Senior Clinical Research Scientist

October 19

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Cullinan Oncology

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Oncology

11 - 50

💰 $10M Post-IPO Equity on 2022-03

Description

• Cullinan Therapeutics, Inc. (Nasdaq: CGEM) is a biopharmaceutical company dedicated to creating new standards of care for patients. • We have strategically built a diversified portfolio of clinical-stage assets that inhibit key drivers of disease or harness the immune system to eliminate diseased cells in both oncology and autoimmune disease. Our portfolio encompasses a wide range of modalities, each with the potential to be best and/or first in class. • Anchored in a deep understanding of oncology, immunology, and translational medicine, we create differentiated ideas, identify the most appropriate targets, and select the optimal modality to develop transformative therapeutics across a wide variety of cancer and autoimmune indications. • We push conventional boundaries from candidate selection to differentiated therapeutic, applying rigorous go/no go criteria at each stage of development to fast-track only the most promising molecules to the clinic and, ultimately, commercialization. • With deep scientific expertise, our teams exercise creativity and urgency to deliver on our promise to bring new therapeutic solutions to patients. • The Clinical Research Scientist participates in the execution of clinical development programs in collaboration with other clinical development team members, including medical, clinical operations, translational sciences, and regulatory affairs. The Clinical Research Scientist will play an essential role in developing clinical and regulatory documents, reviewing scientific and clinical data, and communicating data both within the company and outside scientific and medical audiences.

Requirements

• Advanced degree in life sciences and/or health-related field, with 5+ years of drug development experience or bachelor’s level education with equivalent working experience • Basic knowledge of medical oncology and oncology clinical trials including RECIST Criteria • Strong understanding of Good Clinical Practice, the drug development process, and the design and conduct of clinical trials. Experience in conducting trials in oncology will be preferred • Excellent written and verbal communication skills • Ability to interact with staff at all levels to coordinate and execute study activities in a fast-paced small biotech environment • Passion and dedication to clinical research