Project Manager, PreClinical Safety - Watertown, MA

Job summary · We're looking for a motivated and proactive Project Manager (Contractor) to track operations within the Preclinical Safety Team encompassing discovery through IND-enabling and other development related activities for Toxicology, Drug Metabolism, and Pharmacokinetics ...

We're looking for a motivated and proactive Project Manager to drive operations within the Preclinical Safety Team encompassing discovery R&D through IND-enabling and other development-related activities. · ...

+We are looking for a motivated and proactive Project Manager (Contractor) to track operations within the Preclinical Safety Team. · +Study Timeline Tracking: Collaborate with internal/external team representatives and project managers to assist in the tracking timelines and repo ...

We're looking for a motivated and proactive Project Manager to drive operations within the Preclinical Safety Team. · Study Planning and Scheduling: Collaborate with internal/external team representatives. · ...

We are seeking an experienced scientific leader to head our new Preclinical Safety and Toxicology team within the Integrated DMPK & Safety organisation. · In this senior leadership role, you will provide strategic direction for Orion Pharma's Preclinical Safety & Toxicology funct ...

+The Vertex Preclinical Safety Assessment internship program is a multi-week experiential training program for students passionate about science and eager to learn. · * Contribute to the development of in vitro assays to support the selection and de-risking of potential drug cand ...

We're seeking an intern to join our In Vitro Toxicology team located in Boston, MA.This individual will contribute to designing preclinical in vitro models to assess potential drug candidates throughout the drug discovery process. · The ideal candidate will have strong wet-lab sk ...

Kickstart your career at Vertex by working on meaningful projects, collaborating with talented teams, and learning from industry leaders. · ...

We are seeking an experienced Senior Project Manager to join Mariana's Chemistry Manufacturing & Controls organization advancing personalized medicine and radiopharmaceuticals. · Manage end-to-end planning coordination and execution of radiochemistry team activities supporting pr ...

Acrivon is currently advancing its lead program ACR-368 a selective small molecule inhibitor targeting CHK1 and CHK2 in a potentially registrational Phase 2b trial for endometrial cancer The company has received Fast Track designation from the Food and Drug Administration or FDA ...

The Principal Scientist/ Associate Director/Director will be a key member of Acrivon Therapeutics Clinical Development team and assist our clinical science efforts to: · S · upport the development of two clinical stage assets currently being evaluated in cancer patients (ACR-368 ...

Job summary · This is an experienced Scientist I/II position in the radiochemistry department of Mariana Oncology. The job involves radiochemistry development and troubleshooting with various isotopes for personalized medicine and radiopharmaceuticals. · ResponsibilitiesRadiolabe ...

Join the team protecting half a billion lives every year with next-gen science, mRNA innovation, · and AI-driven breakthroughs. · ...

The Antibiotic Discovery Center (ADC) is seeking an experienced Associate Research Scientist to lead and expand efforts in natural product–based antibiotic discovery. · Lead discovery and characterization of novel natural products with antibacterial or other bioactive properties. ...

The Director, Clinical Quality Assurance leads GCP compliance and quality oversight for clinical programs and commercial products.This role is responsible for developing and implementing risk-based strategies; managing audits, inspections, and vendor oversight; and ensuring globa ...

Associate Director in Nonclinical Safety Evaluation designing and implementing nonclinical safety assessment strategies. · * Design and implement nonclinical safety assessment strategies* Communicate strategies and findings internally and to regulatory authorities globally · * Al ...

Crescent Biopharma's vision is to build a world leading oncology company bringing the next wave of therapies for cancer patients. · The Company's clinical-stage pipeline includes its lead program, a PD-1 x VEGF bispecific antibody, as well as novel antibody-drug conjugates. By le ...

The Director, Clinical Quality Assurance leads GCP compliance and quality oversight for clinical programs and commercial products. · This role is responsible for developing and implementing risk-based strategies; managing audits, inspections, and vendor oversight; and ensuring gl ...

The Director, Clinical Quality Assurance leads GCP compliance and quality oversight for clinical programs and commercial products. · Bachelor's degree in a scientific, allied health, or medical field required; Master's degree preferred · ...

Job summary · The US West Medical Science Liaison Director at Zenas is a key Medical Affairs leader responsible for hiring and managing a high-performing team of Medical Science Liaisons. · Field Team Leadership & Development · Manage (recruit, train, coach, and mentor) a team of ...