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Medical Writer

TSR Consulting Services, Inc

This is a Contract position in Chino, CA posted August 14, 2021.

TSR Consulting Services provides best in class staffing solutions to clients nationwide, by staying true to our relentless focus of exceeding the highest professional IT service business standards.

Today, as a NASDAQ company specializing in IT consulting and staff augmentation, TSR continues to expand and transform its services to meet and anticipate its client’s and candidate’s’ needs.

For more than 53 years, TSR’s has been a leader in the industry because of our expertise and knowledge of the job market, our compassion and caring of our clients and consultants and our work environment of respect and inclusion.

Your career is in good hands with TSR because at the end of the day, if YOU THRIVE, WE THRIVE.

Our client, a leading Pharmaceutical company is hiring a Medical Writer on a contracting basis.

Work Location: Princeton NJ Summary: 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, Investigator’s Brochure) ensuring the coordination and integration of the scientific, medical and regulatory input from development team members 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 Participate in relevant filing subteam(s) and ensure effective planning and management of timelines for all components of assigned documents Lead or co-lead (with Doc Lead) teams to define content and data displays for CSR prototypes and shells Able to collaborate with project team to respond to health authority questions, requests, etc.

Provide departmental management with adequate information to help assess resource needs Required skills: PhD/MD/PharmD in a relevant scientific discipline or MS / BS Experience in pharmaceutical regulatory documentation, or equivalent, and good understanding of requirements for regulatory submission documents Demonstrated strong writing skills as evidenced by good quality writing in pharmaceutical regulatory documentation and/or publications in peer-reviewed journals Good understanding of global pharmaceutical drug development and requirements for submission of regulatory dossiers to global health authorities 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)