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Voyager Therapeutics, Inc.
Lexington, MA, United States
About Voyager Therapeutics Voyager Therapeutics, Inc. (Nasdaq: VYGR) is a biotechnology company dedicated to leveraging the power of human genetics to modify the course of - and ultimately cure - neurological diseases. Our pipeline includes programs for Alzheimer's disease, amyotrophic lateral sclerosis (ALS), Parkinson's disease, and multiple oth
Job Source: Voyager Therapeutics, Inc.Voyager Therapeutics, Inc.
Lexington, MA, United States
About Voyager Therapeutics Voyager Therapeutics, Inc. (Nasdaq: VYGR) is a biotechnology company dedicated to leveraging the power of human genetics to modify the course of - and ultimately cure - neurological diseases. Our pipeline includes programs for Alzheimer's disease, amyotrophic lateral sclerosis (ALS), Parkinson's disease, and multiple oth
Job Source: Voyager Therapeutics, Inc.Voyager Therapeutics
Lexington, MA, United States
About Voyager Therapeutics Voyager Therapeutics, Inc. (Nasdaq: VYGR) is a biotechnology company dedicated to leveraging the power of human genetics to modify the course of - and ultimately cure - neurological diseases. Our pipeline includes programs for Alzheimer's disease, amyotrophic lateral sclerosis (ALS), Parkinson's disease, and multiple oth
Job Source: Voyager TherapeuticsRandstad US
Cambridge, MA, United States
category life, physical, and social science occupations reference48363 job details job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to
Job Source: Randstad USAcrivon Therapeutics
Watertown, MA, United States
Acrivon is a clinical stage biopharmaceutical company developing precision oncology medicines that it matches to patients whose tumors are predicted to be sensitive to each specific medicine by utilizing Acrivon’s proprietary proteomics-based patient responder identification platform, Acrivon Predictive Precision Proteomics, or AP3. The AP3 platfor
Job Source: Acrivon TherapeuticsNovo Nordisk A/S
Lexington, MA, United States
The Medical Director serves as the subject matter expert for our products and related data within a Therapeutic Are. The Medical Director is a team player, detail oriented with prior research experience, either in academia or industry. In this role, Medical Director, Director, Clinical Research, Medical, Operations, Monitoring, Manufacturing, Healt
Job Source: Novo Nordisk A/SAVEO Oncology
Boston, MA, United States
Description JOB TITLE: Medical Director, Oncology REPORTS TO: Vice President of Clinical Development DATE PREPARED: May 30, 2024 JOB SUMMARY: AVEO Oncology is seeking a highly skilled and experienced Medical Director to join our dynamic team. The successful candidate will have a strong background in oncology, previous experience in late ph
Job Source: AVEO OncologyNovo Nordisk
Lexington, MA, United States
Novo Nordisk Medical Director Lexington , Massachusetts Apply Now Our Boston Research & Development hub, anchored in the greater Boston area, brings together the best minds in life science innovation. The teams located in facilities in Lexington, Watertown and Cambridge reflect the full R&D continuum, from early research through lat
Job Source: Novo NordiskBoston, MA, United States
JOB TITLE: Medical Director, Oncology
REPORTS TO: Vice President of Clinical Development
DATE PREPARED: May 30, 2024
JOB SUMMARY:
AVEO Oncology is seeking a highly skilled and experienced Medical Director to join our dynamic team. The successful candidate will have a strong background in oncology, previous experience in late phase development strongly preferred; and a proven track record in managing global clinical trials. This role is pivotal in driving the clinical development of our oncology pipeline and ensuring the successful execution of our clinical programs.
PRINCIPAL DUTIES:
Clinical Development Leadership:
Provide medical and scientific leadership in the design, execution, and interpretation of clinical studies.
Collaborate with cross-functional teams, including clinical operations, regulatory affairs, and biostatistics, to ensure alignment on clinical strategy and study design.
Ensure clinical trials are conducted in compliance with applicable regulations, guidelines, and company policies.
Global Clinical Trial Management:
Oversee and manage global clinical studies, ensuring consistency and quality across all regions.
Lead interactions with global regulatory agencies and key opinion leaders to facilitate clinical trial approvals and align on clinical development plans.
Monitor study progress and address any issues that arise to ensure timely completion and high-quality data.
Medical Monitoring and Safety Oversight:
Serve as the medical monitor for assigned clinical trials, providing ongoing medical oversight and guidance.
Assess and interpret clinical trial data, ensuring accuracy and completeness of safety and efficacy information.
Collaborate with pharmacovigilance teams to monitor and manage adverse events and other safety concerns.
Data Analysis and Reporting:
Participate in data analysis, interpretation, and presentation of clinical study results to internal and external stakeholders.
Contribute to the preparation of clinical study reports, regulatory submissions, and scientific publications.
Present clinical data at scientific conferences and advisory boards.
Stakeholder Engagement:
Develop and maintain strong relationships with key opinion leaders, investigators, and clinical trial sites.
Act as a key point of contact for external partners, including regulatory authorities, academic institutions, and industry collaborators.
Represent AVEO Oncology at scientific meetings, conferences, and industry events.
REQUIRED QUALIFICATIONS/EXPERIENCE (BASIC QUALIFICATIONS):
Education:
Medical Doctor (MD) degree is required.
Experience:
Minimum of 3-5 years of experience in oncology clinical development, familiarity with late phase clinical studies is required.
Demonstrated experience in managing global clinical trials and navigating international regulatory environments.
Skills:
Strong clinical and scientific acumen in oncology.
Excellent leadership, communication, and interpersonal skills.
Proven ability to work effectively in a cross-functional, global team environment.
Strong analytical and problem-solving skills with a keen attention to detail.
Preferred Qualifications:
Experience working within a biotechnology or pharmaceutical company.
Demonstrated ability to drive clinical development strategies and make data-driven decisions.
Prior experience interacting with global regulatory agencies and key opinion leaders.
Experience in head and neck oncology clinical trials.
About AVEO
AVEO is a commercial-stage, oncology-focused biopharmaceutical company committed to delivering medicines that provide a better life for patients with cancer. AVEO currently markets FOTIVDA (tivozanib) in the U.S. for the treatment of adult patients with relapsed or refractory renal cell carcinoma (RCC) following two or more prior systemic therapies. AVEO continues to develop FOTIVDA in immuno-oncology combinations in RCC and other indications and has several other investigational programs in clinical development. AVEO is committed to creating an environment of diversity, equity and inclusion to diversify representation within the Company.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Email Alert for Medical Director jobs in Boston, MA, United States
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