Clinical Trial Disclosure Associate
4 weeks ago
Are you passionate about advancing medical knowledge and improving human health? Do you have a strong background in clinical research and regulatory affairs? We're seeking a highly motivated and detail-oriented Clinical Trial Disclosure Associate to join our team at PSG Global Solutions Careers.
About the RoleAs a Clinical Trial Disclosure Associate, you will play a critical role in ensuring the accuracy and completeness of clinical trial registrations and results disclosures. You will work closely with our Senior Associate, CTD and Manager(s) of CTD to execute clinical drug trial registration and results disclosure postings in accordance with regulatory and Standard Operating Procedure (SOP) requirements.
Key Responsibilities- Assist in the execution of clinical drug trial registration and results disclosure postings
- Work closely with the Senior Associate, CTD and Manager(s) of CTD to ensure compliance with regulatory and SOP requirements
- Support the development and implementation of clinical trial registration and results disclosure strategies
To be successful in this role, you will need:
- A BS/BA degree from an accredited college or university in a health or biological science field
- 2+ years of clinical research experience or experience in a related area such as quality or regulatory
- Familiarity with ICH and GCP Guidelines and good organizational and communication skills
- Ability to prioritize roles and responsibilities daily and work well under deadline pressure in a team environment
At PSG Global Solutions Careers, we offer a dynamic and supportive work environment that fosters growth and development. As a Clinical Trial Disclosure Associate, you will have the opportunity to work with a talented team of professionals who are passionate about advancing medical knowledge and improving human health.
We are committed to providing our employees with the tools and resources they need to succeed in their roles. If you are a motivated and detail-oriented individual with a strong background in clinical research and regulatory affairs, we encourage you to apply for this exciting opportunity.
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