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Sr. Manager, Clinical Research

MSD

Sr. Manager, Clinical Research

full-timePosted: Dec 5, 2025

Job Description

Categories: Pharmaceutical, Clinical Research, Oncology

Job Description

  • Clinical and Regulatory

    Strategy Development: Drive the clinical

    development, expand

    portfolio, and speed

    up registration;Get alignments with Global

    PDT and obtain

    CDRC/LDRC endorsement.

    Execution clinical &

    registration strategy

  • Protocol Development:Accountable for protocol

    development, approval

    and amendment of China

    stand alone phase I –III

    and PMC.

  • Clinical Trial Execution:Feasibility assessment;

    Medical monitoring

  • Regulatory Submission

    & Interaction:CSA application, pre-IND,

    IND, pre-NDA, NDA filing

    and approval.

  • Innovation &

    Scientific Engagement:MISP/OTSP studies

    o Scientific

    leadership; SIE(Scienti

    fic inputs engagement)

    etc.

    ; Publications

Required Skills:

Accountability, Accountability, Adaptability, Bioinformatics, Chromatography, Clinical Development, Clinical Medicine, Clinical Quality Management, Clinical Research, Clinical Study Design, Clinical Trial Planning, Clinical Trials, Clinical Trials Monitoring, Data Analysis, ICH GCP Guidelines, Investigation Procedures, Medical Writing, Non-Disclosure Agreements, Process Improvements, Regulatory Compliance, Regulatory Strategies, Risk Management, Scientific Research, Scopus, Strategic Planning {+ 3 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:

01/31/2026

*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.

Locations

  • Beijing, Beijing, China

Salary

Estimated Salary Rangemedium confidence

126,000 - 198,000 USD / yearly

Source: AI Estimation

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Clinical Researchadvanced
  • Clinical Trial Planningadvanced
  • Medical Writingadvanced
  • Strategic Planningadvanced
  • Regulatory Complianceadvanced
  • Clinical Trials Monitoringintermediate
  • ICH GCP Guidelinesadvanced

Required Qualifications

  • PhD or Master's in Clinical Medicine (at least 5-year medical school graduate) with postgraduate training in oncology or related major (degree)
  • Deep understanding of China regulatory environment and clinical development procedures (experience)
  • Previous experience in clinical research or clinical development including strategy development, medical monitoring, and protocol writing (experience)
  • Fluent in English and Chinese (verbal and written) (experience)

Responsibilities

  • Provide leadership in conducting early clinical research in China to broaden indications and support global drug development
  • Drive assigned programs towards product registration by developing study protocols
  • Engage key opinion leaders to support clinical research initiatives
  • Draft study reports and prepare dossiers for regulatory submission
  • Lead strategy development, medical monitoring, and protocol writing for clinical programs
  • Manage multiple projects with prioritization and deliver results under parallel tasks

Benefits

  • General: Opportunity to lead innovative clinical research impacting global drug development
  • General: Work in a dynamic environment at Merck's Beijing office (Wangjing Park)
  • General: Professional growth in oncology and clinical research with leadership responsibilities

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MSD logo

Sr. Manager, Clinical Research

MSD

Sr. Manager, Clinical Research

full-timePosted: Dec 5, 2025

Job Description

Categories: Pharmaceutical, Clinical Research, Oncology

Job Description

  • Clinical and Regulatory

    Strategy Development: Drive the clinical

    development, expand

    portfolio, and speed

    up registration;Get alignments with Global

    PDT and obtain

    CDRC/LDRC endorsement.

    Execution clinical &

    registration strategy

  • Protocol Development:Accountable for protocol

    development, approval

    and amendment of China

    stand alone phase I –III

    and PMC.

  • Clinical Trial Execution:Feasibility assessment;

    Medical monitoring

  • Regulatory Submission

    & Interaction:CSA application, pre-IND,

    IND, pre-NDA, NDA filing

    and approval.

  • Innovation &

    Scientific Engagement:MISP/OTSP studies

    o Scientific

    leadership; SIE(Scienti

    fic inputs engagement)

    etc.

    ; Publications

Required Skills:

Accountability, Accountability, Adaptability, Bioinformatics, Chromatography, Clinical Development, Clinical Medicine, Clinical Quality Management, Clinical Research, Clinical Study Design, Clinical Trial Planning, Clinical Trials, Clinical Trials Monitoring, Data Analysis, ICH GCP Guidelines, Investigation Procedures, Medical Writing, Non-Disclosure Agreements, Process Improvements, Regulatory Compliance, Regulatory Strategies, Risk Management, Scientific Research, Scopus, Strategic Planning {+ 3 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:

01/31/2026

*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.

Locations

  • Beijing, Beijing, China

Salary

Estimated Salary Rangemedium confidence

126,000 - 198,000 USD / yearly

Source: AI Estimation

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Clinical Researchadvanced
  • Clinical Trial Planningadvanced
  • Medical Writingadvanced
  • Strategic Planningadvanced
  • Regulatory Complianceadvanced
  • Clinical Trials Monitoringintermediate
  • ICH GCP Guidelinesadvanced

Required Qualifications

  • PhD or Master's in Clinical Medicine (at least 5-year medical school graduate) with postgraduate training in oncology or related major (degree)
  • Deep understanding of China regulatory environment and clinical development procedures (experience)
  • Previous experience in clinical research or clinical development including strategy development, medical monitoring, and protocol writing (experience)
  • Fluent in English and Chinese (verbal and written) (experience)

Responsibilities

  • Provide leadership in conducting early clinical research in China to broaden indications and support global drug development
  • Drive assigned programs towards product registration by developing study protocols
  • Engage key opinion leaders to support clinical research initiatives
  • Draft study reports and prepare dossiers for regulatory submission
  • Lead strategy development, medical monitoring, and protocol writing for clinical programs
  • Manage multiple projects with prioritization and deliver results under parallel tasks

Benefits

  • General: Opportunity to lead innovative clinical research impacting global drug development
  • General: Work in a dynamic environment at Merck's Beijing office (Wangjing Park)
  • General: Professional growth in oncology and clinical research with leadership responsibilities

Target Your Resume for "Sr. Manager, Clinical Research" , MSD

Get personalized recommendations to optimize your resume specifically for Sr. Manager, Clinical Research. Takes only 15 seconds!

AI-powered keyword optimization
Skills matching & gap analysis
Experience alignment suggestions

Check Your ATS Score for "Sr. Manager, Clinical Research" , MSD

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score

Tags & Categories

MSDMerckPharmaPharmaceuticalClinical ResearchOncology

Answer 10 quick questions to check your fit for Sr. Manager, Clinical Research @ MSD.

Quiz Challenge
10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.