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 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.
#R365634
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:
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 Compliance
Preferred Skills:
Administrative Support Document Administration Onsite Support
Job 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.
Job DescriptionThe 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...
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 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.
#R365634
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:
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 Compliance
Preferred Skills:
Administrative Support Document Administration Onsite Support
Job 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.
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