Senior Medical Director

Crinetics Pharmaceuticals • Headquarters, KY

4d • $330,000 - $362,000

About The Position

Crinetics is a pharmaceutical company based in San Diego, California, developing much-needed therapies for people with endocrine diseases and endocrine-related tumors. We were founded by a dedicated team of scientists with the simple belief that better therapies developed from rigorous innovation can lead to better lives. Our work continues to make a real difference in the lives of patients. We have a prolific discovery engine and a robust preclinical and clinical development pipeline. We are driven by science with a patient-centric and team-oriented culture. Crinetics is known for its inclusive workplace culture. We are also a dog-friendly workplace. This is an exciting time to join Crinetics as we shape our organization into the world’s premier fully-integrated endocrine company from discovery to patients. Join our team as we transform the lives of others. Position Summary: The Senior Medical Director, Clinical Research will be working within a multi-disciplinary team and will be accountable for developing the strategy and the Clinical Development Plan for one or more indications for a specific Crinetics' compound. The incumbent will have hands-on responsibility designing, executing, and analyzing clinical trials. The incumbent will have a key role in the understanding and interpretation of the results from these studies as well as the preparation of the summary documents needed for a global submission to regulatory authorities.

Requirements

• MD degree with 10+ years in biopharmaceutical and/or pharma companies with 5+ years of clinical development spanning across Phase I–IV trials
• A minimum of 10 years in a leadership role with 3-5 years of people management experience.
• Experience from clinical practice in internal medicine/endocrinology
• Experience in designing, planning, and executing First-in-Human studies, Phase 2 proof-of concept studies and preferably also global phase 3 trials- with the focus on experience in bridging between discovery/research into the clinic.
• Experience with application of biomarkers.
• Strong general knowledge of GCP, ICH guidelines and regulatory requirements and trial design that apply to clinical drug development.
• Intimate knowledge of and high-level expertise in the day-to-day medical monitoring of clinical trials required (e.g., responding to questions about patient eligibility; review of safety parameters; receiving and processing SAEs, drafting of SAE narratives) including the application of biostatistics, data management, medical writing.
• Excellent leadership skills and ability to function effectively in a fast-paced, high accountability environment.
• Strong project planning, negotiation, and presentation skills as well as an ability to contribute creative yet practical solutions to problems.
• Ability to work independently and collaboratively, prioritizing tasks efficiently and meeting clinical and corporate timelines.
• Strategic thinker, team leader and individual contributor capable of working in a high growth, dynamic, science-driven environment.
• Able to prioritize and parallel process multiple workstreams, comfortable "changing gears" and remaining flexible, as well as making definitive decisions.
• Self-starter, who enjoys rolling up their sleeves and digging into the details; rigorous attention to details and data, while not losing sight of the bigger picture.
• Able to conceive and execute innovative approaches to clinical development.
• Ability to inspire and earn respect of the leadership team, Board members, the investment community, colleagues, and staff.
• Respectful of the ideas and experience of all members of the Crinetics team.
• Well-developed presentation and written communication skills; effective at board level, as well as with the scientific/medical community, advisers, and colleagues.
• Ethical, with highest standards of integrity recognizing that we are the creators of hope for our patients and the health care professionals who serve them as well as stewards of the investments of all our shareholders.

Nice To Haves

• Experience interacting with the FDA and/or EU regulatory agencies is a plus.

Responsibilities

• Clinical leader of one or more endocrinology programs, being integral to developing the clinical strategy and plans.
• Member of global project team(s) and development sub team(s).
• Focus on immediate and short-term (<2 years) strategic planning horizon.
• Contribute as the Clinical Research expert to the conception and regular modifications of the Target Product Profile (TPP).
• Lead the development of the Clinical Development Plan (CDP) for each indication being pursued, using the TPP as a guidance; this includes coordinating cross-functional collaborations with other departments as needed throughout the asset life cycle.
• Conceive and write the Clinical Study Outline for each study in the CDP.
• Lead the discussions and oversee the writing of the study synopsis, study protocol and its amendments. This entails guiding the internal discussions of the successive drafts, providing data analyses to guide medical decisions, consulting with external Medical Experts and Regulatory authorities.
• Review or oversee the review on a regular basis the data input in the EDC for events of interest or needing further investigation and all reports generated from ongoing clinical studies (see next bullet also) and trend analyses.
• Provide senior‑level medical monitoring and safety oversightin cooperation with pharmacovigilance, including review of periodic data listings (e.g. adverse events, protocol deviations, concomitant medications)
• Collaborate with other departments (Biometrics, Clinical Operations, Medical Affairs, a.o.) in all topics related to the conduct and analysis of clinical study results.
• Guide interpretation of clinical data.
• Use the findings and other analyses to contribute to trial-related advisory boards, lead investigator meetings, protocol training meetings.
• Support advisory boards, key opinion leader engagement, and external scientific collaborations
• Contribute to the development of relevant sections of regulatory documents such as amendments to protocols, briefing books, safety updates, responses to Health Authorities questions and collaborate with Regulatory Affairs in the preparation of regulatory interactions.
• Contribute significantly to the preparation, drafting and finalization of all the clinical sections of NDA and MAA.
• Lead the timely drafting of responses to questions from regulatory authorities.
• Provide leadership, career management and personal development to direct reports.
• Other duties as assigned to meet business needs.

Benefits

• In addition to your base pay, our total rewards program consists of a discretionary annual target bonus, stock options, ESPP, and 401k match.
• We also provide top-notch health insurance plans for employees (and their families) to include medical, dental, vision and basic life insurance, 20 days of PTO, 10 paid holidays, and a winter company shutdown.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Education Level: Ph.D. or professional degree