Spclst, Clin. Operations
Spclst, Clin. Operations
Employer Active
Job Alert
You will be updated with latest job alerts via email
Share
Job Alert
You will be updated with latest job alerts via email
Job Description
Job Description
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 CRMs 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:
RegularRelocation:
No relocationVISA Sponsorship:
NoTravel Requirements:
No Travel RequiredFlexible Work Arrangements:
Not ApplicableShift:
Not IndicatedValid Driving License:
NoHazardous Material(s):
N/ARequired Skills:
Clinical IT Clinical Research Clinical Study Management Clinical Trial Compliance Clinical Trials Drug Development Research Electronic Trial Master File Good Clinical Data Management Practice (GCDMP) Project Management Regulatory CompliancePreferred Skills:
Administrative Support Document Administration Onsite SupportJob Posting End Date:
12/31/2025*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
Employment Type
Full-Time
