Vertex
Biotechnology
ClinicalDevelopmentAssociateMedicalDirector-Pain
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“Clinical Development Associate Medical Director- Pain at Vertex. Skills: Clinical development, Medical monitoring, Regulatory submissions. Serve as Medical Lead for clinical trials. Work with cross-functional teams on trial strategy”
Industry & Context.
What They're Looking For.
Must Have
MD, DO or equivalent ex-US medical degree, 8 years of basic or clinical research experience
Nice to Have
Global clinical research experience, Experience interacting with regulatory authorities, Board certification/eligibility in a relevant medical specialty, Clinical training in a relevant medical specialty
What You'll Do.
Serve as Medical Lead for clinical trials
Work with cross-functional teams on trial strategy
Design clinical trials
Execute clinical trials
Report on clinical trials
Monitor safety of enrolled subjects
Ensure scientific integrity of studies
Participate in other projects
Develop Study Protocols
Develop Investigator's Brochures
Develop Clinical Development Plans
Serve on cross-functional Study Execution Teams
high-quality study execution
Prepare regulatory documents
Support regulatory submissions
Prepare clinical section of INDs
Prepare IND safety reports
Prepare annual reports
Respond to regulatory authorities
Respond to Ethics Committees/IRBs
Provide scientific input to study documents
Provide clinical input to study documents
Provide input to analysis plans
Provide input to informed consent forms
Provide input to clinical research forms
Provide input to statistical analysis plans
Provide input to clinical pharmacology analysis plans
Provide input to clinical study reports
Act as liaison between Clinical Development and internal
Represent Vertex to outside medical personnel
Develop clinical protocols
Conduct study conduct
Report study results externally
Perform other duties as assigned
How You'll Work.
Team & Collaboration
Cross-functional teams; Study Execution Teams; Internal groups at Vertex
Communication Scope
Oral communication; Written communication
Full Job Description
**Job Description** **General Summary:** The Clinical Development Associate Medical Director will serve as the Medical Lead for clinical trials, working with cross-functional teams on trial strategy, design, execution, and reporting. In addition to oversight and accountability for the study as a whole, this role will serve as the internal primary Medical Monitor accountable for monitoring the safety of enrolled subjects and ensuring scientific integrity. The incumbent may participate in other projects to support the clinical development program. **Key Duties and Responsibilities:** * Participates in the development of Study Protocols, Investigator's Brochures, Clinical Development Plans and other key documents in conjunction with other line functions and with minimal guidance * Serves on cross-functional Study Execution Teams (SET) for assigned trials, working with other team members to achieve efficient, high-quality study execution * Participates in the preparation of regulatory documents in support of regulatory submissions, including clinical section of INDs and CTAs, IND safety reports and annual reports for assigned trials, responses to regulatory authorities and Ethics Committees/IRBs, and other documents as appropriate * Provides scientific and clinical input to study-related documents and analysis plans including informed consent forms, clinical research forms, statistical analysis plans, clinical pharmacology analysis plans, and clinical study reports * Acts as liaison between Clinical Development and other internal groups at Vertex (e.g., Regulatory Affairs, Clinical Development Execution) for assigned studies * Represents Vertex to outside medical personnel in the development of clinical protocols, in study conduct, and in external reporting of study results * Performs other duties as assigned related to other aspects of Clinical Development **Knowledge and Skills:** * Strong oral and written communication skills * Ability to work collaboratively in a fa
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