RESUME AND JOB
MSD
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:
RegularRelocation:
VISA Sponsorship:
Travel Requirements:
Flexible Work Arrangements:
Not ApplicableShift:
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.
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.
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MSD
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:
RegularRelocation:
VISA Sponsorship:
Travel Requirements:
Flexible Work Arrangements:
Not ApplicableShift:
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.
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.
Get personalized recommendations to optimize your resume specifically for Sr. Manager, Clinical Research. Takes only 15 seconds!
Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.
Answer 10 quick questions to check your fit for Sr. Manager, Clinical Research @ MSD.

No related jobs found at the moment.

© 2026 Pointers. All rights reserved.