Clinical Trial Assistant
About The Position
The Clinical Trial Assistant is a member of the clinical trial team supporting delivery of clinical studies within the sponsor. The CTA will support the study team to ensure the operational deliveries are executed then the expected timeline, approved budget, and at high quality from protocol development through study setup, maintenance, close out and study archiving. The CTA supports the study team in delegated activities and provides technical, administrative and logistical support to ensure efficient execution of clinical trials in line with ICH/GCP sponsor SOP's and regulatory regulations.
Requirements
- High school or GED with four years relevant experience.
- At least 1 year experience as a CTA, CRC, or other role in clinical trials.
- Proven organizational and presentation skills
- Ability to manage multiple tasks with meticulous attention to detail
- Quick learner and team player
- Excellent written and verbal communication skills
- Computer proficiency in Microsoft Word, Excel, PowerPoint and Outlook
- Good knowledge of the ICH/GCP
Nice To Haves
- Bachelor's degree or above (Life Sciences preferred) or certification in a related health profession (i.e. nursing, medical or laboratory technology) from an accredited institution is preferred.
- Oncology experience a huge plus!
Responsibilities
- Lead the setup of electronic Trial Master File (eTMF) system and clinical trial management (CTMS). Ensure information is updated during the study per ICH/GCP and sponsor SOP's
- Create and maintain communication platforms (i.e. MS Teams, SPOL, group e-mail list) for the study team
- Control systems access for assigned studies but not limited to IxRS, EDC, CT's, and eTMF
- Support clinical trial registration and disclosure on websites per applicable regulatory requirements
- Responsible for overall TMF status. Guide study team members on the eTMF/paper TMF document transfer and archival. Lead the quality check (QC) per the TMF plan. Help draft TMF plan
- Facilitate finance related activities such as sign off, IO and PO setup, processing invoices, track accruals and budget for maintenance and reconciliation for sites and third-party vendors
- Support oversight of monitoring visit report review. Activities include updating MVR trackers and overseeing MVR review metrics
- May support data oversight and reconciliation efforts vendor systems, SAEs, protocol deviations and more as needed per study
- Coordination and tracking of clinical supplies
- Coordinate and arrange internal and external meetings, including but not to study team meetings, vendor defense meetings, investigator meetings, and committee review meeting take meeting minutes as needed.
- Compile and maintain the clinical trial related lists and logs, including but not limited to study document version tracker, decision risk log, contact list, Q&A log, vendor list, and specific training log.
- Draft and distribute newsletters communications Asia materials to internal and external stakeholders
- Complete delegated tasks during audit and inspection by regulatory authorities
Benefits
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
High school or GED
