Associate Medical Director, Clinical Development

Blue Earth Diagnostics, Inc. (U.S.); Needham (MA); Hybrid; USD 170,000 - 210,000; Full time

Job summary

Blue Earth Diagnostics, a Bracco Imaging subsidiary, seeks an Associate Medical Director, Clinical Development to lead medical strategy for Phase I–IV radiopharmaceutical trials. The role ensures participant safety, protocol integrity and robust study interpretation within cross-functional teams.

Hybrid work is expected with onsite presence three days a week at 197 First Avenue, Needham, MA; US travel up to 20% may be required.

Qualifications

• MD or equivalent medical degree required with postgraduate training in oncology, radiology, nuclear medicine or pharmaceutical medicine.
• Experience with Phase I–IV clinical development of radiopharmaceuticals and safety monitoring is essential.
• Strong ability to interpret study data and contribute to regulatory submissions and study reports.

Responsibilities

• Provide medical direction for BED-sponsored Phase I–IV global clinical trials of radiopharmaceuticals.
• Develop, review and oversee study documents, safety monitoring, data review plans and regulatory documentation.
• Lead medical data review, safety signals assessment and escalation in line with program timelines.

Skills

Medical monitoring

Clinical trial oversight

Regulatory communications

Cross-functional collaboration

Education

MD or equivalent medical degree

Postgraduate training in oncology/radiology/nuclear medicine

Job description

Blue Earth Diagnostics, a subsidiary of Bracco Imaging, is a global company advancing precision molecular imaging to support timely decisions and better patient outcomes. Founded in 2014, we work closely with clinicians and collaborators, bringing deep expertise to the development and delivery of positron emission tomography (PET) radiopharmaceuticals. Our growing portfolio helps uncover disease sooner and guide treatment choices across multiple disease states, including oncology and cardiology. Backed by a dedicated team, we deliver clear answers when decisions matter most.

Job Purpose:

The Associate Medical Director, Clinical Development provides study-level medical and scientific leadership for assigned Phase I-IV clinical trials of diagnostic radiopharmaceuticals. The role is accountable for the medical integrity, participant safety and clinically robust execution of each study from protocol development through close-out. The Associate Medical Director performs medical monitoring for insourced studies and provides sponsor oversight of outsourced medical monitoring, including the quality and consistency of medical decisions and appropriate escalation. Working within cross-functional study teams, the role leads medical data and safety review, investigator engagement, study-level interpretation and reporting, and contributes to regulatory activities and program strategy under the direction of the Medical Director.

Ideally, this position will operate on a hybrid work schedule, with the expectation of working onsite 3 days a week in our office located at 197 First Avenue, Needham, MA.

Strongly qualified candidates in remote work arrangements within the US may also be considered, and may be required to travel to Needham, MA regularly.

Main Responsibilities, Activities, Duties and Tasks:

• Provide medical direction to BED-sponsored Phase I-IV global clinical development activities for radiopharmaceuticals.
• Develop and review study documents, including protocols, Investigator Brochures, case report forms, medical monitoring and data review plans, clinical study reports and study-level regulatory documentation.
• For insourced studies, act as the sponsor medical monitor. For outsourced studies, define and approve the medical monitoring approach and escalation criteria, oversee the vendor medical monitor and ensure timely, consistent and appropriately documented decisions.
• Provide or oversee participant-level medical decisions relating to eligibility, protocol interpretation, investigator queries, protocol deviations, concomitant medication and safety findings.
• Conduct ongoing medical and safety review, identify emerging trends or potential signals, support pharmacovigilance with individual case and aggregate assessments, and promptly escalation issues that may affect program benefit-risk or participant protection.
• Lead medical data review, clinical query strategy, data review meetings and assessment of medical readiness for database lock.
• Interpret study results and contribute to clinical study reports, regulatory submissions, publications, congress materials and internal development decisions.
• Build effective relationships with investigators, key opinion leaders and sites; support investigator and site identification, feasibility, recruitment, investigator meetings and relevant advisory activities.
• Collaborate with Clinical Operations, Imaging, Biometrics, Pharmacovigilance, Regulatory, Quality, CMC and other functions to identify and resolve study risks, maintain inspection readiness and deliver agreed timelines.
• Provide study-specific medical input to health-authority submissions, responses and meetings, and communicate study status, risks, recommendations and required escalations to the Medical Director.
• Maintain clear study-level medical documentation, capture lessons learned and contribute to development and continuous improvement of relevant SOPs, policies, templates and ways of working.
• Other duties as determined by business needs.

Education

• MD or equivalent medical degree required, with postgraduate clinical training and/or certification in oncology, radiology, nuclear medicine, pharmaceutical medicine or another relevant specialty.
• Current or recent licensure/registration in a recognized jurisdiction (e.g., U.S. state medical board, UK General Medical Council, or EU equivalent).
• A higher research degree or other formal training in clinical research or drug development is desirable
• Able to travel domestically and internationally up to 20% of the time, if required.
• Attendance at conferences, investigator/KOL meetings, and company events may be required.

Professional Experience, Knowledge & Technical Skills

• Clinical (patient care or research) experience beyond that obtained during medical degree
• Working knowledge of the clinical development lifecycle, Good Clinical Practice, protocol design, safety surveillance and pharmacovigilance, medical data review, clinical study reporting and clinical content for IND/CTA and marketing-application documentation.
• Business and market knowledge; pharmaceutical/biotech experience
• Awareness and understanding of good clinical practice in an industry setting
• Experience in supervision of projects and driving time-lines
• Skills in interpretation/evaluation of clinical data.
• Demonstrated record of scientific/medical presentations/publication
• Capable of conducting doctoral level discussions with investigators / collaborators

Why Blue Earth Diagnostics?

We are seeking motivated individuals with drive and determination to succeed in an innovative and respectful team environment. Our employees are empowered to achieve great things and thrive in our exceptionally co-operative culture. As a young and dynamic company experiencing rapid growth, Blue Earth Diagnostics prides itself on providing a clear focus and incentives to achieve our business-critical objectives. We aim to have fun and celebrate each milestone along the way.

If you are seeking a job where you have a clear impact on business success, are working with talented and collaborative colleagues daily, and are doing something great for human healthcare, then this job is for you.

Blue Earth Diagnostics offers a highly competitive salary for high-caliber candidates. We also offer a comprehensive benefits package including a complete healthcare plan, 401k with matching, work/life harmony, and generous paid holidays.

Blue Earth Diagnostics is an equal opportunity employer. All qualified applicants will receive consideration for employment without discrimination on grounds of disability, age, race, color, religion, sex, national origin or any other characteristic protected by law.