Talent.com
Associate Director, Program Toxicologist, Translational Medicine
Associate Director, Program Toxicologist, Translational MedicineBlueRock Therapeutics • Cambridge, MA, US
Associate Director, Program Toxicologist, Translational Medicine

Associate Director, Program Toxicologist, Translational Medicine

BlueRock Therapeutics • Cambridge, MA, US
29 days ago
Job type
  • Full-time
Job description

Job Description

Job Description

Who is BlueRock?

BlueRock Therapeutics, a wholly-owned and independently operated subsidiary of Bayer AG, is a leading engineered cell therapy company using its unique CELL+GENE™  platform to direct cellular differentiation and genetically engineer cells to create a new generation of cellular medicines that address large patient populations suffering from neurological, cardiovascular, and immunology diseases.

The convergence of cell biology and genetic engineering is creating fundamental new ways to impact disease. Founded in 2016 to capitalize on these technological breakthroughs, we are advancing our novel  CELL+GENE™  platform to develop, manufacture, and deliver an entirely new generation of authentic and engineered cell therapies across three therapeutic areas : neurology, cardiology, and immunology.

What Are We Doing?

Our foundational science harnesses the ability to create and then direct the differentiation of universal pluripotent stem cells into authentic, functional cells that can be used as allogeneic cellular therapies to treat a broad array of diseases. We can also further engineer these cells, enabling them to produce enzymes, antibodies, and other proteins for additional therapeutic benefit.

We are passionate about delivering on the promise of cellular and gene therapy, shaping the future of cellular medicine, and delivering new therapies to millions of patients with treatment options.

We are seeking individuals who are collaborative, thrive in a fun and dynamic culture, and are steadfast in the commitment to advance cutting-edge cellular therapies to impact patients’ lives.

Description of Position :

It continues to be an exciting time for BlueRock Therapeutics as the company advances cutting edge cellular therapies to positively impact patients’ lives across multiple disease areas.

The Program Toxicologist will be expected to take on a highly visible role with internal and external stakeholders through providing scientific and strategic leadership for nonclinical studies in support of BlueRock’s pipeline. The Program Toxicologist will leverage their expertise in toxicology to advance the company’s development pipeline by working closely with program leads and other subject matter experts. The position will be based in Cambridge, Massachusetts.

Responsibilities

  • Design, execute, interpret, and communicate toxicology strategies in support of the BlueRock pipeline from discovery through development.
  • Partner with Research, CMC, Device, and other cross-functional teams to ensure strategic alignment around study plans and study design
  • Identify safety-related knowledge gaps and propose risk-mitigation plans.
  • Ensure preparation of risk assessments, safety summaries, and other technical documents
  • Ensure nonclinical studies are executed with a high level of scientific rigor in support Program strategy
  • Partner with Toxicology Operations to support study start-up, execution, and timely reporting of results with appropriate interpretation and guidance
  • Develop a relationship with CROs and support Toxicology Operations in CRO oversight
  • Ensure GLP compliance and appropriate conduct of studies
  • Travel to CRO to oversee study execution
  • Collaborate with external experts where needed to support program objectives, including but not limited to pathologists and expert consultants
  • As needed review clinical study protocols and author relevant IND / IB sections
  • Author regulatory submissions and interact with regulatory agencies as needed
  • Collaborate within TMND to ensure broad awareness around nonclinical strategy and input into forward looking plans
  • Prepare written and oral presentations for internal and external dissemination
  • Stay current on the evolving regulatory landscape of cell-based therapies

Minimum Requirements

  • Ph.D. in relevant field
  • Minimum of 4 years toxicology experience in industry
  • Must have direct experience partnering with CROs to deliver nonclinical studies (e.g., biodistribution, tumorigenicity, local tolerability)
  • Knowledge of cell therapy space is a plus
  • American Board of Toxicology (ABT) certification preferred
  • Ability to travel to CRO to oversee study execution
  • We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

    Create a job alert for this search

    Toxicologist • Cambridge, MA, US

    Similar jobs
    Associate Medical Director

    Associate Medical Director

    MBTA • Boston, MA, United States
    Full-time
    The Associate Medical Director is a senior member of the MBTA Occupational Health Services department responsible for assisting oversight of the MBTA Medical Department. This unique role offers the ...Show more
    Last updated: 30+ days ago • Promoted
    Associate Director - ExploR&D External Partnering - Molecule Discovery and Technology Licensing

    Associate Director - ExploR&D External Partnering - Molecule Discovery and Technology Licensing

    Eli Lilly and • Boston, MA, United States
    Full-time
    At Lilly, we unite caring with discovery to make life better for people around the world.We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work...Show more
    Last updated: 29 days ago • Promoted
    Associate Director, Global Regulatory Affairs CMC Devices and Combination Products

    Associate Director, Global Regulatory Affairs CMC Devices and Combination Products

    Alexion Pharmaceuticals • Boston, MA, United States
    Full-time
    The Associate Director of Global Regulatory Affairs Chemistry, Manufacturing, and Controls (GRA-CMC) Devices and Combination Products plays a pivotal role in implementation of global CMC regulatory...Show more
    Last updated: 1 day ago • Promoted
    Associate Director Regulatory Affairs

    Associate Director Regulatory Affairs

    Codon Partners • Boston, MA, United States
    Full-time
    Associate Director Regulatory Affairs.Our client is seeking an experienced Associate Director of Regulatory Affairs to lead clinical regulatory strategy for a portfolio of small-molecule drug progr...Show more
    Last updated: 10 days ago • Promoted
    Associate Director, Clinical Operations

    Associate Director, Clinical Operations

    Alnylam Pharmaceuticals • Cambridge, MA, US
    Full-time
    Associate Director, Clinical Operations.The Associate Director is responsible for leading a team of Global Trial Leaders and Trial Managers within the Study Management Organization.The position is ...Show more
    Last updated: 30+ days ago • Promoted
    Associate Director Strategic Business Planning and Execution, US Medical Affairs

    Associate Director Strategic Business Planning and Execution, US Medical Affairs

    AstraZeneca • Boston, MA, United States
    Full-time
    Are you ready to make a significant impact in the world of rare diseases? As the.Associate Director of Strategic Planning & Execution for US Medical Affairs. Therapeutic Area (TA) Leadership teams t...Show more
    Last updated: 28 days ago • Promoted
    Associate Director, Program Toxicologist, Translational Medicine

    Associate Director, Program Toxicologist, Translational Medicine

    BlueRock Therapeutics • Cambridge, MA, United States
    Full-time
    BlueRock Therapeutics, a wholly-owned and independently operated subsidiary of Bayer AG, is a leading engineered cell therapy company using its unique. The convergence of cell biology and genetic en...Show more
    Last updated: 30+ days ago • Promoted
    Associate Director, Clinical Operations

    Associate Director, Clinical Operations

    EPM Scientific • Boston, MA, United States
    Full-time
    Associate Director, Clinical Operations.K-$215K USD + Bonus | Full-Time | Remote.A fast-growing, clinical-stage biotech is redefining treatment paradigms with cutting-edge bispecific antibody thera...Show more
    Last updated: 20 days ago • Promoted
    Associate Director, Statistical Programming

    Associate Director, Statistical Programming

    Alexion Pharmaceuticals, Inc. • Boston, MA, United States
    Full-time
    Associate Director, Statistical Programming — Join to apply for the Associate Director, Statistical Programming role at Alexion Pharmaceuticals, Inc. The Associate Director of Statistical Programmin...Show more
    Last updated: 26 days ago • Promoted
    Associate Director Strategic Business Planning and Execution, US Medical Affairs

    Associate Director Strategic Business Planning and Execution, US Medical Affairs

    Astrazeneca • Boston, MA, United States
    Full-time
    Are you ready to make a significant impact in the world of rare diseases? As the.Associate Director of Strategic Planning & Execution for US Medical Affairs. Therapeutic Area (TA) Leadership teams t...Show more
    Last updated: 27 days ago • Promoted
    Associate Director, Clinical Program Quality

    Associate Director, Clinical Program Quality

    Mindlance • Cambridge, Massachusetts, United States
    Full-time
    Quick Apply
    Job Title : Associate Director, Clinical Program Quality.Duration : 12+ Months (Possible of Extension).Provides quality assurance oversight of the global clinical research programs in Research and De...Show more
    Last updated: 30+ days ago
    Associate Director Pharmacometrics (PhD / PharmD)

    Associate Director Pharmacometrics (PhD / PharmD)

    Novartis Group Companies • Cambridge, MA, United States
    Full-time
    We are 60 quantitative scientists supporting more than 80 clinical development projects in 10 therapeutic areas every day. As the Associate Director Pharmacometrics, you will drive the pharmacometri...Show more
    Last updated: 30+ days ago • Promoted
    Associate Director – Life Sciences Advisory – Oncology Specialist

    Associate Director – Life Sciences Advisory – Oncology Specialist

    Guidehouse • Boston, MA, United States
    Full-time
    Strategy & Transformation Consulting.Is life sciences in your DNA? Breakthroughs in pharma are helping people live healthier lives, while medical devices enable patients to proactively maintain hea...Show more
    Last updated: 9 days ago • Promoted
    Associate Director, Global Regulatory Lead, Oncology

    Associate Director, Global Regulatory Lead, Oncology

    Takeda • Boston, MA, United States
    Full-time
    At Takeda, we are a forward‑looking, world‑class R&D organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on four therapeutic areas and oth...Show more
    Last updated: 30+ days ago • Promoted
    Associate Director, External Scientific Partnerships – US Medical Affairs

    Associate Director, External Scientific Partnerships – US Medical Affairs

    AstraZeneca GmbH • Boston, MA, United States
    Full-time
    Are you ready to make a difference in the world of rare diseases? As the Associate Director, External Scientific Partnerships, US Medical Affairs, you will be at the forefront of strategic initiati...Show more
    Last updated: 30+ days ago • Promoted
    Associate Director, US HCP Marketing, Medical Education

    Associate Director, US HCP Marketing, Medical Education

    Blueprint Medicines, a Sanofi company • Cambridge, MA, United States
    Full-time
    How will your role help us transform hope into reality?.As Associate Director, US HCP Marketing, Medical Education Lead, you will play a pivotal role in transforming the landscape of systemic masto...Show more
    Last updated: 5 days ago • Promoted
    Director, Clinical Pharmacology Remote - United States

    Director, Clinical Pharmacology Remote - United States

    Day One Biopharmaceuticals • Boston, MA, United States
    Remote
    Full-time
    At Day One, we are focused on advancing first- or best-in-class medicines for childhood and adult diseases with equal intensity. We were founded to address the lack of new therapies resulting from t...Show more
    Last updated: 13 days ago • Promoted
    Associate Director Global Clinical Development Operations Biobanking

    Associate Director Global Clinical Development Operations Biobanking

    Biontech • Cambridge, MA, US
    Full-time
    Associate Director Global Clinical Development Operations Biobanking.Cambridge, US; Gaithersburg, US; New Jersey, US | full time | Job ID : 9857. As an Associate Director of Biobanking, you will take...Show more
    Last updated: 3 days ago • Promoted