Job Details

ID #21633694
State New Jersey
City Lawrencetownship
Job type Contract
Salary USD TBD TBD
Source TSR Consulting Services, Inc.
Showed 2021-10-24
Date 2021-10-23
Deadline 2021-12-21
Category Et cetera
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Medical Writer

New Jersey, Lawrencetownship, 08648 Lawrencetownship USA

Vacancy expired!

Our client, a leading pharmaceutical company is hiring a Medical Writer on a contract basis.

Work Location:

Lawrence Township, NJ

Required Skills

Manager, Worldwide Scientific Content and US Market Capabilities

PhD/MD/PharmD in a relevant scientific discipline or MS / BS with a minimum of 3 years (MS) to 5 years (BS) in pharmaceutical regulatory documentation, or equivalent, and good understanding of requirements for regulatory submission documents. In addition, (i) demonstrated strong writing skills as evidenced by good quality writing in pharmaceutical regulatory documentation and/or publications in peer-reviewed journals, (ii) good understanding of global pharmaceutical drug development and requirements for submission of regulatory dossiers to global health authorities, (iii) demonstrated ability to manage timelines and quality of work using strong organizational, communication, facilitation and interpersonal skills in a cross-functional team, (iv) working knowledge of a document management system and basic knowledge of document publishing process, (v) analyzed and interpreted complex data from a broad range of scientific disciplines.

Coordinate and author regulatory documents (e.g. phase I/II clinical study reports, Investigators Brochure) ensuring the coordination and integration of the scientific, medical and regulatory input from development team members.2. When assigned as Lead Writer, ability to lead other writers, including developing strategies/ plans and managing projects, in order to complete multiple documents for regulatory submissions.3. Demonstrate mastery of complex writing assignments (e.g., Phase III CSRs, CSS, CSE, Background Packages, etc.) across therapeutic areas or multiple projects.4. Participate in relevant filing subteam(s) and ensure effective planning and management of timelines for all components of assigned documents.5. Lead or co-lead (with Doc Lead) teams to define content and data displays for CSR prototypes and shells. 6. Able to collaborate with project team to respond to health authority questions, requests, etc.7. Provide departmental management with adequate information to help assess resource needs.
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