TANNER & ASSOC INC
Atara Biotherapeutics : Director, Clinical Research and Developme...
TANNER & ASSOC INC - South San Francisco, California, us, 94083
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Overview
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Overview
Atara Biotherapeutics is seeking a
Director of Clinical Research and Development (Immuno-Oncology – Hematology / Oncology) . Position:
Director, Clinical Research and Development (Immuno-Oncology – Hematology / Oncology) Company:
Atara Biotherapeutics Mission:
To develop novel treatments for patients with severe, life-threatening conditions underserved by scientific innovation, focusing on biotech-derived therapies targeting unique pathways. Position Summary: The Director will support the growth of Atara's pipeline in immuno-oncology and hematology-oncology by designing clinical trials to evaluate efficacy, safety, pharmacology, and pharmacokinetics of biologic and cellular immunotherapies. The role includes managing collaborations with academic institutions and consultants and requires a passion for all aspects of clinical drug development. Reports to:
Chief Medical Officer Location:
Thousand Oaks, CA (preferred), South San Francisco, CA (possible) Responsibilities: Design and optimize clinical trials for immuno-oncology and biologic therapies, including protocols, amendments, investigator brochures, reports, abstracts, and manuscripts. Serve as medical monitor, evaluating safety, pharmacology, and efficacy in studies. Develop and implement biomarker plans in collaboration with staff and partners. Engage with investigators, thought leaders, advisory boards, and internal teams. Ensure compliance with SOP standards. Maintain scientific awareness in relevant areas. Travel:
Up to 25% travel may be required. Qualifications: MD or MD / PhD with advanced training in hematology, oncology, or immunology; board certification preferred. At least 2 years of industry experience in clinical studies for solid tumors, hematologic malignancies, or immuno-oncology. Understanding of drug development, GCP, FDA regulations, and regulatory requirements. Strong communication skills, capable of explaining complex technical issues to diverse audiences. Independent work capability and experience in fast-paced, team environments. Strong clinical, scientific, technical, and organizational skills. Effective problem-solving, motivation, teamwork, and project management skills. Note: This job posting appears active; no indications of expiration are present.
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Director of Clinical Research and Development (Immuno-Oncology – Hematology / Oncology) . Position:
Director, Clinical Research and Development (Immuno-Oncology – Hematology / Oncology) Company:
Atara Biotherapeutics Mission:
To develop novel treatments for patients with severe, life-threatening conditions underserved by scientific innovation, focusing on biotech-derived therapies targeting unique pathways. Position Summary: The Director will support the growth of Atara's pipeline in immuno-oncology and hematology-oncology by designing clinical trials to evaluate efficacy, safety, pharmacology, and pharmacokinetics of biologic and cellular immunotherapies. The role includes managing collaborations with academic institutions and consultants and requires a passion for all aspects of clinical drug development. Reports to:
Chief Medical Officer Location:
Thousand Oaks, CA (preferred), South San Francisco, CA (possible) Responsibilities: Design and optimize clinical trials for immuno-oncology and biologic therapies, including protocols, amendments, investigator brochures, reports, abstracts, and manuscripts. Serve as medical monitor, evaluating safety, pharmacology, and efficacy in studies. Develop and implement biomarker plans in collaboration with staff and partners. Engage with investigators, thought leaders, advisory boards, and internal teams. Ensure compliance with SOP standards. Maintain scientific awareness in relevant areas. Travel:
Up to 25% travel may be required. Qualifications: MD or MD / PhD with advanced training in hematology, oncology, or immunology; board certification preferred. At least 2 years of industry experience in clinical studies for solid tumors, hematologic malignancies, or immuno-oncology. Understanding of drug development, GCP, FDA regulations, and regulatory requirements. Strong communication skills, capable of explaining complex technical issues to diverse audiences. Independent work capability and experience in fast-paced, team environments. Strong clinical, scientific, technical, and organizational skills. Effective problem-solving, motivation, teamwork, and project management skills. Note: This job posting appears active; no indications of expiration are present.
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