Medical Director Salary at Old Colony Hospice Inc BETA

Overview We are seeking an innovative physician-scientist with expertise in Clinical Research, focusing on the Cardiovascular therapeutic area. This role involves early clinical development, including target nomination, collaboration with Research teams, and driving translational research and biomarker strategies. You will provide clinical leadership, linking Research, Clinical Development, and Commercial teams, and help shape the strategy for the Cardiovascular Therapeutic Area. The role also involves guiding clinical development decisions, advising on novel targets, and collaborating with external experts. While focused on cardiovascular therapeutics, there may be opportunities to work in other areas. Key Responsibilities Lead strategically, offering a science and data-driven clinical research perspective for early-stage projects and programs. Provide expert guidance to the Research team on decisions with significant clinical implications. Contribute clinical research insights (e.g.,

Location: Waltham, MA (Hybrid) Job Overview: Seeking a Clinical Development Professional to strategize, plan, and manage clinical activities for cancer immunotherapy development in a dynamic, team-oriented environment. Primary Job Responsibilities: Design early-phase clinical trials for novel cancer treatments, write trial documents. Assist with clinical site selection and train trial personnel for study success. Monitor trials, analyze data, and contribute to publications and regulatory meetings. Build partnerships with academic, pharmaceutical, and patient advocacy groups. Ensure ethical compliance and maintain disease expertise to support strategic efforts. Primary Job Requirements: MD/PhD in hematology / oncology with 3-5 years as Oncology Medical Director in pharma/biotech, extensive experience in IO drug development to market in the US/EU. Expert in clinical trial design, regulatory standards, and can independently support complex research with minimal direction. Dual clinical an

Title: Senior Director Medical and Safety Reporting Relationship: This position will report to the Senior Vice President, Clinical Development Compensation: Market Salary + 25% Bonus Location: Boston, MA / New England - Must AT LEAST be able to come onsite 1 week per month for Team Week. Position Overview: Under the supervision of the SVP Clinical Development/CMO the Senior Director Medical and Safety will perform a key role in the continuing clinical development in collaboration with his/her cross functional colleagues and be accountable for implementing and managing all pharmacovigilance related activities and support clinical development activities. The Senior Director Medical and Safety will also monitor and document safety data to identify trends and potential safety signals/issues within and across all clinical studies and populations. As part of the execution of strategy, he/she will work closely with Regulatory, Clinical Operations, Biostatistics and external vendors responsibl

Position: Senior Medical Director, Medical Affairs Strategy Location: Boston, MA (Hybrid – 3 days onsite) Length: 6+ months Job Description: Our client is seeking a dynamic and experienced Senior Medical Director to join a global leader in the biotechnology industry. This key position is part of the Medical Affairs Strategy group and will focus on a cutting-edge therapeutic area in hematology. The successful candidate will take charge of the execution of medical strategies for an innovative gene-editing therapy, driving its clinical and commercial success. If you are a results-oriented physician with deep expertise in hematology and a passion for advancing patient care, we encourage you to apply. Essential Duties and Responsibilities (but not limited to): Develop and implement comprehensive medical affairs plans, including launch and life cycle management strategies. Interpret scientific and clinical data to assess its potential impact on clinical practice and guide disease management

Dewpoint Therapeutics is building a highly collaborative team to harness the power of biomolecular condensates. Together, we are leveraging a transformative shift in the understanding of cellular biology to discover and advance breakthrough therapeutics for the toughest diseases. As a growing organization, we are hands-on, agile, and relentlessly focused on innovation and execution. We’re seeking a Senior Medical Director who thrives in a role where they can roll up their sleeves, shape strategies, and take charge of delivering on clinical development initiatives. This is an opportunity for a skilled and action-oriented individual to lead from the front, actively driving the design, execution, and management of clinical trials while building and refining our clinical development strategies. If you’re ready to immerse yourself in the details, execute with precision, and collaborate to move programs forward efficiently, we want to hear from you! In this position, you’ll be part of an ene

Location: Cambridge, MA (Hybrid) Focus: Oncology Job Overview: Seeking a dynamic Medical Director to oversee clinical trials, including design, operational feasibility, safety monitoring, and study close-out activities, while collaborating with various experts and teams in a fast-paced environment. Primary Job Responsibilities: Author clinical documents and provide clear trial results summaries for publications and regulatory purposes. Oversee drug safety and ensure ethical conduct in clinical trials. Facilitate site initiation visits and nurture stakeholder relationships for strategic alignment. Incorporate new scientific insights into development plans and streamline data review and monitoring processes. Primary Job Requirements: MD, MD/PhD, or an advanced degree with over 5 years of experience in clinical development, specifically in early-stage oncology trials globally. Expertise in designing clinical trials, including protocols and statistical analysis. Strong experience with clin

Key Duties and Responsibilities: Develops medical affairs plans, including Launch and Life Cycle Management plans Critically interprets scientific data, determines the potential impact of new research on clinical practice, and uses scientific and clinical data to formulate frameworks and disease management approaches Provides input from medical community into clinical development and commercial strategies Effectively communicates scientific data through presentations and publications Ensures country/regional insights and needs are considered in global medical strategies and activities Provides scientific input and expertise as a medical reviewer and supports the development of global medical, commercial, regulatory, and reimbursement documents Performs/oversees medical/scientific training for Medical, Commercial, and other internal stakeholders Reviews investigator-sponsored study (ISS) proposals and other research grants Knowledge and Skills: Deep understanding of global medical, regu

I am working with an exciting commercial-stage client who are looking for an MD to join their rapidly expanding team, to take on the role of Senior Medical Director, Global Drug Safety (MD). This is an onsite role where you will be expected to be in office in MA at least 3 days per week. For background, the company works across immunology and oncology in a number of modalities. Due to program demands and expanding pipeline, the VP of Global Drug Safety is looking to hire 1x physician as oncology compound lead (Senior Director) to lead safety across select oncology trials in early development. Culture fit is critical to my client. Current team members are experts in their field and high performing. Therefore, you should be a team player, who is adaptable, who can pivot on plan and remain flexible to the needs of the program you are working on. You should be able to think with first principles, with no task being too small, and excited about the journey you have the opportunity to be a p