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Clinical Trial Disclosure Associate - Remote
Company | Proclinical Staffing |
Address | Chicago, IL, United States |
Employment type | CONTRACTOR |
Salary | |
Category | Medical Equipment Manufacturing,Biotechnology Research,Pharmaceutical Manufacturing |
Expires | 2023-06-07 |
Posted at | 1 year ago |
Proclinical is seeking a remote Clinical Trial Disclosure Associate for a top pharmaceutical company.
Must be eligible to work in the US.
Job Responsibility
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies.
Proclinical Staffing is an equal opportunity employer.
INDOA
Must be eligible to work in the US.
Job Responsibility
- Exhibits a moderate level of technical competencies and requires a low level of counsel and guidance.
- Communicates deliverables, process and timelines effectively across functional areas and within department to accomplish project objectives.
- 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.).
- Coordinates the review, approval, and other appropriate functions.
- Continually trains/is compliant with all current SOPs & work instructions.
- Responsibilities will be focused on supporting EU CTR applications and documentation. Familiarity with clinical study and site start up documentation is preferred.
- 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.
- Identifies conflicts and resolves or elevates them to management to ensure resolution.
- 2 years of writing experience preferred
- Attention to detail. Find and correct errors in spelling, punctuation, grammar, consistency, clarity and accuracy.
- Ability to shift daily priorities, meet deadlines, ask questions
- Works well in a global, team environment
- Project management experience preferred
- Proficient with major Microsoft suite programs and other pharma systems
- 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
- Bachelor's degree required, preferably in a health or biological science field
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies.
Proclinical Staffing is an equal opportunity employer.
INDOA
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