Email Alert for
ⓘ There was an unexpected error processing your request.
Please refresh the page and try again.
If the problem persists, please contact us with your issue.
You can always manage your preferences and update your interests to ensure you receive the most relevant opportunities.
Get ready to discover your next great opportunity.
Editas Medicine
Cambridge, MA, United States
At Editas, we're driven by a collective purpose, to bring transformative and life changing therapies to people living with serious diseases with the greatest unmet needs. This fuels our drive to excel in scientific innovation, allowing us to harness the power and potential of CRISPR/Cas9 and CRISPR/Cpf1 (Cas12a) gene editing. We believe our people
Job Source: Editas MedicineEditas Medicine
Cambridge, MA, United States
At Editas, we're driven by a collective purpose, to bring transformative and life changing therapies to people living with serious diseases with the greatest unmet needs. This fuels our drive to excel in scientific innovation, allowing us to harness the power and potential of CRISPR/Cas9 and CRISPR/Cpf1 (Cas12a) gene editing. We believe our people
Job Source: Editas MedicineSalioGen Therapeutics
Lexington, MA, United States
About Us: At SalioGen, we are leveraging the intrinsic genome engineering features of human evolution to harness the power of genetic medicine. Our approach, which we call "Gene Coding", is guided by our Exact DNA Integration Technology (EDIT): a genome engineering platform using the proprietary mammal-derived enzyme saliogase. With broad applicabi
Job Source: SalioGen TherapeuticsConfidential
Boston, MA, United States
Vice President, Clinical Development About the Company Rapidly-growing life sciences & biotechnology organization Industry Biotechnology Type Public Company Founded 2010 Employees 10,001+ Categories B2B SAAS Biotechnology Health Care Life Science Medical Healthcare Pharmaceuticals Medical Care International Trade Therapeutics Medicines Precision E
Job Source: ConfidentialXilio Therapeutics
Waltham, MA, United States
Xilio Therapeutics is a clinical-stage biotechnology company discovering and developing tumor-activated immuno-oncology (I-O) therapies with the goal of significantly improving outcomes for people living with cancer without the systemic side effects of current I-O treatments. The company is using its proprietary platform to advance a pipeline of no
Job Source: Xilio TherapeuticsConfidential
Waltham, MA, United States
Vice President, Clinical Development About the Company Innovative biopharmaceutical company developing tumor-selective immunotherapies Industry Pharmaceuticals Type Privately Held Founded 2016 Employees 51-200 Categories Pharmaceuticals Medicine Manufacturing Chemical Products Biotechnology About the Role The Company is seeking a Vice President,
Job Source: ConfidentialXilio Therapeutics
Watertown, MA, United States
Vice President, Clinical Development Xilio Therapeutics is a clinical-stage biotechnology company discovering and developing tumor-activated immuno-oncology (I-O) therapies with the goal of significantly improving outcomes for people living with cancer without the systemic side effects of current I-O treatments. The company is using its proprietar
Job Source: Xilio TherapeuticsXilio Therapeutics
Watertown, MA, United States
Vice President, Clinical Development Xilio Therapeutics is a clinical-stage biotechnology company discovering and developing tumor-activated immuno-oncology (I-O) therapies with the goal of significantly improving outcomes for people living with cancer without the systemic side effects of current I-O treatments. The company is using its proprietar
Job Source: Xilio TherapeuticsBoston, MA, United States
Our client is a precision oncology pharmaceutical company. They have asked us to assist them in their search for a Vice President, Clinical Development.
Major tasks and responsibilities include:
Provides strategic medical input into the development of the company's key assets identifying relevant target patient populations.
Leads Product Development Teams and contributes to the creation of a successful lifecycle management strategy.
Collaborates with physicians, scientists, regulatory professionals, biostatisticians, regulatory, executive staff, and others as necessary to validate and design clinical development plans including individual clinical trial protocols.
Collaborates with Clinical Operations to execute clinical trials from beginning to end, overseeing study conduct, and interpreting the study results consistent with objectives to define safety, efficacy, pharmacokinetic/pharmacodynamic, patient reported outcomes, and application of data to a targeted patient population.
Acts as Medical Lead and overseesmedical monitoring activities.
Leads the Product Safety Sub-Team.
Acts as primary medical contact for study physicians and sites engaging during study feasibility through close-out.
Provides input into and reviews other relevant study documents.
Acts as subject matter expert on clinical and medical strategic initiatives and provide internal training/ collaboration as needed.
Interprets clinical study and safety data for relevant clinical and regulatory documents.
Develops and maintains strong, collaborative relationships with key internal and external stakeholders.
Collaborates with Principal Investigators in the evaluation and assessment of emerging clinical experiences, data centric publications, and communication of emerging clinical data.
Networks extensively to develop long-term strategic partnerships with thought leaders both internally and externally, in support of the company's vision.
We seek candidates with the following qualifications: An MD or equivalent with board certification or board qualifications in medical or pediatric or radiation oncology is required.
Must have 10+ years of relevant experience, including medical training and clinic experience.
Requires a minimum of 3 years drug development experience in Pharma, Biotech or CRO in Oncology drug development supporting studies to develop new biological therapeutics.
Clinical experience in the implementation and development of companion diagnostics is desired.
Must have a strong working knowledge of the clinical drug development process. Requires a track record in the conduct/participation in clinical trials (investigator initiated, company sponsored or cooperative group trials) and their subsequent publications.
Successful academic research publication history or history of medical practice is required.
The demonstrated ability to function in a matrix organizational environment is required.
Must have solid personal and professional relationships with key opinion leaders (KOLs) in the oncology therapeutic community. Must have strong credibility within the broader US/European medical community which includes the ability to reach out to key thought leaders in academia.
US State Licensure to practice medicine is desirable.
Must be able to travel as necessary (up to 20%).
If interested, please apply directly to this job posting. No calls please. Include your daytime phone number and we will contact you confidentially or reply to your email.
Fairway Consulting Group is included in Hunt Scanlon's list of Top 50 Healthcare & Life Sciences Search Firms and Forbes' list of Top 200 Best Executive Recruiting Firms .
#J-18808-Ljbffr
Email Alert for Vice President, Clinical Development jobs in Boston, MA, United States
ⓘ There was an unexpected error processing your request.
Please refresh the page and try again.
If the problem persists, please contact us with your issue.
You can always manage your preferences and update your interests to ensure you receive the most relevant opportunities.
Get ready to discover your next great opportunity.