Shanghai, Shanghai, China
7 days ago
Sr. Clinical Trial Coordinator, GCTO

Job Description

Responsibilities include, but are not limited to:

• Study Payments:

Collaborate with finance/budgeting representatives for:

o Calculate and execute payments (to investigator sites, vendors)
o Handle Study accrual
o Ensure adherence to financial and compliance procedures
o Monitor and track adherence and disclosures,
o Maintain tracking tools

• Trial and site administration:

o Ensure collation and distribution of study tools and documents
o Update payment system and trackers

• Document management:
o Prepare documents and correspondence
o Collate, distribute/ship, and archive clinical documents

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Current Contingent Workers apply HERE

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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):

Required Skills:

Adaptability, Adaptability, Clinical IT, Clinical Research, Clinical Research Ethics, Clinical Site Monitoring, Clinical Study Management, Clinical Testing, Clinical Trial Compliance, Clinical Trial Documentation, Data Analysis, Document Management, Drug Development Research, Good Clinical Data Management Practice (GCDMP), Interpersonal Relationships, Medical Records Management, Monitoring and Evaluation (M&E), New Technology Integration, Nursing, Product Testing, Project Management, Project Management Tracking, Regulatory Compliance, Regulatory Compliance Consulting, Regulatory Training {+ 4 more}

 Preferred Skills:

Job Posting End Date:

07/31/2025

*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.


Requisition ID:R353748

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