Remote Oncology Clinical Scientist, Associate Director

Candel Therapeutics, Inc.; Needham (MA); On-site; USD 181,000 - 194,000; Full time

Job summary

Candel Therapeutics, Inc. is seeking an experienced Clinical Scientist, Associate Director to support oncology development efforts with a focus on prostate cancer and expansion into other solid tumors.

This remote role requires strong data interpretation, medical writing, and regulatory submission capabilities, with occasional travel to Needham, MA as business needs require. You will lead clinical data reviews, support medical monitoring, and collaborate across functions to ensure high-quality

Qualifications

• 5+ years of Clinical Scientist or related clinical development experience in biotech/pharma.
• Oncology clinical development experience required; prostate, lung, brain or solid tumors desirable.
• Hands-on experience with clinical data review and medical monitoring.
• Experience authoring CSRs, Investigator Brochures, protocols, DSURs, IND submissions, and regulatory docs.
• Experience with BLA preparation or regulatory filings is a plus.
• Experience in a small/mid-sized biotech company preferred.

Responsibilities

• Perform ongoing clinical data review and analysis to ensure data integrity and identify trends.
• Support medical monitoring activities including AE reviews and protocol deviations.
• Author and contribute to CSRs, IBs, protocols, ICFs, DSURs, and regulatory submissions.
• Collaborate with Clinical Operations, Regulatory, Biostatistics, Data Management, Medical Writing, and PV.
• Develop study synopses, protocols, SAPs, briefing books, regulatory responses, and publications.
• Review and interpret clinical data to provide insights to study teams.

Skills

Oncology expertise

Clinical data analysis

Medical writing

Regulatory documentation

Collaboration

Project management

Attention to detail

Tools

MedDRA coding

Clinical trial databases

Job description

Candel Therapeutics, Inc. is seeking an experienced Clinical Scientist, Associate Director to support oncology development efforts with a focus on prostate cancer and expansion into other solid tumors.

This remote role requires strong data interpretation, medical writing, and regulatory submission capabilities, with occasional travel to Needham, MA as business needs require. You will lead clinical data reviews, support medical monitoring, and collaborate across functions to ensure high-quality