Current jobs related to Director, Clinical Pharmacology - Cambridge - AbbVie

  • Principal Scientist

    2 weeks ago


    Cambridge, United States Delphia Therapeutics Full time

    Principal Scientist / Associate Director, In vivo PharmacologyAbout Us:Delphia is a biotechnology company on a mission in the service of patients to pioneer an entirely new field of cancer biology, Activation Lethality, that targets cancer’s vulnerability to oncogene overactivation. Together, we are working to advance first-in-class targeted cancer...

  • Principal Scientist

    2 weeks ago


    Cambridge, United States Delphia Therapeutics Full time

    Principal Scientist / Associate Director, In vivo PharmacologyAbout Us:Delphia is a biotechnology company on a mission in the service of patients to pioneer an entirely new field of cancer biology, Activation Lethality, that targets cancer’s vulnerability to oncogene overactivation. Together, we are working to advance first-in-class targeted cancer...


  • Cambridge, Massachusetts, United States Biogen Full time

    Job Title: Clinical Pharmacology and Pharmacometrics Co-opWe are seeking a highly motivated and detail-oriented co-op to join our Clinical Pharmacology and Pharmacometrics team at Biogen. As a co-op, you will have the opportunity to work on exciting projects and contribute to the development of clinical pharmacology studies.Responsibilities:Learn and...


  • Cambridge, Massachusetts, United States Flagship Ventures Full time

    About Pioneering MedicinesPioneering Medicines is a pioneering initiative of Flagship Pioneering, a firm that conceives, creates, resources, and develops first-in-category life science platform companies to transform human health and sustainability.Job SummaryWe are seeking an experienced leader with deep expertise in drug discovery and development to head...


  • Cambridge, Massachusetts, United States Regeneron Pharmaceuticals Full time

    Job SummaryWe are seeking a highly skilled Associate Director to lead our Quantitative Pharmacology team. As a key member of our research and development team, you will be responsible for providing expert-level pharmacometrics support to our therapeutic focus areas.Key ResponsibilitiesDevelop and implement strategic analyses to support research and...


  • Cambridge, United States Blueprint Medicines Full time

    How will your role help us transform hope into reality? The Director, Clinical Science will provide scientific support for all Clinical Development activities involving the conduct of clinical studies, including: clinical development plans, study design and feasibility, data collection requirements, analysis plans, preparation of meeting materials and...


  • Cambridge, Massachusetts, United States Flagship Ventures Full time

    {"title": "In Vivo Pharmacology Team Lead", "subtitle": "Drive Innovation and Excellence in Biopharmaceutical Development", "content": "At Flagship Pioneering, we are seeking an experienced leader to head our In Vivo Pharmacology team. As a key member of our Pioneering Medicines initiative, you will be responsible for driving the development of novel...


  • Cambridge, Massachusetts, United States Vaxess Technologies Full time

    Scientist, In Vivo PharmacologyVaxess Technologies is a clinical-stage biotech company developing innovative vaccines and therapies using its proprietary MIMIXTM Microneedle Array Patch technology. We are seeking a talented individual with expertise in animal models, pharmacology, and immunology to join our core team of scientists and engineers.Key...


  • Cambridge, Massachusetts, United States Sarepta Therapeutics, Inc. Full time

    Job SummaryThe Director, Clinical Development is a key leadership position responsible for driving the advancement of Sarepta's clinical-stage programs. This individual will lead a clinical sciences team and be accountable for defining strategic priorities and integrating cross-functional input to develop and execute the clinical development plan.Key...


  • Cambridge, United States Third Rock Ventures Full time

    Associate Scientist/Scientist, In vivo pharmacologyA well-funded and highly innovative start up from Third Rock Ventures is emerging out of stealth with a syndicate of marquee investors and is seeking a talented Associate Scientist/Scientist to join the Biology-In vivo pharmacology team. The Associate Scientist/Scientist will serve as the in vivo...


  • Cambridge, United States Third Rock Ventures Full time

    Associate Scientist/Scientist, In vivo pharmacologyA well-funded and highly innovative start up from Third Rock Ventures is emerging out of stealth with a syndicate of marquee investors and is seeking a talented Associate Scientist/Scientist to join the Biology-In vivo pharmacology team. The Associate Scientist/Scientist will serve as the in vivo...


  • Cambridge, United States Third Rock Ventures Full time

    Associate Scientist/Scientist, In vivo pharmacologyA well-funded and highly innovative start up from Third Rock Ventures is emerging out of stealth with a syndicate of marquee investors and is seeking a talented Associate Scientist/Scientist to join the Biology-In vivo pharmacology team. The Associate Scientist/Scientist will serve as the in vivo...


  • cambridge, United States KEMIO Consulting Full time

    *Urgent*Associate Director PKDM – Cambridge, MA or New Jersey 50% home working on offerPharmacology, Pharmacokinetics, PKPD, Clinical, Modelling & Simulation, Drug Development KEMIO are working with a global pharmaceutical company buiilding on their capabilities in Pharmacokinetics, Dynamics, and Metabolism. This Associate Director role will be based...


  • Cambridge, United States KEMIO Consulting Full time

    *Urgent*Associate Director PKDM – Cambridge, MA or New Jersey 50% home working on offerPharmacology, Pharmacokinetics, PKPD, Clinical, Modelling & Simulation, Drug Development KEMIO are working with a global pharmaceutical company buiilding on their capabilities in Pharmacokinetics, Dynamics, and Metabolism. This Associate Director role will be based...


  • Cambridge, United States KEMIO Consulting Full time

    *Urgent*Associate Director PKDM – Cambridge, MA or New Jersey 50% home working on offerPharmacology, Pharmacokinetics, PKPD, Clinical, Modelling & Simulation, Drug Development KEMIO are working with a global pharmaceutical company buiilding on their capabilities in Pharmacokinetics, Dynamics, and Metabolism. This Associate Director role will be based...


  • Cambridge, United States KEMIO Consulting Full time

    *Urgent*Associate Director PKDM – Cambridge, MA or New Jersey 50% home working on offerPharmacology, Pharmacokinetics, PKPD, Clinical, Modelling & Simulation, Drug Development KEMIO are working with a global pharmaceutical company buiilding on their capabilities in Pharmacokinetics, Dynamics, and Metabolism. This Associate Director role will be based...


  • Cambridge, Massachusetts, United States Sarepta Therapeutics, Inc. Full time

    Job SummaryThe Director, Clinical Development is a key leadership position responsible for leading a clinical sciences team that drives the advancement of Sarepta's clinical-stage programs. This individual will define strategic priorities for the program, integrate cross-functional input, and develop and execute the clinical development plan.Key...


  • Cambridge, Massachusetts, United States Sarepta Therapeutics, Inc. Full time

    Job SummaryThe Director, Clinical Development is a key leadership position responsible for driving the advancement of Sarepta's clinical-stage programs. This individual will lead a clinical sciences team, defining strategic priorities and integrating cross-functional input to develop and execute the clinical development plan.Key ResponsibilitiesDevelop and...


  • Cambridge, United States Vaxess Technologies Full time

    Location: Cambridge, MAVaxess Technologies is developing next generation vaccines and therapies based on its proprietary MIMIXTM Microneedle Array Patch technology. MIMIXTM enables self-administration of vaccines and therapeutics to the skin with potential for improved shelf-stability, tolerability, and efficacy. We are committed to enabling products that...


  • Cambridge, United States Vaxess Technologies Full time

    Location: Cambridge, MAVaxess Technologies is developing next generation vaccines and therapies based on its proprietary MIMIXTM Microneedle Array Patch technology. MIMIXTM enables self-administration of vaccines and therapeutics to the skin with potential for improved shelf-stability, tolerability, and efficacy. We are committed to enabling products that...

Director, Clinical Pharmacology

3 months ago


Cambridge, United States AbbVie Full time

Company Description

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas immunology, oncology, neuroscience, and eye care and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us atwww.abbvie.com. Follow @abbvie onTwitter,Facebook,Instagram,YouTubeandLinkedIn.

Job Description

As a Director within the Clinical Pharmacology Neuroscience Group at AbbVie, you will lead clinical pharmacology programs in the Neuroscience/Psychiatry drug development area. You will have a seat at the table within asset teams to influence, decide, and recommend key clinical pharmacology strategies and information. You will be responsible and accountable for a variety of programs across the drug development spectrum, ranging from first in human through approval, including life cycle management and post approval commitments/requirements. You will be expected to communicate/present and lead key Clinical Pharmacology information/strategy to senior and executive management, regulatory agencies, and external peers. In your role, you will lead strategic planning for drug development activities and projects to achieve departmental strategies, goals, and objectives. Utilizing scientific expertise to provide appropriate interpretation of data to relate implications of results to asset teams and management. You will serve as liaison to other departments/divisions for any study/project needs, influence and strategically manage linkages across businesses and understand the impact of business decisions and solutions. You will be expected to lead teams within Clinical Pharmacology and be accountable for effective performance of the teams.

Responsibilities

  • Independently leads Clinical Pharmacology/PK/PD activities and multiple major projects. Assists asset teams and R&D senior management in the selection of action plans that best meets drug development business objectives.
  • Identifies issues impacting multiple complex projects and leads issue resolution. Conducts risk assessments and leads the function in development of contingency plans. Assures project remains in alignment with strategic objectives.
  • Provides overall clinical pharmacology timelines to assess portfolio opportunities. Negotiates with other functional areas on project outcomes and deliverables to meet conflicting demands (time, cost, quality/performance).
  • Provides expert scientific and strategic consultation to R&D teams, Regulatory, and all levels of management on critical decisions and development plans. Connects scientific, regulatory, and business implications from multiple teams. Influences and strategically manages linkages across businesses and understands the impact of business decisions and solutions.
  • Responsible for critically evaluating technical, scientific aspects of all AbbVie projects along with CLINICAL PHARMACOLOGY management. Reviews clinical protocols and scientific reports for regulatory filings and anticipates regulatory questions. Leads CLINICAL PHARMACOLOGY regulatory documents writing, submission and response to Regulatory agency comments.
  • Independently conducts due diligence assessments, summarizes results and represents CLINICAL PHARMACOLOGY on business development teams.
  • Identifies and develops process improvement initiatives and reviews recommendations with management for approval and sponsorship.
  • Responsible for leading efforts to develop departmental goals. Makes strategic clinical PK/PD decisions for the department. Provides leadership on strategic clinical pharmacology and drug development.
  • Manages personnel including development, mentoring, and effective delegation.
  • Leads teams within department, across CLINICAL PHARMACOLOGY and across functions. Responsible for leadership of cross-functional teams and accountable for effective performance of the team. Actively manages project team behaviors, mediates internal team disputes, and facilitates establishment of healthy and high performing teams.

Qualifications

Qualifications

  • PhD with typically 9+ years of experience or PharmD with typically 11+ years of experience in a relevant field (*relevant field includes experience with PK, PBPK, PK-PD, Pharmacometrics or systems pharmacology, Drug metabolism/Transporters)
  • Excellent interpersonal skills
  • Advanced knowledge and experience in multiple therapeutic and/or functional areas
  • Experience across range of development phases
  • Recognized as an expert with global knowledge of AbbVie and Pharma drug development processes
  • Must have demonstrated strong leadership competencies in Clinical Pharmacology, PK/PD, Biopharmaceutics, and Pharmacometric activities from planning, implementation through completion across multiple complex projects
  • Demonstrated leadership skills with broad scientific and business-related orientations
  • Demonstrated project management skills such as scope management, progress tracking/driving as well as people and time management
  • Key contributor to initiatives and advancement of CLINICAL PHARMACOLOGY
  • Key Leadership Competencies:
    • Knows the business and the cross-functional contributions needed to deliver results
    • Manages conflict and difficult conversations in a constructive transparent way
    • Develops direct reports and capable successors through coaching, stretch assignments and learning opportunities
    • Respectfully provides transparent, accurate and timely feedback to help direct reports improve performance
    • Creates an inclusive environment where all direct reports can succeed

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:

  • The compensation range described below is the range of possible base pay compensation that the Company believesingood faith it will pay for this role at the time of this posting based on the job grade for this position.Individualcompensation paid within this range will depend on many factors including geographic location, and we mayultimatelypay more or less than the posted range. This range may be modified in the future.

  • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),medical/dental/visioninsurance and 401(k) to eligible employees.

  • This job is eligible to participate in our short-term incentive programs.

  • This job is eligible to participate in our long-term incentive programs.

Note: No amount of payis considered to bewages or compensation until such amount is earned, vested, anddeterminable.The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensationand benefitsthat are allocable to a particular employee remains in the Company's sole and absolute discretion unless anduntil paid andmay be modified at the Companys sole and absolute discretion, consistent with applicable law.

AbbVie is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVies policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.