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Scientific Writer

Employer
Bristol Myers Squibb Company
Location
Princeton, NJ, US
Start date
Jan 3, 2019

View more

Discipline
Clinical, Clinical Documentation
Required Education
Bachelors Degree
Position Type
Full time
Hotbed
Pharm Country, Best Places to Work

Job Details

Bristol-Myers Squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases.

One shared journey is moving us forward at Bristol-Myers Squibb. Around the world, we are passionate about making an impact on the lives of patients with serious disease. Empowered to apply our individual talents and ideas so that we can learn and grow together. Driven to make a difference, from innovative research to hands-on community support. Bristol-Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees the resources to pursue their goals, both at work and in their personal lives.

Summary:

Coordinate with DS&B/PCO scientist to generate compliant regulatory documents (study reports, IND summaries, NDA summaries, etc). Act as Coordinating Author to create Cara structures and assign tasks for writing, reviewing and approving documents. Act as Coordinating Author for all Initial IBs

Responsibilities:
  • Coordinate with DS&B/PCO scientist to generate compliant regulatory documents (study reports, IND summaries, NDA summaries, etc).
  • Apply scientific expertise to provide critical assessment of document content to ensure clarity and validity; review (QC) documents for ensure data integrity
  • Work proactively with DS&B/PCO scientists and Dossier Managers to ensure timelines are met
  • Act as Coordinating Author to create Cara structures and assign tasks for writing, reviewing and approving documents
  • Ensure compliance of documents with submission and publication standards
  • Provide leadership in developing processes and associated guidelines relevant to authoring, as well as ensuring that DS&B/PCO scientists receive appropriate training and guidance regarding these
  • Generate and update Model Documents
  • Act as Coordinating Author for all Initial IBs

Qualifications:

1. BS/MS in a relevant scientific discipline, or MS/BS with a minimum of 3 years (MS) to 5 years (BS) in the pharmaceutical industry, preferably within pharmacology/drug metabolism-pharmacokinetics or nonclinical development, with a good understanding of drug discovery, drug development, drug safety, and regulatory document development.

2. Demonstrated strong writing skills as evidenced by authoring and managing the production of nonclinical submission documents.

3. Good understanding of the global pharmaceutical drug development process and requirements for authoring documents for regulatory submissions.

4. Demonstrated ability to analyze and interpret nonclinical and pharmacology data from a broad range of therapeutic areas.

5. Demonstrated ability to manage timelines and quality of work using strong organizational, communication, facilitation, and interpersonal skills in a cross-functional team.

6. Sense of urgency, flexibility, and ability to prioritize or shift priorities to meet aggressive and changing timelines

7. Working knowledge of a document management system and basic knowledge of the document publishing process.

Experiences Desired:

(5-7 pre-hire ideal experiences)

1. Experience writing and managing the production of nonclinical documents; knowledge of regulatory documentation principles and processes.

2. Good knowledge of drug development process (preferably nonclinical development).

3. Understanding of documentation requirements related to regulatory submissions.

4. Worked successfully in a cross-functional project team; ability to facilitate discussions and decision-making with cross-functional team members.

Company

Bristol Myers Squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases.

At Bristol Myers Squibb, we believe in the power of science to address some of the most challenging diseases of our time. Our focus on these unmet needs comes during a remarkable time, when unprecedented scientific breakthroughs are advancing the treatment of disease as never before in human history.

We work every day to transform patients’ lives through science. Each day, our employees around the world work together for patients – they are at the center of everything we do. They inspire us. They are the reason we come to work each day.

We combine the agility of a biotech with the reach and resources of an established pharmaceutical company to create a global leading biopharma company powered by talented individuals who drive scientific innovation.

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Company info
Website
Phone
+1-800-332-2056
Location
430 E. 29th St
14th Floor
New York
New York
10016
United States

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