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Treeline · 1 day ago

Medical Director

Watertown, Massachusetts, United States

Full-time

Onsite

Lead/Staff, Director/Executive

$302K/yr - $371K/yr

4+ years exp

Treeline Biosciences is focused on developing new hematology and oncology agents, and they are seeking a Medical Director to provide strategic medical guidance. The role involves leading clinical development programs, ensuring compliance with regulations, and collaborating with multidisciplinary teams to support clinical trial execution.

BiotechnologyHealth CareLife ScienceMedicalPrecision Medicine

Responsibilities

Provides clinical leadership and strategic medical guidance for the development of new agents across the company’s early pipeline

Responsible for creating clinical development plan(s) that foresee and support subsequent registration trials

Maintains the highest standards of scientific and clinical knowledge in the specific therapeutic area(s) of assignment

Stays informed and up to date of internal and external developments, trends, and other dynamics relevant to the clinical development plan, and maintains a current view of the relevant disease area(s) to inform strategy

Liaises with internal stakeholders and outside experts, advisory boards, patient advocacy groups and regulatory authorities and represent assigned programs to those groups and authorities

May support Business Development and Licensing activities

Collaborates with clinical scientists, clinical operations, scientists and subject matter experts to develop clinical trial protocols

Provides the clinical and expert input in the development of clinical sections of Investigator Brochures, presentations, and other materials

Regularly engages with the relevant external investigators; participate in the identification and selection of appropriate external investigators and sites

Applies their medical knowledge to guide the safe, ethical and efficient conduct of the trials under their responsibility

Maintains compliance with Good Clinical Practice guidelines and Treeline Standard Operating Procedures

Acts as the medical monitor for assigned studies and conduct ongoing reviews of clinical trial data

Collaborates within a multidisciplinary team including biostatisticians, data managers and statistical programmers to develop study analytics and data review plans

Collaborates with the Translational Biomarker team to strategize, design, and implement biomarker plans

Reviews study data to ensure correct medical/scientific data interpretation for interim and final study reporting

Collaborates with Clinical Operations for site selection, feasibility, and query resolution etc

Collaborates with relevant team members to support regulatory interactions such as end of phase meetings

Qualification

MD with Board-certificationClinical practice experienceExperience leading oncology programsData analysis techniquesClinical Practice knowledgeEthical integrityCommunication skillsInterpersonal skills

Required

MD with Board-certification (or equivalent expertise) in a Heme/Onc sub-specialty

Clinical practice experience ≥ 4 years

Additional lab-based science training is required

Experience leading complex, global, early phase, oncology clinical programs from the pharma/biotech industry and/or credible experience from an academic medical center

Experience working with the principles and techniques of data analysis, interpretation, and clinical relevance

Excellent communication skills, written and oral

Strong interpersonal skills

Thorough knowledge of Good Clinical Practice

Impeccable personal ethical integrity and a commitment to improving the outcomes for patients