Medical Director, Endocrinology

Biopharma Careers; Boston (MA); Hybrid; USD 240,000 - 360,000; Full time

Job summary

Vertex is seeking a Clinical Development Medical Director in Boston to serve as the Medical Lead for multiple clinical trials across phases, guiding study strategy and safety monitoring with cross-functional teams.

The role requires MD/DO or equivalent, board certification, and roughly 10 years in clinical research, with strong knowledge of GCP, biostatistics, and regulatory submissions. Hybrid-eligible, on-site presence in Boston, with total rewards package.

Qualifications

• MD, DO or equivalent ex-US medical degree is required.
• Board certification/eligibility in a medical, pediatric or surgical specialty is highly desirable.
• Typically requires 10 years of basic or clinical research experience in academic or industrial settings.

Responsibilities

• Leads the development of Study Protocols, Investigator Brochures, Clinical Development Plans and other key study documents with minimal guidance.
• Serves on cross-functional Study Execution Teams (SET) for assigned trials to achieve efficient, high-quality study execution.
• Participates in regulatory documents for regulatory submissions (INDs, CTAs, safety reports, annual reports).
• Provides scientific input to study documents and analysis plans, and acts as liaison between Translational Medicine/Clinical Development and Regulatory Affairs/Clinical Operations.
• Represents Vertex to outside medical personnel in protocol development and study conduct.
• Performs other duties related to clinical programs.

Skills

Clinical trial strategy

Study protocol development

Medical monitoring

Cross-functional leadership

Regulatory submissions

Biostatistics knowledge

GCP knowledge

Excellent communication

Education

MD, DO or equivalent ex-US medical degree

Board certification/eligibility in a specialty

Typically requires 10 years of basic or clinical research experience

Job description

Job Description

Vertex completed its acquisition of Crinetics Pharmaceuticals on September 1, adding commercial and pipeline endocrinology programs to Vertex’s innovation portfolio. The acquisition is expected to accelerate revenue growth and enhance the Company’s long-term earnings profile.

The acquired portfolio includes PALSONIFY® (paltusotine), atumelnant, and several additional pipeline programs. PALSONIFY is the first and only once-daily oral therapy for acromegaly; it has launched in the United States, is approved in the European Union, and is under review by other global regulatory authorities.

Atumelnant is an investigational, once-daily oral adrenocorticotropic hormone (ACTH) receptor antagonist in Phase 3 development for congenital adrenal hyperplasia (CAH) and Phase 2 development for Cushing’s syndrome. We are seeking a pediatric or adult endocrinologist to contribute clinical expertise to the development of atumelnant.

The Clinical Development Medical Director will serve as the Medical Lead for Vertex clinical trials, working with cross-functional multidisciplinary study teams on clinical trial strategy, design and execution and serving as the Medical Monitor responsible for monitoring the safety of enrolled subjects on assigned trials.The incumbent will work on multiple trials inall Phases of clinical development,and may also participate in other selected projects in clinical development.

Key Duties and Responsibilities

Leads the development of Study Protocols, Investigator Brochures, Clinical Development Plans and other key study 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 sections of INDs and CTAs, 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 (ICF), clinical research forms (CRF), statistical analysis plans (SAP), clinical pharmacology analysis plans (CPAP), and clinical study reports (CSR). Acts as liaison between Translational Medicine/Clinical Development and other internal groups at Vertex (e.g., Regulatory Affairs, Clinical Operations) for assigned studies

Represents Vertex to outside medical personal in the development of clinical protocols and study conduct

Performs other duties as assigned related to clinical programs

Knowledge and Skills

Excellent oral and written communication skills

Ability to work collaboratively in a fast‑paced, team‑based, matrix environment and to function independently as appropriate

Effective at building alliances across functions, based on end‑to‑end drug development thinking and experience

Board certification/eligibility in a medical, pediatric or surgical subspecialty

Education and Experience

MD, DO or equivalent ex‑US medical degree

Board certification/eligibility in a specialty field is highly desired

Typically requires 10 years of basic or clinical research experience in an academic or industrial setting, or the equivalent combination of education and experience

Typically requires experience in analysis of research data and publications; working knowledge of biostatistics; working knowledge of GCP, scientific and clinical research methods and clinical study design

Typically requires experience with design, execution, and analysis of clinical trials required

About Vertex

Vertex is a global biotechnology company that invests in scientific innovation to create transformative medicines for people with serious diseases and conditions. The company has approved therapies for cystic fibrosis, sickle cell disease, transfusion‑dependent beta thalassemia, acute pain and acromegaly, and it continues to advance clinical and research programs in these areas. Vertex also has a robust clinical pipeline of investigational therapies across a range of modalities in other serious diseases where it has deep insight into causal human biology, including IgA nephropathy, neuropathic pain, APOL1‑mediated kidney disease, primary membranous nephropathy, congenital adrenal hyperplasia, ACTH‑dependent Cushing's syndrome, autosomal dominant polycystic kidney disease, type 1 diabetes, generalized myasthenia gravis, and myotonic dystrophy type 1.

Vertex was founded in 1989 and has its global headquarters in Boston, with international headquarters in London. Additionally, the company has research and development sites and commercial offices in North America, Europe, Australia, Latin America and the Middle East. Vertex is consistently recognized as one of the industry's top places to work, including 16 consecutive years on Science magazine's Top Employers list and one of Fortune’s 100 Best Companies to Work For. For company updates and to learn more about Vertex's history of innovation, visit www.vrtx.com or follow us on LinkedIn , Facebook , Instagram , YouTube and X .

At Vertex, we embrace continuous learning and encourage employees to stay informed on advances in AI, technology, automation, and industry trends. We seek talent who bring an external perspective, demonstrate curiosity and sound judgment, and thoughtfully adopt new capabilities that improve decision‑making, drive innovation, increase efficiency, and help deliver better outcomes for patients.

Pay Range

$240,000 - $360,000

Disclosure Statement

The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, experience, and other job‑related factors permitted by law.

At Vertex, our Total Rewards offerings also include inclusive market‑leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations. From medical, dental and vision benefits to generous paid time off (including a week‑long company shutdown in the Summer and the Winter), educational assistance programs including student loan repayment, a generous commuting subsidy, matching charitable donations, 401(k) and so much more.

Flex Designation:

Hybrid‑Eligible Or On‑Site Eligible

Flex Eligibility Status:

In this Hybrid-Eligible role, you can choose to be designated as:

1. Hybrid: work remotely up to two days per week; or select

2. On‑Site: work five days per week on‑site with ad hoc flexibility.

Note: The Flex status for this position is subject to Vertex’s Policy on Flex @ Vertex Program and may be changed at any time.

Company Information

Vertex is a global biotechnology company that invests in scientific innovation.

Vertex is committed to equal employment opportunity and non‑discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at [e-mail]