Medical Director

Relay Therapeutics; Cambridge (MA); Remote; USD 200,000 - 300,000; Full time

Job summary

A precision medicine company is seeking a Medical Director in Cambridge, MA to drive clinical strategy and trial execution. The role involves collaborating with senior medical staff and leading clinical development for oncology products. Ideal candidates will have an MD or MD/PhD, significant clinical development experience, and a strong background in solid tumors. Remote work is an option.

Qualifications

• 5+ years of clinical development experience in academic or industry settings.
• Experience working with solid tumors, especially breast oncology preferred.
• Exposure to the design and execution of clinical trials.

Responsibilities

• Collaborate with and lead clinical strategy, trial design, and execution.
• Provide expert medical review and assessment of clinical data.
• Manage drug safety and pharmacovigilance activities.

Skills

Effective communication

Collaboration

Clinical development experience

Expert medical review

Education

MD, MD/PhD or other advanced degree

Job description

Overview

As a Medical Director at Relay Tx, you will help advance our clinical pipeline from IND to proof of concept to registration. Specifically, you will collaborate with senior medical staff to drive clinical strategy, clinical trial design, and execution. Working cross-functionally with clinical project management, regulatory affairs, clinical operations, biostatistics, data management and medical writing, you will play a key role as Relay Tx continues to introduce product candidates into the clinic. You will provide clinical leadership to R&D teams and will work closely with Development leadership.

About You:

• Collaborate with senior medical staff, drug discovery teams, translational oncology, clinical operations, clinical investigators and disease-specific experts to design and execute early clinical development plans that definitively test key translational hypotheses for Relay Tx medicines and establish clinical proof-of-concept as soon as possible after entering human testing.
• Write clinical sections of key documents, including Investigator’s Brochures, IND summary documents, CTAs for initiation of ex-US studies and work with senior medical staff for responses to questions from regulatory authorities, IRBs, and ethics committees.
• Provide expert medical review, assessment, and interpretation of clinical data and prepare results for presentation to internal clinical development leadership and external stakeholder including regulatory authorities.
• Manage drug safety and pharmacovigilance activities for ongoing trial(s).
• Attend and support clinical site initiation visits.
• Rapidly integrate new insights derived from on-going Relay Tx or external clinical trials, translational science or basic science into Relay Tx development plans and clinical trial activities.
• Collaborate with research leadership and drug discovery teams to shape the Relay Tx drug discovery portfolio.
• Proactively manage communication and build strong collaborative relationships with key stakeholders
• Ensure Relay Tx maintains the highest standards of compliance and ethical behavior in the design, conduct, interpretation and communication of clinical trials, clinical trial data, and clinical trial results.

Your Background:

• A dynamic team player and effective communicator that thrives in a fast-paced environment.
• Experience working with solid tumors, breast oncology preferred.
• MD, MD/PhD or other advanced degree with 5+ years of clinical development experience in academic and/or industry settings with work in . Motivated candidates with lesser experience and a passion to learn precision oncology clinical development and contribute to cross functional development teams will also be considered. .
• Exposure to design and execution of clinical trials; protocol development and design, development of case report forms, and statistical analysis plans.
• Exposure to working closely with investigative sites, including principal investigators, sub-investigators, study coordinators, and other site personnel involved in clinical trials.
• Excellent written and oral communication skills.
• The successful applicant will thrive in the Relay Tx corporate culture where the core values are relentless, fearless, craftsmanship, candor, and humanity. You will be a key contributor to Relay clinical development and enabled to make a significant positive impact for patients.

We are open to remote employees

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About Relay Therapeutics

Relay Therapeutics is a clinical-stage precision medicines company transforming the drug discovery process with the goal of bringing life-changing therapies to patients. Built on unparalleled insights into protein motion and how this dynamic behavior relates to protein function, we aim to effectively drug protein targets that have previously been intractable, with an initial focus on enhancing small molecule therapeutic discovery in targeted oncology. Our Dynamo platform integrates an array of leading-edge experimental and computational approaches to provide a differentiated understanding of protein structure and motion to drug these targets. We have built a world-class team of leading experts from each of these disciplines, and they are driven by a deep collaboration at every step of our drug discovery process.

Our team is equal parts fearless and relentless, with a shared passion for working collaboratively in intellectually stimulating environments. If you’re excited by the challenge of putting protein motion at the heart of drug discovery and passionate about making a difference in the lives of patients, join us!

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