Job Description

12 month contract

The hours per week may start at closer to 20 hours/week and then ramp up to 30 or 40 hours based on how quickly training is completed and how independently the writer is able to work.

Looking for someone at an Associate Director level of medical writing with minimum of 3 years in pharma space with phase 1 pharmacology experience with protocols.

Position Summary: The primary responsibilities of an Associate Director Medical Writer at include, but are not limited to, leading key medical writing projects and activities across therapeutic areas and preparing (under minimal supervision) scientific and regulatory documents related to the clinical development of investigational and marketed drugs and biologics. These types of scientific and regulatory documents can include clinical study reports (CSRs), subject narratives, clinical investigator brochures, protocols, briefing documents, and sections of Investigational New Drug Applications (INDs) and New Drug Applications (NDAs)/Biologics License Applications (BLAs) (i.e., integrated summaries of safety and efficacy, product labeling, and summaries and overviews of nonclinical and clinical information).

Primary Responsibilities:

• Acts as medical writing point person for production of preclinical summaries, clinical summaries, pharmacokinetic reports, safety summaries, literature reviews, and other documents needed for regulatory submissions.

• Participates in and contributes to the development of the submission communication strategy for a product.

• Interprets and summarizes data from biostatistical summary tables and listings accurately, precisely, and concisely into narrative text.

• Liaises with internal groups, i.e., Biostatistics, Data Management, Regulatory Affairs, Medical Affairs, Clinical Development, Clinical Operations and R&D Management to obtain necessary information and to ensure the timely implementation of activities related to the production of reports.

• Interacts with and oversees, coordinates and reviews the work of other medical writers, including freelance/contract medical writers and agencies, with support from Director Medical Writing.

Preferred experience includes:

• 3+ years’ in medical writing for the pharmaceutical industry, with a focus on regulatory document preparation; knowledge of drug development process and regulatory guidelines.

• Specific experience working with CNS/Neuroscience compounds.

• Ability to manage projects independently and lead/organize/participate in cross-functional teams.

• Journalism/press publications.

Must possess:

• Strong writing skills and the ability to convert scientific data into a clear, scientifically sound, well-structured ‘story’.

• Ability to self-edit and improve own work to ensure readability, accuracy, consistency and aesthetic presentation of data and information.

• Knowledge of clinical trial and drug development processes.

• Knowledge of and/or ability to quickly assimilate US, ICH and international regulations, requirements and guidance associated with scientific and clinical/regulatory document preparation and submissions.

• Knowledge of Common Technical Document content templates as well as content expectations for IND/NDA/MAA and other regulatory documentation.

• Working knowledge of current electronic document management systems and publishing systems.

• Ability to assimilate, interpret and translate information/data for appropriate audiences.

• Excellent working knowledge of software programs in Windows environment with high proficiency in word processing, flow diagrams, and spreadsheets.

• Ability to learn fast, grasp the 'essence' of a story quickly to convert relevant scientific data/information into high quality summaries and reports.

Education:

A PhD in a life science/Pharm D preferred with 5 or more years of relevant experience; MS with 7 or more years of relevant experience.

Skills: American Medical Writing Association (AMWA) certification or other is desirable, with a specialty in Pharmaceutical Writing.

Job Tags

Similar Jobs