
11 - 50 employees
Founded 2017
đ§Ź Biotechnology
đ Pharmaceuticals
âď¸ Healthcare Insurance
Biotechnology ⢠Pharmaceuticals ⢠Healthcare Insurance
Akero Therapeutics is a company pioneering novel therapies to transform the lives of people living with serious metabolic diseases. Their flagship program, Efruxifermin (EFX), is aimed at treating metabolic dysfunction-associated steatohepatitis (MASH) and is currently undergoing multiple clinical trials. Akero is committed to advancing medicine in the field of metabolic diseases and has a strong focus on research, development, and clinical studies.
đ 6 days ago
đ California â Remote
đľ $187k - $279.8k / year
â° Full Time
đ Senior
đ¨ââď¸ Medical Director
Improve your chances of getting an interview by checking your resume score before you apply.

11 - 50 employees
Founded 2017
đ§Ź Biotechnology
đ Pharmaceuticals
âď¸ Healthcare Insurance
Biotechnology ⢠Pharmaceuticals ⢠Healthcare Insurance
Akero Therapeutics is a company pioneering novel therapies to transform the lives of people living with serious metabolic diseases. Their flagship program, Efruxifermin (EFX), is aimed at treating metabolic dysfunction-associated steatohepatitis (MASH) and is currently undergoing multiple clinical trials. Akero is committed to advancing medicine in the field of metabolic diseases and has a strong focus on research, development, and clinical studies.
⢠Serve as a senior thought partner to functional leaders, contributing to program-level planning, risk mitigation, and execution strategies. ⢠Collaborate across Clinical Operations, Biostatistics, Medical, Regulatory, Safety, and Quality to identify and resolve data-related issues impacting timelines, quality, or compliance ⢠Set up data management vendors as required, including authoring of RFPs, reviewing and negotiating data management budgets and contracts ⢠Oversee database status with respect to key performance indicators, metrics, and program level deliverables and timelines to support program timelines ⢠Oversee data review, cleaning, and database lock activities to ensure accuracy and readiness for analysis and regulatory submission ⢠Proactively identify vendor risks, escalate issues as needed, and drive root-cause analysis and corrective actions ⢠Balance quality, timelines, and cost while driving pragmatic solutions aligned with program priorities ⢠Foster a culture of accountability, collaboration, and continuous improvement across internal teams and external partners ⢠Provide direct supervision and periodic review of work for departmental employees, to ensure oversight and execution of clinical development timelines ⢠Direct and mentor a team of data management professionals. ⢠Foster a collaborative environment that encourages innovation and knowledge sharing. ⢠Ensure effective resource allocation and management across research departments. ⢠Drive performance and accountability through clear communication of expectations and goals ⢠Support organizational growth by scaling data management capabilities and processes as the portfolio evolves
⢠Bachelor's degree required; Master's degree in Life Sciences or a related discipline highly preferred. ⢠Minimum of 12 years of experience in clinical development within the pharmaceutical or biotechnology industry, including significant experience as a hands-on clinical data management lead. At least four years of management experience within pharmaceutical development is preferred. ⢠Strong understanding of drug development, FDA regulations, and ICH GCP guidelines, with thorough knowledge of the pharmaceutical industry and the conduct of global clinical studies. ⢠Demonstrated leadership and people-management experience, with a proven track record of leading cross-functional and international teams and influencing senior leaders across functions. ⢠Experience managing clinical data management vendors, contractors, and service providers to ensure delivery of program objectives and timelines. ⢠Strong analytical skills with demonstrated experience gathering, interpreting, and analyzing clinical research and drug development data to support decision-making and risk management. ⢠Excellent communication, presentation, and stakeholder-management skills, with the ability to translate complex data and risks into clear, business-relevant insights. ⢠Understanding of FDA and ICH GCP guidelines to ensure the appropriate conduct of clinical studies required
⢠medical, dental and vision coverage ⢠life insurance ⢠disability insurance ⢠401(k) savings plan ⢠flexible spending accounts ⢠employee assistance program ⢠tuition reimbursement program ⢠voluntary benefits such as group legal ⢠critical illness ⢠identity theft protection ⢠pet insurance ⢠auto/home insurance ⢠time off pursuant to its sick time policy ⢠flexible vacation policy ⢠parental leave policy
Apply Nowđ 6 days ago
Senior Director Medical Monitor ensuring oversight for late-stage clinical trials in asthma and COPD. Working with cross-functional teams to maintain patient safety and protocol compliance in a biopharma setting.
đşđ¸ United States â Remote
đľ $277k - $400k / year
đ° $370M Series B on 2021-11
â° Full Time
đ Senior
đ¨ââď¸ Medical Director
đŚ H1B Visa Sponsor
đ July 9
Associate Director of Medical Information and Communication managing Freenomeâs cancer screening portfolio. Leading medical communications and managing cross-functional partnerships with a focus on scientific and clinical insights.
đşđ¸ United States â Remote
đľ $182.8k - $257.3k / year
đ° $290M Corporate Round on 2022-01
â° Full Time
đ Senior
đ¨ââď¸ Medical Director
đŚ H1B Visa Sponsor
đ July 9
Director for Clinical Trials at Natera, leading innovative clinical services for rare disease and oncology. Engaging in strategic partnerships and managing cross-functional teams to optimize clinical trial outcomes.
đşđ¸ United States â Remote
đľ $169.3k - $211.6k / year
â° Full Time
đ Senior
đ¨ââď¸ Medical Director
đŚ H1B Visa Sponsor
đ July 9
Lead Director providing strategic and operational leadership for Medicaid risk adjustment analytics at CVS Health. Collaborating with teams to ensure compliance and optimize revenue capture.
đşđ¸ United States â Remote
đľ $100k - $231.5k / year
â° Full Time
đ Senior
đ¨ââď¸ Medical Director
đ July 8
10,000+ employees
Executive Director leading Global Medical Affairs Companion Diagnostic program for BeOne. Engaging with cross-functional teams to support successful LPs and ensuring optimal CDx strategy execution.
đşđ¸ United States â Remote
đľ $296.6k - $376.6k / year
â° Full Time
đ Senior
đ¨ââď¸ Medical Director