Medical Director, Clinical Research, Endocrinology

Crinetics Pharmaceuticals

Medical Director overseeing clinical research in endocrinology at Crinetics Pharmaceuticals. Supporting development and execution of clinical trials within a multidisciplinary team.

Posted 7/16/2026full-timeRemote • California • 🇺🇸 United StatesLead💰 $270,000 - $298,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical research and development, with a strong focus on endocrinology, regulatory compliance, and medical monitoring. Proven ability to lead clinical trials, collaborate with cross-functional teams, and provide scientific oversight while ensuring adherence to GCP and regulatory standards.

Highest-signal resume keywords

MD DegreeClinical Research ExperienceEndocrinology Board CertificationGood Clinical Practice (GCP)FDA and EMA Regulations

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial DesignMedical MonitoringClinical Protocol DevelopmentData AnalysisRegulatory Document PreparationPatient Reported OutcomesBiostatisticsClinical PharmacologySafety Parameter ReviewSubmission Activities

Soft Skills

Leadership SkillsInterpersonal SkillsCollaborationStrategic ThinkingPresentation Skills

Certifications & Qualifications

Endocrinology Board Certification

Industry Keywords

Clinical Development Plan (CCDP)ICH GuidelinesClinical OperationsRegulatory Agency InteractionsClinical Research

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Support the development and execution of Crinetics' endocrinology portfolio as part of a multidisciplinary development team
Contribute to the concise clinical development plan (CCDP)
Support the design and conduct of clinical trials across assigned therapeutic areas
Provide medical and scientific input to publications
Support Medical Affairs
Help represent Crinetics to academic, regulatory, and patient organizations
Partner with the cross-functional team to shape a concise Clinical Development Plan (CCDP) for the indication of interest, building consensus toward Executive Team approval and maintaining the plan over time
Lead the design, planning and implementation of clinical trials consistent with this CCDP
Provide scientific and clinical direction for the development of clinical protocols (and, in early stages, clinical trial outlines [CTOs] and synopses), amendments, and related documents (e.g., informed consent)
Work with Medical Writing to ensure content accuracy and medical integrity
Provide medical monitoring for clinical studies in collaboration with CRO medical monitors
Ensure that clinical trials are conducted according to GCP and all applicable regulatory requirements
Provide clinical and scientific input to HEOR-led Patient Reported Outcome research across the studies
Provide medical and scientific oversight needed to support enrollment feasibility and protocol-driven eligibility
Participate in ongoing and formal data analyses and review for CSR completion and planned/actual filing activities
Contribute to the development of clinical sections of regulatory documents such as Investigators' Brochures, briefing books, safety updates, IND/BLA submission documents, responses to Health Authorities questions
Lead trial-related advisory boards, investigator meetings, protocol training meetings
Collaborate with Medical Affairs and Commercial members to develop effective working relationships with key investigators, key opinion leaders and patient advocates to optimize scientific quality/innovation of clinical study design, execution, reporting and publication
Provide medical/clinical expertise to publications planning and drafting
Provide oversight of clinical programs across planning, execution, and completion of clinical trials, ensuring compliance with all applicable regulations and guidance, ICH/GCP, and Crinetics SOPs, in partnership with Clinical Operations
Attend conferences and remain current with relevant therapeutic area information
Serve as the external clinical "face" of Crinetics in interactions with development partners, and leading clinical discussions at advisory boards, as needed.

Requirements

What you’ll need

MD degree with at least 5+ years clinical research experience within industry or academia
Endocrinology subspecialty board certification preferred
Thorough knowledge of clinical medicine, clinical pharmacology and associated disciplines (e.g., biostatistics, data management, medical writing)
Deep understanding of strategic and operational aspects of clinical research and product development
Solid understanding of FDA and EMA regulations and expectations, Good Clinical Practice, ICH guidelines, and clinical drug development
Familiarity with regulatory agency interactions (FDA and/or EU), whether through direct participation or supporting submission activities
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, including the composition of SAE narratives)
Excellent leadership skills and ability to function effectively in a fast-paced, high accountability environment
Superior interpersonal skills focusing on collaboration and influencing capabilities supported by great presentation skills
Strategic thinker, team leader and individual contributor capable of working in a high growth, dynamic, science-driven environment
Ability to conceive and execute innovative approaches to clinical development while taking into account the safety and the comfort of the patient
Can also take the role of a self-starter individual contributor, 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 and remaining flexible
Collaborative, effective leadership skills, with the ability to build and maintain strong interpersonal relationships, gaining trust and confidence from all levels within and external to the organization
Ability to inspire and earn respect of the leadership team, Board members, the regulatory authorities, the investment community, colleagues, and staff
Respectful of the ideas and experience of all members of the Crinetics team
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.

Benefits

Comp & perks

Health insurance plans for employees (and their families) to include medical, dental, vision and basic life insurance
20 days of PTO
10 paid holidays
Winter company shutdown
Discretionary annual target bonus
Stock options
401k match