Vice President, Clinical Research – Endocrinology

🕒 March 9

🏄 California – Remote

🏄 California – Remote

💵 $346k - $433k / year

⏰ Full Time

🔴 Lead

🧪 Clinical Research

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

Crinetics Pharmaceuticals

WebsiteLinkedInAll Job Openings

201 - 500 employees

Founded 2015

🧬 Biotechnology

💊 Pharmaceuticals

⚕️ Healthcare Insurance

Biotechnology • Pharmaceuticals • Healthcare Insurance

Crinetics Pharmaceuticals is a biotechnology company that develops innovative therapies for endocrine diseases. The company is focused on addressing unmet medical needs by creating treatments for conditions such as acromegaly, carcinoid syndrome, ACTH-dependent Cushing’s syndrome, congenital adrenal hyperplasia, and other endocrine disorders. Crinetics is committed to improving the quality of life for patients through cutting-edge science and robust clinical trials. Their pipeline includes promising candidates like paltusotine, which has been accepted by the U. S. Food and Drug Administration for the treatment of adult patients with acromegaly. The company collaborates with healthcare practitioners and stakeholders to ensure that their therapies address real-life problems effectively and build value for investors by entering market niches with significant needs.

📋 Description

• serve as deputy for CMO on as need basis • play a key role in the design and implementation of the clinical development strategy across the entire endocrinology portfolio • lead creation and implementation of innovative trial designs to accelerate delivery of high-quality data • provide clinical leadership and lead communication to upper management on trial issues • author and/or review clinical documents required for clinical studies • contribute to/lead clinical strategies for successful development of Crinetics endocrine-related drug candidates • serve as the Clinical Research expert to conceive and refine Target Product Profiles (TPP) • oversee or lead the creation and implementation of a Clinical Development Plan (CDP) for each indication • serve as clinical subject matter expert in discussions with external experts and regulatory authorities • engage with Discovery team provide input on selection of future targets • develop strong external relationships with investigators, research sites, patient advocacy groups and KOLs

🎯 Requirements

• MD degree • at least 13 years clinical research experience within a biopharmaceutical company • minimum of 12 years in a supervisory/leadership role • Board certification in internal medicine or related specialty • specialty training in adult or pediatric endocrinology preferred • broad understanding and practice of endocrinology • hands-on experience working in clinical pharmacology/translational medicine/early development capacity is required • experience in interacting with the FDA and/or EU regulatory agencies • previous successful regulatory authorization experience strongly preferred • demonstrated expertise and experience in translational medicine • strong general knowledge of GCP, ICH guidelines and regulatory requirements that apply to clinical drug development • intimate knowledge of medical monitoring of clinical trials • excellent leadership skills • strong project planning, negotiation, and presentation skills

🏖️ Benefits

• discretionary annual target bonus • stock options • ESPP • 401k match • 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 • winter company shutdown