Job Overview:
Senior Medical Writer
Remote: US or Canada
Medical Writers in the Late Phase group is responsible for preparation and coordination of clinical study protocols and clinical study reports (CSRs), and other documents as needed. Provide support for and participate in development of submission level documents under guidance of senior staff. Production of scientific publications and other documents (e.g., abstracts, posters, manuscripts, etc.). Interpretation of clinical, pharmacokinetic, pharmacodynamic and statistical results as appropriate. Oversees and coordinates activities of other writers on higher complexity narrative projects. Ensure timely delivery of high quality documents to internal customers and Sponsors. Provision and development of intra- and inter-departmental training. Works with the management team to provide guidance and mentoring to Medical Writers to ensure best working practices are maintained. Scientific presentations both internally within Labcorp Drug Development and externally (e.g., conferences). Represents the company at scientific meetings and meetings with clients. Foster excellent working relationships with all clients, both internal and external, with the highest quality of service in a cost-effective manner on time, every time.
Minimum of first degree in life sciences (or equivalent); advanced degree (e.g., PhD or Masters) preferred
Experience:Labcorp Drug Development
Durham North Carolina
United States
Healthcare - Allied Health
(No Timezone Provided)
Job Overview:
Senior Medical Writer
Remote: US or Canada
Medical Writers in the Late Phase group is responsible for preparation and coordination of clinical study protocols and clinical study reports (CSRs), and other documents as needed. Provide support for and participate in development of submission level documents under guidance of senior staff. Production of scientific publications and other documents (e.g., abstracts, posters, manuscripts, etc.). Interpretation of clinical, pharmacokinetic, pharmacodynamic and statistical results as appropriate. Oversees and coordinates activities of other writers on higher complexity narrative projects. Ensure timely delivery of high quality documents to internal customers and Sponsors. Provision and development of intra- and inter-departmental training. Works with the management team to provide guidance and mentoring to Medical Writers to ensure best working practices are maintained. Scientific presentations both internally within Labcorp Drug Development and externally (e.g., conferences). Represents the company at scientific meetings and meetings with clients. Foster excellent working relationships with all clients, both internal and external, with the highest quality of service in a cost-effective manner on time, every time.
Minimum of first degree in life sciences (or equivalent); advanced degree (e.g., PhD or Masters) preferred
Experience: