(Associate) Director, Clinical Scientist

IMMUNEERING CORPORATION • Cambridge, MA

51d • Remote

About The Position

Key Responsibilities

• Provide scientific and strategic leadership in the planning and execution of clinical trials, including protocol development, study design, and data analysis.

• Author and review clinical protocols, ICFs, CSRs and regulatory documents

• Collaborate closely with cross-functional teams, including Clinical Operations, Regulatory Affairs, Biostatistics, and Medical Affairs, to ensure the successful conduct of clinical studies.

• Interpret clinical data, prepare study reports, and contribute to regulatory submissions and presentations for internal and external stakeholders.

• Support investigator meetings, advisory boards and data monitoring committee meetings

• Stay current with emerging scientific literature, competitive landscape, and regulatory requirements relevant to Immuneering’s oncology therapeutic area.

• Support the development of clinical development plans and contribute to the strategic direction of ongoing and future programs.

• Work closely with CRO’s and have a can do, proactive biotech mindset.

Requirements

• PhD, PharmD, RN, or MD in a relevant scientific discipline (e.g., biology, pharmacology, medicine).
• Minimum of 5-8 years of experience in clinical development within the pharmaceutical or biotechnology industry.
• Direct Phase 3 oncology clinical trial experience required.
• Demonstrate experience authoring and reviewing clinical documents.
• Demonstrated strong experience in clinical trial execution and data interpretation.
• Strong analytical, organizational, and communication skills.
• Deep understanding of oncology clinical development, endpoints and regulatory expectations.

Responsibilities

• Provide scientific and strategic leadership in the planning and execution of clinical trials, including protocol development, study design, and data analysis.
• Author and review clinical protocols, ICFs, CSRs and regulatory documents
• Collaborate closely with cross-functional teams, including Clinical Operations, Regulatory Affairs, Biostatistics, and Medical Affairs, to ensure the successful conduct of clinical studies.
• Interpret clinical data, prepare study reports, and contribute to regulatory submissions and presentations for internal and external stakeholders.
• Support investigator meetings, advisory boards and data monitoring committee meetings
• Stay current with emerging scientific literature, competitive landscape, and regulatory requirements relevant to Immuneering’s oncology therapeutic area.
• Support the development of clinical development plans and contribute to the strategic direction of ongoing and future programs.
• Work closely with CRO’s and have a can do, proactive biotech mindset.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Ph.D. or professional degree