Vertex

Biotechnology

ClinicalDevelopmentAssociateMedicalDirector-Pain

$204–306k Boston, Massachusetts, United States FULL TIME Remote Friendly
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Director candidates.

The Brief

“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.

Biotechnology

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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