Clinical Development Medical Lead (Associate MD)

Blue Earth Diagnostics Inc.; Needham (MA); On-site; USD 150,000 - 175,000; Full time

Benefits offered by this job

Healthcare plan

401k with matching

Work-life harmony

Generous paid holidays

Job summary

Blue Earth Diagnostics Inc. seeks an Associate Medical Director to lead medical and scientific activities for Phase I–IV diagnostic radiopharmaceutical trials.

You will oversee medical monitoring, data review, and investigator engagement to ensure safety and robust study interpretation. Collaborating with Clinical Operations, Regulatory, and other functions, you will contribute to regulatory submissions, publications and development decisions under the Medical Director.

Qualifications

• MD or equivalent medical degree with postgraduate clinical training or specialty certification.
• Experience in clinical development lifecycle, pharmacovigilance and safety review.
• Supervision of projects and timelines in a pharmaceutical/biotech setting.

Responsibilities

• Provide study-level medical and scientific leadership for Phase I–IV trials of diagnostic radiopharmaceuticals.
• Lead medical data review, safety assessment, and regulatory documentation.
• Collaborate with cross-functional teams to ensure compliant, timely study delivery.
• Support health-authority submissions and program strategy under the Medical Director.

Skills

Clinical trial experience

Medical monitoring

Data review & safety

Regulatory submissions

Education

MD or equivalent first medical degree

Postgraduate clinical training/certification in oncology/radiology/nuclear medicine/pharma medicine

Job description

Blue Earth Diagnostics Inc. seeks an Associate Medical Director to lead medical and scientific activities for Phase I–IV diagnostic radiopharmaceutical trials.

You will oversee medical monitoring, data review, and investigator engagement to ensure safety and robust study interpretation. Collaborating with Clinical Operations, Regulatory, and other functions, you will contribute to regulatory submissions, publications and development decisions under the Medical Director.