Medical Writer Job at Aequor Technologies, Princeton, NJ

  • Aequor Technologies
  • Princeton, NJ

Job Description

*PIPELINE*
TITLE: Medical Writer

Must have 5 -7 years of experience.

POSITION SUMMARY:
The Medical Writer a ccountable for the timely delivery of high quality, regulatory-compliant documents including but not limited to protocols, IBs, clinical study reports, health authority briefing books and clinical summary documents for assigned program and ensures documents are delivered per corporate objectives, from planning through internal approval.

Responsibilities and Duties:
  • Responsible for the development of high quality clinical documents submitted to Regulatory Authorities (e.g. FDA and EMA) including Clinical Study Reports, Investigator Brochures, Protocols, Protocol Amendments, Briefing Documents, Health Authority responses, and clinical summary sections of Common Technical Documents (CTDs) in support of worldwide regulatory submissions.
  • Collaborates with Global Development Teams and Clinical Development to ensure alignment with program objectives.
  • Oversees and reviews medical writing deliverables assigned to contractors or other third party vendors.
  • Participates in Global Medical Writing initiatives on clinical development cross-functional teams.
  • Assists with development and implementation of Medical Writing processes improvement in line with SOPs.
  • Owns and updates assigned Medical Writing SOPs, as necessary.

Educational Requirements:
  • Bachelor's Degree in life science, health-related or pharmaceutical field, or the equivalent in experience. Advanced degree preferred.
Experience:
  • Minimum of 5 years combined experience in academic/clinical and/or industry setting writing clinical protocols, CSRs and/or medical and/or scientific documents.
  • Previous experience in Medical Writing in clinical drug development.
  • Familiarity with the regulatory submission process, ICH and GCP guidelines and recommendations.
  • Knowledge of template development, document management systems and requirements.
  • Strong working knowledge of Medical Writing requirements and document components.
  • Good interpersonal skills that involves working well in a team environment and the ability to lead others.
  • Strong PC skills including Medical Writing software, Windows and MS Office products specifically Word, Excel, MS Project, and PowerPoint (and any additional software packages utilized ).

Job Tags

For contractors, Worldwide

Similar Jobs

Department of State - Agency Wide

Foreign Affairs Officer Job at Department of State - Agency Wide

 ...the Office of the Assistant Secretary, Bureau of Educational and Cultural Affairs (ECA). The mission of ECA is to assist in the...  ...on timed sections only. Applicants submitting a RA request MUST attach supporting medical documentation signed by a licensed, treating... 

AHU Technologies Inc

Drupal Web Developer Job at AHU Technologies Inc

 ...Job Description: Short Description: Client requires the services of a contractor Web Developer with strong Drupal expertise to support the development, maintenance, and modernization of District government websites, including DC.gov and associated agency digital... 

Apex Systems

Data Business Analyst Job at Apex Systems

 ...OverviewThis role will own the end-to-end engagement, onboarding, and insights experience for partners consuming quality and operations data. The lead will translate business needs into clear reporting, metrics, and data flows, and ensure the underlying file-upload... 

Overhead Door Corporation

Director Operations - Installation Project Management - Relocation Job at Overhead Door Corporation

 ...installation programs Building and leading highperforming project management teams and scalable processes Owning a P&L and driving...  ...Role Summary Working closely with the VP of Sales, the Director of Operations is responsible for leading the endtoend execution... 

Katalyst CRO

Clinical Data Manager Job at Katalyst CRO

 ...Responsibilities Lead clinical data management activities for multiple complex studies, from study startup to database lock and final reporting.Develop and manage data management timelines for multiple projects, ensuring all milestones are met according to project plans...