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Senior Director, Clinical Pharmacology

Scorpion Therapeutics

United States

Remote

USD 228,000 - 342,000

Full time

Today
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Job summary

A leading biotechnology company is seeking a Senior Director for Clinical Pharmacology to lead innovative drug development efforts. The role involves managing Clinical Pharmacology functions, collaborating across departments, and influencing clinical strategies for various therapeutic modalities, including gene editing and therapy.

Benefits

Annual bonus
Annual equity awards
Flexible working options
Generous paid time off
Educational assistance programs
Commuting subsidy
Matching charitable donations

Qualifications

  • 15+ years of relevant post-doctoral employment experience or 20+ years of employment experience with a Master's.
  • Typically requires 5 years of supervisory/management experience.

Responsibilities

  • Defines scientific direction and executes clinical pharmacology plans.
  • Manages a group of Clinical Pharmacologists for Disease Area programs.
  • Directs efforts for small molecule and novel modality programs.

Skills

Clinical pharmacology design
Regulatory agency interactions
Leading cross-functional teams
Superior communication skills
Problem-solving in matrix environment

Education

Ph.D. or Pharm D in relevant fields
Master's Degree in relevant fields

Job description

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Job Description
General Summary:

The Senior Director, Clinical Pharmacology will serve as a Disease Area leader for Clinical Pharmacology. The Senior Director, Clinical Pharmacology will also manage the scientific functions and coordinate the activities of the Clinical Pharmacology function in collaboration with the other Disease Area leaders. The role’s responsibilities will include maintaining organizational processes across the group, influencing clinical program strategy, and integrating activities with other departments across the Global Research and Development organization, to help shape innovative and integrated clinical development plans. As a Disease Area leader, the Senior Director, Clinical Pharmacology will also direct Clinical Pharmacology efforts for small molecule and novel modality programs, such as gene editing, gene therapy, and cell therapy, in the Disease Area.

Key Duties And Responsibilities
  • Defines the scientific direction and directs the execution of clinical pharmacology plans for Disease Area programs
  • Provides strategic operational leadership to the Clinical Pharmacology function in collaboration with the other Disease Area Leaders
  • Manages a group of Clinical Pharmacologists at Director-level and below to set strategy, develop and execute Clinical Pharmacology plans and studies for Disease Area programs
  • Directs Clinical Pharmacology efforts for small molecule and novel modality programs, such as gene editing, gene therapy, and cell therapy, in the Disease Area.
  • As a people manager within the organization, may have financial accountabilities and human resource responsibilities for assigned staff.
Knowledge And Skills
  • Experience designing clinical pharmacology and pharmacometrics components of filing packages and associated clinical studies
  • Experience with regulatory agency interactions including written responses and IND packages
  • Experience with Early Development Phase, as well as End of Phase 2 and NDA/MAA regulatory
  • Support of drug development programs in all Phases including life-cycle management
  • Different therapeutic modality experience (large molecule, small molecule, etc.)
  • Experience leading cross-functional teams
  • Superior communication skills
  • Ability to solve complex problems while working in a matrix environment
  • Academic or clinical postdoctoral training with significant publication history
Education And Experience

Ph.D. or Pharm D (or equivalent degree) in pharmacokinetics, pharmacometrics, clinical pharmacology or translational development and 15+ years of relevant post-doctoral employment experience, orMasters Degree (or equivalent degree) in pharmacokinetics, pharmacometrics, clinical pharmacology or translational development and 20+ years of relevant employment experience, orTypically requires 5 years of supervisory/management experience

Pay Range

$228,000 - $342,000

Disclosure Statement

The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, experience, and other job-related factors permitted by law.

At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations. From medical, dental and vision benefits to generous paid time off (including a week-long company shutdown in the Summer and the Winter), educational assistance programs including student loan repayment, a generous commuting subsidy, matching charitable donations, 401(k) and so much more.

Flex Designation

Remote-Eligible

Flex Eligibility Status

In this Remote-Eligible role, you can choose to be designated as:

  • Remote: work remotely five days per week and come into the office on occasion – you’re always welcome on-site;
  • or select Hybrid: work remotely up to two days per week;
  • or select On-Site: work five days per week on-site with ad hoc flexibility.
Company Information

Vertex is a global biotechnology company that invests in scientific innovation.

Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at ApplicationAssistance@vrtx.com

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