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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
Job Description
Proclinical is seeking a remote Clinical Trial Disclosure Associate for a top pharmaceutical company.
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.
Skills And Requirements
  • 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
If you are having difficulty in applying or if you have any questions, please contact Jackie Cerchio at (+1) 267-846-2026 or [email protected].
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