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Senior Director, Clinical Pharmacology - Foster City, United States - Workday
Description
For Current Gilead Employees and Contractors:Please log onto your
Internal Career Site
to apply for this job.
At Gilead we believe every employee deserves a great leader.
As a people leader now or in the future, we expect that you will model and create an environment of inclusion, be intentionally focused on the hiring, development, growth and retention of talent, and empower teams to align and achieve goals.
Job DescriptionAs a Senior Director within the Clinical Pharmacology Group at Gilead, you will have significant responsibility and accountability for clinical pharmacology programs in
Inflammation/ Oncology
. As a member of the Clinical Pharmacology team you will have unparalleled opportunity to be involved with every aspect of the product development process, from first-in human through approval, including post-marketing activities. In this role, you will have the advantage of providing input into a breadth of products within and across your area of responsibility. We seek to provide a fun and rewarding career and a continuous learning experience.
Your tasks and responsibilities will include:
Leading clinical pharmacology studies of the highest complexity
Providing strategic leadership and demonstrating accountability for the clinical pharmacology programs supporting Phase 1-4 clinical development for development compounds in your therapeutic area
Developing and implementing new clinical pharmacology tools and technologies to drive smarter drug development for programs.
Representing the department and providing subject matter expertise on cross-functional project teams
Developing and maintaining collaborative working relationship with colleagues within and outside the department
Supervising, developing and mentoring junior level scientists, both direct reports and via matrix structure in clinical pharmacology teams
Authoring/reviewing/approving
clinical protocols, analysis plans, study reports and regulatory submissions
Developing high quality clinical pharmacology plans and content for global regulatory submissions, including INDs, IBs, NDAs, MAAs and pediatric plans
Maintaining and establishing relationships and agreements with contract vendors
Evaluating departmental and broader organizational SOPs as fit for purpose, in compliance with current scientific standards and regulatory requirements
Ensuring adherence to agreed timelines and budgets to insure prompt and accurate execution of deliverables from clinical pharmacology studies and programs
Understanding the impact of decisions and actions on the business and consulting with colleagues and management as applicable
Participating in and collaborating with individuals from across the business in special projects
Developing and presenting training within and outside the department
Specific education, experience and skills required for this role:
At least 12 years' experience and a, PhD, PharmD or MD degree with emphasis in clinical pharmacology, pharmacokinetics or a related scientific discipline
In-depth knowledge of pharmacokinetic and other analysis software programs (e.g. WinNonlin, GraphPad, etc.)
Thorough knowledge of current and emerging scientific standards regulatory requirements for assigned territories
Excellent written and oral communication skills and ability to convey complex technical information clearly
Confidence and ability to present to and influence senior leaders
Ability to critically analyze problems and provide creative solutions
Confidence and discipline to work autonomously
Genuine curiosity and drive to ask questions – looking for the 'why' of every project
Desire to strive for continuous improvement
The salary range for this position is: $248, $321, Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location.
This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package.
Benefits include company-sponsored medical, dental, vision, and life insurance plans*.For additional benefits information, visit:
United States:
As an equal opportunity employer, Gilead Sciences Inc. is committed to a diverse workforce. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, age, sexual orientation, physical or
mental
disability, genetic
information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws.
for assistance.
For more information about equal employment opportunity protections, please view the
'Know Your Rights'
poster.
NOTICE:
EMPLOYEE POLYGRAPH PROTECTION ACT
YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT
PAY TRANSPARENCY NONDISCRIMINATION PROVISION
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.
Gilead provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion.
For Current Gilead Employees and Contractors:
Please log onto your
Internal Career Site
to apply for this job.
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