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Relay Therapeutics

Medical Director/Senior Medical Director, Patient Safety & Risk Management

Relay Therapeutics is hiring a Medical Director/Senior Medical Director, Patient Safety & Risk Management in Cambridge, United States. It pays $201k-$351k a year and Level rates it ; you can apply on Relay Therapeutics.

Level's read on this job

  • Level rates this role Little AI ●○○○: aI is not part of the work.
  • The posting mentions safety surveillance, risk management and clinical development among its tools and skills.
  • Level classes it as a senior role.
  • Relay Therapeutics has 11 other open roles on Level.

AI in this role

Lead global medical safety surveillance, signal detection, and risk management for therapeutic products.

safety-surveillancerisk-managementclinical-developmentregulatory-compliancemedical-safety

The Opportunity:

The Medical Director, Patient Safety & Risk Management at Relay Therapeutics will serve as the Global Medical Safety Lead (GSL) and provides strategic and medical leadership for the safety surveillance and risk management of Relay Therapeutic assigned products throughout the product lifecycle. This role is responsible for the evaluation, interpretation, and communication of safety information; signal detection and management; benefit-risk assessment; and development of risk minimization strategies to ensure patient safety and regulatory compliance. In addition, the GSL will support the medical review of individual case safety reports and safety surveillance activities as needed for assigned Relay Therapeutic products. The GSL will lead the cross functional Safety Management Team in the evaluation of safety signals and implementation of risk minimization activities for Relay Therapeutic products.

We are seeking a safety physician, who thrives in a dynamic, agile biotech environment. Reporting to the Executive Director, Patient Safety & Risk Management, this individual serve as a key collaborator and leader in cross functional clinical program teams, including Clinical Development, Clinical Operations, Biostats, Data Management and Regulatory Affairs. The successful candidate will play a critical role in advancing the development of transformative therapies by providing medical safety expertise.

Your Role:

  • Direct the planning, preparation, writing and review of safety aggregate reports, including DSUR.
  • Train/collaborate and support qualified PSRM staff on medical review, safety surveillance activities and authoring of aggregate reports.
  • Provide benefit-risk assessment on potential safety signal or in safety documents/reports and leads product benefit-risk assessment discussions at safety management meetings.
  • Lead cross functional safety management team meetings and escalate safety issues including preparing and presenting of safety issue and recommendation to the executive decision-making body.
  • Contribute to the development of Investigator Brochures, Protocols, Subject Informed Consent, statistical analysis plans, integrated safety summary, RMP/REMS, and other study related documents
  • Support and collaborate with cross functional teams on safety related activities including providing responses to safety related queries from regulatory authorities and IRB/EC.
  • Ensure compliance with regulatory guidelines and internal processes and procedures, to be inspection ready and serve as SME in audits and inspections.
  • Serve as back-up medical review/sponsor approval of ICSRs and ensure appropriate medical evaluation of individual case safety reports and emerging safety trends.

Your Background:

  • MD, DO or medical degree from an accredited medical school and completion of an accredited medical or surgical residency or clinical experience in either academic setting or private practice
  • A minimum of drug safety experience 7-10 years in the pharmaceutical industry
  • Experience leading cross functional teams and/or projects
  • Expertise in analyzing and presenting complex medical-scientific data from broad range of sources required
  • Experience providing medical leadership and strategic review of aggregate safety reports (DSUR, PBRER/PSUR) is required
  • Knowledge of global risk management planning including RMPs, REMS (Risk Evaluation and Mitigation strategies) and risk minimization strategies required
  • Expertise in global regulations governing safety surveillance and risk management
  • Prior NDA filing (ISS drafting and review) experience strongly preferred

Estimated Salary Range: [$201,000 - $351,000].

The range provided above is based on what we believe to be a reasonable estimate for this job at the time of posting. Actual base salary will depend on a number of factors, including but not limited to, a candidate’s education, experience, skills and location.

#BP1

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!

How we rate this

Medical Director/Senior Medical Director, Patient Safety & Risk Management at Relay Therapeutics rates 0 out of 100 for how much of the daily work is AI. That makes it Little AI (AI Level 1 of 4). The level is about AI in the job, not seniority.

Classification

Little AI. AI is not part of the work.

  1. ●●●● Builds AI80 to 100
  2. ●●●○ Works on AI60 to 79
  3. ●●○○ Uses AI40 to 59
  4. ●○○○ Little AI0 to 39

Levels come from how often the tools, models and workflows of the role are named in the posting itself. Read the description and count the AI tools, models and workflows it names.

Prepare for this job

Built from this posting and from similar jobs on Level.

Skills and AI tools this role asks for

Safety SurveillanceRisk ManagementClinical DevelopmentRegulatory ComplianceMedical Safety

Questions you could be asked

  1. Tell me about a project where safety surveillance was part of your work. What did you do?
  2. Tell me about a project where risk management was part of your work. What did you do?
  3. Tell me about a project where clinical development was part of your work. What did you do?
  4. Tell me about a project where regulatory compliance was part of your work. What did you do?
  5. Tell me about a project where medical safety was part of your work. What did you do?

Adapt your resume

  • List these exact terms on your resume: Safety Surveillance, Risk Management, Clinical Development, Regulatory Compliance, and Medical Safety. An applicant tracking system matches the wording, not the idea.
  • Attach one line of real, concrete experience to at least one of them. A tool named with nothing behind it rarely survives a human read.

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