Medical Director Salary at Empowerdx BETA

SciPro is partnered with an exciting clinical stage ADC focused oncology biotech to hire a Senior Medical Director for their team. This role would report into the Chief Medical Officer, and would be focused on early phase clinical trials. Key Responsibilities -Design and execution of clinical development plans -Responsible for medical monitoring of key studies -Provide medical input for protocols, IBs, CSRs, regulatory responses and submissions -Interface with other key leaders and team members within the company Qualifications: -MD or MD/PhD -Industry clinical development experience -Experience in phase I and II studies preferred -Ability to interface with and provide oversight over the cross-functional clinical team -Solid tumor oncology expertise

Canopy Life Sciences is a well-respected vendor & partner in the life sciences industry, assisting pharmaceutical and life sciences clients in various functional areas of expertise. Our culture is one of empowerment. Everyone has a voice and plays a role in the success of the business and a role in developing our values & behaviors. We recruit, train, and develop people to ensure the very best for our client partners. Position Summary - Senior Medical Director The Senior Medical Director is responsible for medical and clinical development activities for a pharmaceutical company's portfolio focused on Hepatology from Phase 3 planning through product approval and post-approval life cycle management. This individual will oversee both day-to-day medical monitoring activities and strategic protocol development and management. The role requires strong communication and leadership skills, along with extensive experience in drug development. Key Responsibilities: Collaborate with the leadershi

Executive Medical Director Clinical Development Greater Boston Area - Hybrid Compensation: $250,000-290,000 + 25% bonus + Lucrative RSU package Company Summary: We have partnered with a mid-sized biotech company at the forefront of developing innovative therapeutic products for endocrine and orphan lung diseases. They already have two key products approved that generated over $200 million in revenue this past year and the have 2 phase 3 studies in development. One of their drugs in development has fast-track designation and given their previous track record of getting pulmonary products approved you can have additional confidence in the efficacy of their science. Their unique delivery method can be used with a variety of drugs, including small molecules and biologics, making it a versatile platform for different therapeutic applications for years to come. If interested in learning more don't hesitate to apply. Primary Responsibilities: Study Execution: Conduct clinical trials in compli

Job Title: Senior Medical Director - Oncology Location: Cambridge, MA Employment Type: Full-time About Our Client: Our client is a leading biopharmaceutical company focused on pioneering innovative therapies to address unmet needs in oncology. Their mission is to transform the treatment landscape through cutting-edge research and clinical advancements. They are seeking a highly experienced and dynamic individual to join their team as the Senior Medical Director - Oncology. Position Overview: The Senior Medical Director will play a pivotal leadership role in the strategic direction and execution of oncology clinical trials. With over 20 years of experience in clinical development, including a deep background in oncology and IND submission, this position requires a seasoned leader to drive the development of novel therapies through clinical phases while ensuring alignment with regulatory standards and organizational goals. Key Responsibilities: Lead and oversee the clinical development s

Senior Medical Director, Drug Safety & Pharmacovigilance The Senior Medical Director (Sr. MD) will serve as a Product Safety Lead for clinical development programs and/or post-marketing products. Reporting to the VP of Drug Safety and Pharmacovigilance, this role involves leading medical assessment and interpretation of safety data from clinical trials, post-marketing reports, aggregate reports, and literature. The Sr. MD will collaborate cross-functionally to support clinical programs, regulatory filings, and global safety activities. Key Responsibilities: Provide medical safety leadership in clinical studies, including strategic safety monitoring and signal detection. Collaborate with Clinical and other teams on trial protocols, informed consent forms, investigator brochures, and safety information. Contribute to aggregate safety reports, study reports, and risk management plans. Support development and updates of standard operating procedures and safety guidance documents. Act as a

Medical Director, Immuno-Oncology We are a clinical-stage biopharmaceutical company developing next-generation multispecific antibodies and vaccines for cancer and infectious diseases. Our innovative antibody platforms combine multiple biologic components into a single molecule, offering greater versatility and potency against complex diseases than traditional approaches. Our pipeline includes candidates targeting both solid and hematological tumors, as well as several of the world's most pressing viral threats. Our leadership team consists of globally recognized medical innovators with a strong track record of delivering breakthroughs for patients. Position Overview The Medical Director will be a key member of the program and clinical development teams, playing a pivotal role in shaping and executing clinical strategies for immuno-oncology programs. This role requires strong medical judgment, collaboration, leadership, and communication skills, along with a deep understanding of clini

At MannKind our employees are our number one asset, and we continue to be a tight-knit community where each of us has a critical role in our success. Committed to diversity, at MannKind we depend on a rich blend of ideas, backgrounds, and working styles in our quest to change the world for the better. About MannKind MannKind Corporation focuses on the development and commercialization of innovative inhaled therapeutic products and devices to address serious unmet medical needs for those living with endocrine and orphan lung diseases. We are committed to using our formulation capabilities and device engineering prowess to lessen the burden of diseases such as diabetes, nontuberculous mycobacterial (NTM) lung disease, pulmonary fibrosis, and pulmonary hypertension. Our signature technologies - dry-powder formulations and inhalation devices - offer rapid and convenient delivery of medicines to the deep lung where they can exert an effect locally or enter the systemic circulation, dependin

1. Serves as the primary physician for reporting to the Food and Drug Administration and in such capacity provides medical oversight in compliance with applicable Federal and State regulations including the applicable sections of Title 21 of the Code of Federal Regulations and monitors medical compliance of the center. 2. Either serves as or delegates to another appropriate physician the duties of "laboratory director", "technical consultant", or "clinical consultant" as prescribed by the Clinical Laboratory Improvement Act of 1988 regulations (CLIA). Assures that CLIA/COLA training, CLIA/COLA proficiency testing for hematocrit and total protein, and signed of logs involving standardization takes place. 3. Reviews, understands, and complies with all CSL Plasma Services policies and procedures in the performance of services. Maintains high medical standards and ensures that cGMPs are adhered to through involvement with center management, center quality unit, and overall center activitie