Job Description

Company Description

ProPharma Group is an industry leading, single source provider for regulatory compliance, pharmacovigilance, and medical information services across the full development lifecycle for pharmaceutical, biotechnology, and medical device companies. Operating around the world with offices in Australia, Canada, Germany, Japan, the Netherlands, Sweden, United Kingdom, and the United States, ProPharma Group’s fully integrated service offerings will provide clients with a comprehensive suite of global support services that are required to be competitive in today’s dynamic markets. We build successful long-term relationships with clients by providing leading industry knowledge, experience, and proven processes.

Job Description

The Medical Writer reports to the Sr. Vice President, Clinical Services and provides medical writing and publication writing support to ProPharma Group clients.

Essential Functions Include

• Creates writing deliverables that include, but may not be limited to:
• clinical study protocols and clinical protocol amendments;
• clinical study reports;
• ND submissions and annual reports;
• Integrated summary reports;
• NDA and (e)CTD submissions;
• investigator brochures, as well as;
• clinical journal manuscripts, clinical journal abstracts, and client presentations.
• Reviews statistical analysis plans and table/figure/listing specifications for appropriate content, and for grammar, format, and consistency.
• Interacts with department head and staff members in data management, biostatistics, regulatory affairs, and medical affairs as necessary to produce writing deliverables.
• Adheres to established regulatory standards, including but not limited to ICH-E3 guidelines, as well as Company Standard Operating Procedures, client standards, and Company and/or client approved templates when completing medical writing projects, on-time and on-budget.
• Coordinate quality control reviews of documents and maintaining audit trails of changes.
• May perform quality control (QC) review if requested by supervisor (e.g., QC in-text tables against statistical tables, verify titles in standard table of contents, paginate a document, etc.).
• Provide input on data analysis planning and interpretation.
• Assist with project-related administrative tasks (e.g., copying of data and insertion into tabbed binders, replacing old data with new data, etc.).
• Demonstrates knowledge of regulatory submission requirements and processes.
  

Qualified Candidates Must Have

Qualifications

• Bachelor’s degree in the life sciences; MS or PhD preferred.
• Minimum of 2 years of experience in the writing regulatory documents for pharmaceutical, biologic or medical device companies.
• Expert word processing skills in MS Word, including proficiency with tables, graphs, and figures are required.
• Must be able to work in a collaborative team environment.
• Strong computer skills, project management skills, and a high attention to detail.
• Excellent demonstrable understanding of ICMJE and GPP guidelines and regulations required.
• Ability to write presentations and articles for peer reviewed publications that conform to prescribed style and format.
• Knowledge of internet software, spreadsheet software, word processing software, graphics software (e.g., PowerPoint), bibliographic software e.g. EndNote) and any other applicable software as may be needed by the job from time to time as it changes.
• Proven team player who can focus and continuously reinforce efforts to meet timelines.
  

Additional Information

All candidates must be legally eligible to work in the United States.

We are an equal opportunity employer. M/F/D/V

***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.*** more