Associate Clinical Trial Management

Responsibilities:

1. Support study feasibility activities and perform database/web searches for sites as needed.
2. Work closely with the Site Start Up (SSU) and ensure all study related regulatory and financial documents are collected and reviewed in support of study activation.
3. Organize and maintain project working files and track critical documents. Report discrepancies to the appropriate clinical team member in a timely manner.
4. Reconcile and transmit all essential documentation to CDIC as per Forest policy.
5. Track and assist with processing site/vendor payments. Follow up on any issues as required.
6. Collect and track patient enrollment information and update study management reports as necessary.
7. Participate in testing of specifications and edit checks for internal (i.e. electronic data capture (EDC) and external (e.g. Interactive Voice/Web Response Systems (IVRS/IWRS), laboratory vendors) systems.
8. Assist senior team members with in the planning, preparation, and on-site support of investigators meetings.
9. Generate reports in various applications to assist the Clinical Scientist to perform clinical data review.
10. Assist with ongoing data review and discuss comments with the clinical study team as needed.
11. Assist with the preparation and distribution of meeting agendas and minutes. Actively participate in team meetings.
12. Provide input and support in the development and distribution of monthly site newsletters.
13. Support the Regional Site Managers by providing study related information and supplies, as requested.
14. Communicate with IRBs and outside vendors to provide information and/or resolution to specific requests/issues.
15. Support and correspond with sites to identify site specific needs (e.g. order and track study drug/other trial related supplies).


QUALIFICATIONS:

Associate degree or higher preferred

1-2 year relevant experience in pharmaceutical industry or CRO

Experience supporting clinical trials preferreD

Basic knowledge of drug development and FDA GCP/ICH regulatory guidelines is a plus
Proficiency with Microsoft Word, Microsoft PowerPoint, Microsoft Outlook, and Adobe Acrobat
Strong skills with Microsoft Excel required
Experience using electronic data capture (EDC) systems is a plus