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Related keywords
- Clinical Trial Associate
- Lead Clinical Trial Associate
- Clinical Trial Management Associate
- Clinical Trial Payments Associate
- Senior Clinical Trial Associate
- Global Clinical Trial Associate
- Regional Clinical Trial Associate
- Associate Clinical Trial Manager
- Clinical Trial Supply Associate
- Clinical Trial Disclosure Associate
Clinical Trial Associate Jobs
Company | Randstad Life Sciences US |
Address | Raleigh-Durham-Chapel Hill Area, United States |
Employment type | FULL_TIME |
Salary | |
Category | Pharmaceutical Manufacturing |
Expires | 2023-09-07 |
Posted at | 9 months ago |
12+ Month Contract
FULLY REMOTE
Responsibilities:
- Familiarity with clinical study and site start up documentation is preferred.
- Continually trains/is compliant with all current SOPs & work instructions.
- Responsibilities will be focused on supporting EU CTR applications and documentation.
- Exhibits a moderate level of technical competencies and requires a low level of counsel and guidance.
- Identifies conflicts and resolves or elevates them to management to ensure resolution.
- Communicates deliverables, process and timelines effectively across functional areas and within department to accomplish project objectives.
- Coordinates the review, approval, and other appropriate functions.
- Completes activities to assist in ensuring timely disclosure of accurate, consistent, aligned and complete information globally.
- Responsibilities will vary based upon business need. May support global study registrations, writing scientific study results, protocol/result lay summaries, or anonymizing clinical documents for public disclosure by regulatory agencies.
- Holds team members accountable to agreed-upon project dates. Negotiates with functional areas on project outcomes and deliverables to meet conflicting demands (time, deliverables, etc.).
Experience / Qualifications:
- Works well in a global, team environment
- Attention to detail.
- 2 years of writing experience preferred
- Bachelor's degree required, preferably in a health or biological science field
- Ability to shift daily priorities, meet deadlines, ask questions
- 2-4 yrs experience in clinical trial registries, regulatory agency transparency or drug development with a clinical research, quality or regulatory background, preferably in a pharma environment
- Find and correct errors in spelling, punctuation, grammar, consistency, clarity and accuracy.
- Proficient with major Microsoft suite programs and other pharma systems
- Project management experience preferred
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