Clinical Trial Assistant, GCTO

Job Description

The CTA is an administrative support role for clinical trials. The role responsibilities include but not limited to the following activities:
Basically：

• Safety reports distribution and tracking.
• TMF support for country level document uploading to eTMF, assist with eTMF reconciliation, CDA collection, etc.
• Support HGRAC site filing documents collection and archiving.
• Coordinate with vendor for office supply purchasing, trial related documents printing and translation activity.
• Responsible for ABAC (Anti-Bribery and (Anti-)Corruption) check
• On site support for investigator meeting.
• Support CRM for tracker maintenance and run report from various systems and other activities based on CRM’s requirement.
• Contribute to CTA team knowledge by acting as mentor and/or sharing best practices, leading initiatives as required.
• Using IT technology to develop tool or work out solution to increase work efficiency and improve work accuracy will be preferred.

For the senior position:

• Take initiatives or POC and have leadership to support CTA managers or SMEs on process management or internal and external stakeholder management.

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:

No relocation

VISA Sponsorship:

No

Travel Requirements:

No Travel Required

Flexible Work Arrangements:

Not Applicable

Shift:

Not Indicated

Valid Driving License:

No

Hazardous Material(s):

N/A

Required Skills:

Adaptability, Adaptability, Anti-Bribery and Corruption (ABC), Business Management, Clinical Information Systems, Clinical IT, Clinical Research, Clinical Research Ethics, Clinical Site Management, Clinical Site Monitoring, Clinical Study Management, Clinical Testing, Clinical Trial Compliance, Data Analysis, Drug Development Research, Emergency Care, Good Clinical Data Management Practice (GCDMP), Interpersonal Relationships, IT Systems Development, Management Process, New Technology Integration, Organizational Management (OM), Project Management, Regulatory Compliance, Regulatory Training {+ 5 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:R353378