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Director, Bioanalytical and Biomarker Development my client company, a very dynamic and growing biotech organization is seeking an experienced and highly technical scientist to join their Bioanalytical/Biomarker team. This strong leader will develop and put into place bioanalytical and biomarker strategies with a robust pipeline with programs that are in early through mid-stage. Some of these will be nucleic acid based. This is the perfect position for an individual with a strong background in


Sr. VP, Regulatory Affairs The Sr. Vice President of Regulatory Affairs will be responsible for all aspects of Regulatory Affairs related to clinical development, CMC and commercialization. This person will be responsible for leading the strategic direction and operational aspects of global regulatory compliance and submissions for all projects across the company. Create and implement a regulatory strategy and related activities for approvalsDevelop and implement strategies for submissions and


In this senior leadership role, the successful candidate will have many opportunities to make meaningful contributions and be instrumental in setting the strategic direction for drug discovery and development at the company. The successful candidate will become the point of accountability for target validation, in vivo pharmacology and lead development. The candidate must have senior leadership experience in oncology discovery, development or translational research in the....


My client in Massachusetts is seeking an experienced DMPK scientist to join their Drug Metabolism and Pharmacokinetic Group. The successful candidate will be highly skilled with drive to evaluate and implement state-of-art in vitro technologies to assess drug-drug interaction potential of compounds. Supporting small molecule programs from early discovery to Phase II the successful candidate will bring expertise in CYP inhibition, CYP induction, drug transporter and other cell-based assays.....


Senior Director of CMC My client, an exciting pharmaceutical company in the clinical stage of development, is seeking a very experienced small molecule CMC Senior Director to join their team. To be considered you must have a strong CMC background with expertise in executing product development strategies for small molecule development. This experience will span from preclinical projects all the way through late-stage clinical development and NDA filings. You will be driving and managing....


Project Manager, Drug Development The person selected for this role will be responsible for supporting the coordination, oversight and management of drug product development projects. This will including monitoring project status, timelines and budgets. You must have previously worked with other functional groups within the cross-functional areas– Nonclinical, CMC, Clinical, Regulatory Affairs, etc. – and be able to anticipate changes within the project and how these changes will affect the....


Manager of QC My client is an exciting biopharmaceutical organization with programs in development for small molecules and protein therapeutics! They are seeking a Manager of Quality Control who will work cross-functionally with various departments and will oversee activities that will support commercial products. As a manager, you must have a strong technical background in development and manufacturing for small molecule drug substance and drug product. This manager of Quality Control must....


My client is a clinical-stage biotechnology company focused on the discovery and development of therapeutics for rare genetic diseases. The company is extremely well-funded and growing. If you are a passionate, DMPK scientist eager to make an impact this is an exciting time to join this organization. Title: Sr. Scientist In this role you will bring expertise to design, execute and analyze drug metabolism and pharmacokinetic studies. As DMPK representative to project teams you will provide DMPK


The successful candidate will join an expanding nonclinical drug development department in this growing company. In this role, she/he will be responsible for the design, conduct, and interpretation of nonclinical studies and serve as the toxicology representative to project teams. She/he will play an important role in planning and designing of regulatory toxicology studies and contribute to toxicology strategy. Oversight and coordination of outsourced work with CROs. Responsible for writing....


A California based company, focused on creating advanced and novel medicines for treating patients with unmet medical needs using current cutting-edge RNA targeted technologies, is looking for a new Executive Director of Clinical Development in Neurology. This is an exciting leadership opportunity in a challenging, motivating and rewarding environment. This candidate will have their MD, PharmD or PhD and will enjoy “rolling up their sleeves and getting involved with their team.” They will be....


Senior Principle Investigator, Anatomic Pathology As a key member of the Preclinical Safety Assessment department the successful candidate will be highly visible in a global function capacity responsible for the design and conduct of nonclinical safety programs for the comprehensive safety assessment of novel therapies. This involvement is at all stages of drug discovery and development process. Working within a matrix environment she/he will develop appropriate pathology strategy for a full....


In this scientific leadership role the Director of Toxicology will be responsible for developing strategic plans for drug development programs. The successful candidate will provide in depth toxicology and safety pharmacology expertise designing studies, interpreting data, and implementation of strategic plans for nonclinical development. Actively participating on project teams, the successful candidate will collaborate with drug discovery scientists, including developing new initiatives as....


Title: Fellow (Toxicology) In this leadership role you will be responsible for nonclinical safety programs for the comprehensive safety assessment of therapies at all stages of discovery and development. In this role you will bring your expertise to support the drug development process of novel compounds. Using cutting edge science and technologies you will perform robust assessments of novel therapies for the treatment of the most serious diseases bringing better treatment to patients. The....


In this leadership role, the Director of Pathology will provide significant intellectual and strategic input for discovery and drug development programs. With responsibility for all pathological aspects of preclinical safety studies, you will provide key pathology contributions to project teams and guide project-related pathology support and investigative efforts. Functioning as a key study pathologist/toxicologist on preclinical safety and pharmacology studies, the successful candidate will....

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