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Become A Director, Clinical Pharmacology

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Working As A Director, Clinical Pharmacology

  • Getting Information
  • Analyzing Data or Information
  • Identifying Objects, Actions, and Events
  • Updating and Using Relevant Knowledge
  • Documenting/Recording Information
  • Mostly Sitting

  • $64,000

    Average Salary

What Does A Director, Clinical Pharmacology Do At Washington University of St. Louis

* With principal investigator, designs, performs and evaluates research procedures.
* Assists with grant preparation and journal article submission.
* Develops and implements policies and procedures.
* Provides comprehensive direction to laboratory personnel.
* Hires, trains and evaluates the performance of laboratory personnel.
* Oversees and directs all support activities of the lab including human resources, budgets, facility maintenance, purchasing, supplies, materials and equipment.
* Researches and recommends new methods and procedures to maintain current capabilities, quality and standards

What Does A Director, Clinical Pharmacology Do At Bristol Myers Squibb

* The Clinical Pharmacology & Pharmacometrics (CP&P) department is searching for a Principal Scientist with expertise in Pharmacometrics (Pm) and Model
* Based Meta
* Analysis (MBMA).
* The Principal Scientist will join the Quantitative Clinical Pharmacology (QCP) group to conduct Pm analyses that will facilitate model-based drug development.
* This individual will be responsible for: (1) collaborating with cross-functional team members to help address key program and portfolio level questions, (2) developing and implementing Pm/MBMA analysis strategies to address key questions, (3) ensuring alignment of the Pm/MBMA strategy with the global clinical development plan, (4) reporting and interpretation of Pm/MBMA analysis results, (5) contributing to Clinical Pharmacology regulatory submissions (pre- and post-approval), (6) serving as a Pm and MBMA expert for both internal colleagues and to the external scientific clinical pharmacology/pharmacometrics community.
* This position will provide an opportunities for internal and external growth/leadership in both Pm and Clinical Pharmacology

What Does A Director, Clinical Pharmacology Do At Cytokinetics

Design Phase I and Phase IIa clinical studies, including dose escalation, stopping rules and risk-benefit to ascertain that compounds are entered into man safely, efficiently and with scientific validityResponsible for the medical content of clinical pharmacology studiesResponsible for the medical aspects of clinical pharmacology components related to regulatory documents and interact with regulatory authorities for all phases of drug developmentMedical monitor in sponsored studies as appropriate, ensure that the clinical teams correctly handle all adverse events (AEs) and serious adverse events (SAEs) in accordance with ICH standardsCorrectly apply the ICH and GCP regulations surrounding the primary activities of clinical development projectsOperate within the time and budget constraints of the clinical programIn collaboration with the Chief Medical Officer, train members of the product development team to enhance their skillsCommunicate project-related information, including the planning and execution of meetings and presentationsCoordinate and complete scientific documents including protocols, clinical study reports, other regulatory documentsTravel up to 30% as necessary according to project needs

What Does A Director, Clinical Pharmacology Do At Celgene

* Plan and execute clinical pharmacology studies
* Provide strategic direction and/or hands-on support to the writing and review of study synopses, protocols, and clinical study reports
* Perform data analyses including NCA, population PK and exposure-response
* Work with statisticians and team members to interpret and report study results
* Contribute to the regulatory submission packages, and participate in regulatory meetings as appropriate
* Collaborate with Preclinical Research and Translational Medicine on biomarker strategies and preclinical model selection and study design
* Serve as a clinical study team leader for clinical pharmacology studies
* Articulate clinical pharmacology plans and study results to development teams and/or senior management
* Present study results at scientific conferences and in scientific journals
* Other responsibilities as assigned
* Celgene is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.
* Celgene complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act.
* All applicants must have authorization to work for Celgene in the U
* S

What Does A Director, Clinical Pharmacology Do At Sanofi Group

* Participate in designing the early development plan and overall translational medicine and clinical pharmacology plan for the different steps of clinical development, according to the strategy developed by the Company.
* Review, interpret results, and author translational medicine and clinical pharmacology-related clinical documentation, including: clinical protocols, study reports; some abstracts and/or manuscripts; clinical pharmacology components of investigator brochures, regulatory documents.
* Interacts effectively with managers from various disciplines; serves as expert and internal consultant on assigned area and liaises with partners on projects.
* Coordinates the translational medicine subteam meetings.
* Coordinates activity of the clinical study director of assigned project(s).
* Participates in the dose selection for first-in-human studies, Go/No Go decisions when needed.
* Ensures an adequate follow-up of studies and project timelines.
* Communicates project team discussions of interest to the other group members who are involved with the project.
* Presents data in appropriate meetings (inside or outside the Group).
* Interactions:
* Internal: Scientists, clinicians, and project leaders in therapeutic areas, clinical trial managers, data managers, study biostatisticians, representatives from Regulatory Affairs, Safety & Toxicology, Global Pharmacovigilance & Epidemiology (GPE)
* External: investigators, clinical experts, clinical research organizations, health authorities.
* Major Challenges and opportunities:
* Communication of the role of the department; requires a committed and enthusiastic person to emphasize the strengths of the position and a positive, collaborative attitude.
* Takes an active part in the scientific challenges involved in early clinical development, which require a scientifically inquisitive, energetic and proactive person.
* Ensures Clinical Trial standards are maintained at the site and in cooperation with the other clinical functions.
* Requires excellent communication skills and the implementation of an appropriate process for communication.
* Ensures high quality documents, requiring strong writing and communication skills.
* Manages aggressive timelines effectively through cross-functional planning.
* Key Internal/External Relationships:
* Internal contacts: Clinical trial operations, data management coordinators, group leaders, department head.
* External contacts: Company departments and enabling functions

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How To Become A Director, Clinical Pharmacology

Medical scientists typically have a Ph.D., usually in biology or a related life science. Some medical scientists get a medical degree instead of a Ph.D., but prefer doing research to practicing as a physician.

Education

Students planning careers as medical scientists typically pursue a bachelor’s degree in biology, chemistry, or a related field. Undergraduate students benefit from taking a broad range of classes, including life sciences, physical sciences, and math. Students also typically take courses that develop communication and writing skills, because they must learn to write grants effectively and publish research findings.

After students have completed their undergraduate studies, they typically enter Ph.D. programs. Dual-degree programs are available that pair a Ph.D. with a range of specialized medical degrees. A few degree programs that are commonly paired with Ph.D. studies are Medical Doctor (M.D.), Doctor of Dental Surgery (D.D.S.), Doctor of Dental Medicine (D.M.D.), and Doctor of Osteopathic Medicine (D.O.). Whereas Ph.D. studies focus on research methods, such as project design and data interpretation, students in dual-degree programs learn both the clinical skills needed to be a physician and the research skills needed to be a scientist.

Graduate programs emphasize both laboratory work and original research. These programs offer prospective medical scientists the opportunity to develop their experiments and, sometimes, to supervise undergraduates. Ph.D. programs culminate in a thesis that the candidate presents before a committee of professors. Students may specialize in a particular field, such as gerontology, neurology, or cancer.

Those who go to medical school spend most of the first 2 years in labs and classrooms, taking courses such as anatomy, biochemistry, physiology, pharmacology, psychology, microbiology, pathology, medical ethics, and medical law. They also learn how to record medical histories, examine patients, and diagnose illnesses. They may be required to participate in residency programs, meeting the same requirements that physicians and surgeons have to fulfill.

Medical scientists often continue their education with postdoctoral work. Postdoctoral work provides additional and more independent lab experience, including experience in specific processes and techniques such as gene splicing, which is transferable to other research projects.

Licenses, Certifications, and Registrations

Medical scientists primarily conduct research and typically do not need licenses or certifications. However, those who administer drugs, gene therapy, or otherwise practice medicine on patients in clinical trials or a private practice need a license to practice as a physician.

Important Qualities

Communication skills. Communication is critical, because medical scientists must be able to explain their conclusions. In addition, medical scientists write grant proposals, because grants often are required to fund their research.

Critical-thinking skills. Medical scientists must use their expertise to determine the best method for solving a specific research question.

Data-analysis skills. Medical scientists use statistical techniques, so that they can properly quantify and analyze health research questions.

Decisionmaking skills. Medical scientists must determine what research questions to ask, how best to investigate the questions, and what data will best answer the questions.

Observation skills. Medical scientists conduct experiments that require precise observation of samples and other health data. Any mistake could lead to inconclusive or misleading results.

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Director, Clinical Pharmacology jobs

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Director, Clinical Pharmacology Demographics

Gender

  • Male

    69.1%
  • Female

    29.1%
  • Unknown

    1.8%

Ethnicity

  • White

    70.9%
  • Hispanic or Latino

    13.9%
  • Asian

    11.9%
  • Unknown

    2.8%
  • Black or African American

    0.5%
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Languages Spoken

  • French

    100.0%

Director, Clinical Pharmacology

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Director, Clinical Pharmacology Education

Director, Clinical Pharmacology

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Real Director, Clinical Pharmacology Salaries

Job Title Company Location Start Date Salary
Executive Director, Clinical Pharmacology and Drug Forest Research Institute, Inc. Jersey City, NJ Oct 01, 2011 $297,440
Head of Clinical Pharmacology Regeneron Pharmaceuticals, Inc. Tarrytown, NY Oct 06, 2014 $270,000
Director Clinical Pharmacology/Pharmacodynamics Oncology Bayer Healthcare Pharmaceuticals NJ Jul 12, 2016 $233,000
Director, Dmpk and Clinical Pharmacology Verastem Needham, MA Feb 02, 2016 $160,000 -
$170,000
Director, Clinical Pharmacology and Dmpk Verastem, Inc. Needham, MA Sep 09, 2014 $160,000
Director, Clinical Pharmacology Millennium Pharmaceuticals, Inc. Cambridge, MA Jun 21, 2010 $155,000
Associate Director, Clinical Pharmacology Statisti Novartis Pharmaceuticals Corporation East Hanover, NJ Nov 02, 2014 $151,373
Assistant Director-Clinical Pharmacology Abbott Laboratories Parkersburg, IL Oct 01, 2011 $144,659
Assistant Director, Clinical Pharmacology Abbott Laboratories Parkersburg, IL Dec 27, 2010 $143,510
Associate Director, Clinical Pharmacology Dmpk Endo Pharmaceuticals, Inc. Malvern, PA Apr 04, 2016 $140,000
Associate Director, Clinical Pharmacology Pfizer Inc. Groton, CT Jun 20, 2011 $137,500 -
$206,400
Associate Director, Clinical Pharmacology Pfizer Inc. New London, CT Dec 20, 2010 $137,500 -
$206,400

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Top Skills for A Director, Clinical Pharmacology

ClinicalPharmacologyStudiesRegulatorySubmissionsClinicalDevelopmentFDAOncologyClinicalTrialsImidCross-ValidationApproachINDCNSAnimalModelsAssayValidationRareCellEnrichmentGLPCopdRMapkPHDCyclinD1TherapeuticAreas

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Top Director, Clinical Pharmacology Skills

  1. Clinical Pharmacology Studies
  2. Regulatory Submissions
  3. Clinical Development
You can check out examples of real life uses of top skills on resumes here:
  • Championed three research projects (fertility and men's urology) and which have advanced to Phase III clinical development.
  • Represented clinical pharmacology at the FDA meetings and teleconferences on Overactive Bladder.
  • Managed and supervised 10 Clinical Research Managers/Specialists that implemented/executed Clinical Programs in Oncology therapeutic area.
  • Prepared confidentiality letters and agreements to initiate Clinical Trials.
  • Prepared lectures, practice questions and cases, and individualized additional material for struggling students

Top Director, Clinical Pharmacology Employers