitoring and close-out of assigned clinical trials …

Added Oct 16, 2026

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Pfizer

Senior Clinical Research Associate

Istanbul, Turkey

Full time
Regular

… and database release activities, and maintaining strong engagement with investigators and site staff. The Senior Clinical Research Associate works closely with Site Care Partners and study team members throughout study start-up, execution, and …

Added Oct 16, 2026

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Bristol-Myers Squibb

Senior Clinical Research Associate

Taipei - TW

Full time
Regular

… to this email. To check your application status, please login to your Candidate Home Account. R1606700 : Senior Clinical Research Associate

Added Oct 15, 2026

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Bristol-Myers Squibb

Senior Clinical Research Associate

Taipei - TW

Full time
Regular

… • Bachelor’s degree required, preferably within life sciences or equivalent Experience: • Senior Clinical Research Associate: 5 years of monitoring experience. Demonstrates leadership attributes and capability to take on …

Added Oct 15, 2026

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Bristol-Myers Squibb

Senior Clinical Research Associate

Taipei - TW

Full time
Regular

Added Oct 15, 2026

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Bristol-Myers Squibb

Senior Clinical Research Associate

Taipei - TW

Full time
Regular

… to this email. To check your application status, please login to your Candidate Home Account. R1606697 : Senior Clinical Research Associate

Added Oct 15, 2026

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IQVIA Holdings

Senior Clinical Research Associate

London, United Kingdom

… 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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Merck (MSD)

Senior Associate, Clinical Research

IND - Haryana - Gurgaon (Vatika Towers)

Senior Associate, Clinical Research Responsibilities include, but are not limited to: • Trial and site …

Added Oct 16, 2026

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Merck (MSD)

Senior Clinical Research Associate

POL - Mazowieckie Wojewodztwo - Warsaw (Trade Center)

If you want to: Join a multi-award-winning leading biopharmaceutical company Be part of growing team of Clinical Research Associates Use new technology and smart monitoring tools Have flexibility of work and good …

Added Oct 16, 2026

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IQVIA Holdings

(Senior) Clinical Research Associate

Durham, North Carolina, United States +3 locations 2 postings

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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IQVIA Holdings

Senior Clinical Research Associate

Reading, United Kingdom

Added Oct 15, 2026

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IQVIA Holdings

Senior / Clinical Research Associate

Kuala Lumpur, Malaysia

… with a variety of colleagues and customers . You will need to have a good knowledge of applicable clinical research regulatory requirements. Qualifications: University degree in scientific discipline or healthcare …

Added Oct 15, 2026

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IQVIA Holdings

Senior / Clinical Research Associate

Sydney North, New South Wales, Australia +1 location

Added Oct 15, 2026

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Bristol-Myers Squibb

Clinical Research Associate

Otemachi-JP

Full time
Regular

… Site Initiation Visitに関連した資料の準備を支援する場合がある日本の要件に基づき、データベースロックの期限遵守に向けた調整を支援する場合があるシニアレベルの期待事項（Senior Clinical Research Associate に適用）施設レベルおよび国レベル双方において、潜在的な問題を主体的に特定・解決する Clinical Trial Managerおよび／またはLine managerと連携し、より複雑な課題の解決を支援する …

Added Oct 15, 2026

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IQVIA Holdings

Senior Clinical Research Associate

Amsterdam, The Netherlands

… data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward. Clinical FSP Business IQVIA clinical FSP business is unique. Our teams are dedicated to a single sponsor partner, …

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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Thermo Fisher Scientific

FSP Clinical Research Associate II/Senior Clinical Research Associate - Czechia

Remote, Czechia

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

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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IQVIA Holdings

(Senior) Clinical Research Associate, IQVIA

Durham, North Carolina, United States

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

Added Oct 15, 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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Merck (MSD)

Senior Associate, Clinical Research

IND - Haryana - Gurgaon (Vatika Towers)

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Key Skills · employer excerpt

• Fluent in Local Languages and business proficient in English (verbal and written) and
excellent communication skills
• Good understanding of Global, Country/Regional Clinical Research Guidelines and ability to
work within these guidelines.
• Hands on knowledge of Good Documentation Practices

14 more in the full description below.

About this opportunity

Original employer description

Job Description

Senior Associate, Clinical Research

Responsibilities include, but are not limited to:

• Trial and site administration:

o Track (e.g. essential documents) and report (e.g. Safety Reports)

o Ensure collation and distribution of study tools and documents

o Update clinical trial databases (CTMS) and trackers

o Clinical supply & non-clinical supply management, in collaboration with other country

roles

o Manage Labeling requirements and coordinate/sign translation change request, in

collaboration with other country roles (if applicable)

• Document management:

o Prepare documents and correspondence

o Collate, distribute/ship, and archive clinical documents, e.g. eTMF

o Assist with eTMF reconciliation

o Execute eTMF Quality Control Plan

o Update manuals/documents (e.g., patient diaries, instructions)

o Document proper destruction of clinical supplies.

o Prepare Investigator trial file binders

o Obtain translations of documents

• Regulatory & Site Start-Up responsibilities: Collaborate with other country roles to:

o In a timely manner, provide to and collect from investigators forms/lists for site

evaluation/validation, site start-up and submissions

o Obtain, track and update study insurance certificates

o Support preparation of submission package for IRB/ERC and support regulatory

agencies submissions.

o Publish study results for GCTO and RA where required per local legislation

• Budgeting, Agreement and Payments:

Collaborate with finance/budgeting representatives for:

o Develop, control, update and close-out country and site budgets (including Split site

budget)

o Develop, negotiate, approve and maintain contracts (e.g. CTRAs)

o Track and report contract negotiations

o Update and maintain contract templates (in cooperation with Legal Department)

o Calculate and execute payments (to investigators, vendors, grants)

o Ensure adherence to financial and compliance procedures

o Monitor and track adherence and disclosures

o Maintain tracking tools

o Obtain and process FCPA documentation in a timely manner

Meeting Planning:

o Organize meetings (create & track study memos/letters/protocols)

o Support local investigator meeting

Key Skills:

• Fluent in Local Languages and business proficient in English (verbal and written) and

excellent communication skills

• Good understanding of Global, Country/Regional Clinical Research Guidelines and ability to

work within these guidelines.

• Hands on knowledge of Good Documentation Practices

• Good IT skills (Use of MS office, use of some clinical IT applications on computer) and ability

to adapt to new IT applications. Strong MS Excel skills required.

• ICH-GCP Knowledge appropriate to role

• Excellent negotiation skills for CTCs in finance area

• Effective time management, organizational and interpersonal skills, conflict management

• Effective communication with external customers (e.g. sites and investigators)

• High sense of accountability / urgency. Ability to set priorities and handle multiple tasks

simultaneously in a changing environment

• Works effectively in a matrix multicultural environment. Ability to establish and maintain

culturally sensitive working relationships.

• Demonstrates commitment to Customer focus, both internally and externally.

• Able to work independently

• Proactive attitude to solving problems / proposing solutions

• Positive mindset, growth mindset

Additional location(s) Compensation Information:

Required Skills:

Accountability, Accountability, Analytical Problem Solving, Budget Development, Clinical Data Management, Clinical IT, Clinical Research, Clinical Trial Compliance, Clinical Trial Documentation, Clinical Trial Management, Clinical Trials Monitoring, Clinical Trials Operations, Clinical Trial Support, Conflict Management, Contract Processing, Customer Centricity, Data Analysis, Decision Making, Documentation Preparation, Document Management, Drug Regulatory Affairs, Good Clinical Practice (GCP), Growth Mindset, ICH GCP Guidelines, Independent Thinking {+ 9 more}

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

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:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Not Applicable

Shift:

Valid Driving License:

Hazardous Material(s):

Job Posting End Date:

10/22/2026

*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.

Why this result? · Employer labels

All keywords in title

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