Neurology Clinical Development Director

Treeline; Watertown (MA); On-site; USD 302,000 - 371,000; Full time

Job summary

Treeline Biosciences seeks a clinician-scientist to bridge basic research with clinical development strategy in a neurology therapeutic portfolio. You will provide strategic medical guidance and lead the design and conduct of development programs aimed at regulatory milestones.

You will create development plans for potential registration trials and stay current with scientific advances. Strong communication, integrity, and GCP adherence are essential in this exempt, on-site role in Watertown, MA.

Qualifications

• MD with Board-certification in neurology and ≥4 years clinical practice.
• Experience leading complex, global early phase clinical programs.
• Familiarity with data analysis, interpretation and clinical relevance.
• Strong communication and collaboration abilities.

Responsibilities

• Provide clinical leadership and strategic medical guidance for neurology therapeutic development.
• Create clinical development plans to support registration trials.
• Maintain up-to-date scientific and clinical knowledge relevant to disease area.
• Liaise with stakeholders, advisory boards, patient groups and regulatory authorities.
• Act as medical monitor and ensure trial data integrity and safety.
• Collaborate across multidisciplinary teams for study analytics and biomarker plans.
• Support regulatory interactions such as end of phase meetings.

Skills

MD with neurology Board-certification

Clinical leadership

Data analysis interpretation

Excellent written and oral skills

Strong interpersonal skills

Good Clinical Practice knowledge

Ethical integrity

Education

MD with Board-certification (Neurology)

PhD preferred

Job description

Treeline Biosciences seeks a clinician-scientist to bridge basic research with clinical development strategy in a neurology therapeutic portfolio. You will provide strategic medical guidance and lead the design and conduct of development programs aimed at regulatory milestones.

You will create development plans for potential registration trials and stay current with scientific advances. Strong communication, integrity, and GCP adherence are essential in this exempt, on-site role in Watertown, MA.