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Gilead Sciences, Inc.
Director, Clinical Development (MD)
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What they do
A Clinical Director directs and manages a medical practice, clinic, hospital, or other clinical setting. Organizes and manages of staff physicians, policy implementation, and ensures that standards for medical care are communicated and maintained.
$166,864 / year median in California
+16% projected growth
Job Description
Onsite Required United States
- California
- Foster City United States
- California
- Thousand Oaks United States
- California
- El Segundo United States
- New Jersey
- Parsippany United States
- Maryland
- Frederick Full time
R0054522
We're here for one reason and one reason only- to cure cancer.
- Job Description
- The Medical Director will lead the execution of multiple clinical trials in hematologic malignancies, partnering closely with internal and external stakeholders to advance a novel CAR T-cell therapy for patients.
- Responsibilities include, but are not limited to:
- + Provide medical monitoring to multiple oncology clinical trials + Lead project teams to design and implement clinical studies + Write protocols, investigator brochures, clinical study reports and review clinical trial documents + Conduct investigator meetings and lead site initiation visits with clinical trial investigators + Execute and deploy drug development strategic plans, develop contingency plans, provide technical and strategic advice, and meet milestones and budgets + Translate findings from research and nonclinical studies into clinical development opportunities + Interact with clinical investigators and thought leaders + Work with internal regulatory affairs team and other ethical guidelines relevant to the pharmaceutical industry, and ensure compliance with these external guidelines + Work with internal pre-clinical scientists, translational scientists, business and commercial organizations in a cross functional manner + Work in a team environment comprising clinical operations, biomarker specialists, CROs, and regulatory affairs + Perform other duties as required + Support, provide input into regulatory filing documents, conduct regulatory filings •
Basic Qualifications:
- + MD or equivalent with 4+ years of experience managing oncology trials
Preferred Qualifications:
- + Board certification/specialization in Hematology or Oncology + At least 2 years of relevant drug development experience, either within industry or as a clinical investigator/physician scientist in academia, or equivalent experience + Proven clinical development strategist with experience designing, implementing and conducting clinical trials, with emphasis on proof-of-concept and first-in-human studies + Knowledge of carrying out hematology/oncology clinical trials, including knowledge of hematology/oncology treatment options + Strategic leadership and tactical skills, excellent initiative and judgment, and demonstrated ability to positively represent the goals of Kite + Demonstrated ability to develop and maintain excellent working relationships with both internal colleagues and external contacts, including key thought leaders, and investigators + Demonstrated ability to work well in teams in a cross functional manner + Ability to communicate and work independently with scientific/technical personnel + Ability to think critically, and demonstrated troubleshooting and problem solving skills + Self-motivated and willing to accept temporary responsibilities outside of initial job description + Comfortable in a fast-paced small company environment with minimal direction and able to adjust workload based upon changing priorities + May travel up to 30% The salary range for this position is:
Bay Area:
$261,375.00- $338,250.
Other US Locations:
$237,575.00- $307,450.
- . For additional benefits information, visit: https://www.gilead.com/careers/compensation-benefits-and-wellbeing
- Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.
- For jobs in the
United States:
- Kite Pharma is committed to providing equal employment opportunities to all employees and applicants for employment, and is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds, and experiences.
NOTICE:
EMPLOYEE POLYGRAPH PROTECTION ACT
(http://www.dol.gov/whd/regs/compliance/posters/eppac.pdf)YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT
Kite Pharma will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, (c) consistent with the legal duty to furnish information; or (d) otherwise protected by law. Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team. Kite Pharma provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion.For Current Kite Pharma Employees and Contractors:
- Please apply via the Internal Career Opportunities portal in Workday.
- Change The World With Us
- Everyone at Kite is grounded by one common goal
- curing cancer.