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Chief Medical Officer Biotech Jobs (NOW HIRING)

CHIEF MEDICAL OFFICER Apply now Job No: 541031 Work Type: Full-time Location: PHOENIX Categories: Executive/Management, Healthcare/Medical Professional Level, Health and Nutrition Services ARIZONA ...

Chief Medical Officer (CMO) Southwest Care Center is seeking an experienced, collaborative physician leader to serve as our Chief Medical Officer (CMO). This executive leadership role combines ...

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Chief Medical Officer / Physician Department: Medical Reports To: Chief Executive Officer Schedule: Monday-Friday, 8:00 a.m.-5:00 p.m. Position Summary The Chief Medical Officer / Physician provides ...

Physician Job Post Summary Seeking a Chief Medical Officer (CMO) in Spokane, WA to provide strategic clinical leadership, oversee provider supervision and quality initiatives, mentor medical staff ...

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$92K

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How much do chief medical officer biotech jobs pay per year?

As of Aug 8, 2026, the average yearly pay for chief medical officer biotech in the United States is $274,592.00, according to ZipRecruiter salary data. Most workers in this role earn between $237,000.00 and $327,500.00 per year, depending on experience, location, and employer.

What are the most common challenges faced by a chief medical officer in a biotech company?

Chief Medical Officers in biotech often face the challenge of balancing rigorous scientific standards with accelerated development timelines, particularly in a fast-evolving regulatory landscape. They must navigate complex stakeholder relationships, including collaborations with R&D, regulatory authorities, and external partners, all while ensuring patient safety and compliance. Additionally, CMOs frequently oversee multiple clinical programs simultaneously, requiring strong prioritization and resource allocation skills. Success in the role often depends on effectively communicating scientific vision and aligning cross-functional teams with organizational goals.

What is a chief medical officer biotech?

A Chief Medical Officer (CMO) in biotech is a senior executive responsible for overseeing the medical and clinical strategy of a biotechnology company. They lead clinical development programs, regulatory strategy, and medical affairs to ensure the safety and efficacy of new therapies. The CMO collaborates with research teams, regulatory agencies, and commercial departments to bring innovative treatments to market. Their role is crucial in guiding a company's scientific vision and ensuring compliance with healthcare regulations.

What are the key skills and qualifications needed to thrive as a chief medical officer biotech, and why are they important?

To thrive as a Chief Medical Officer in biotech, you need extensive clinical expertise, a deep understanding of drug development, board certification (often in a relevant specialty), and significant leadership experience. Familiarity with regulatory frameworks (FDA, EMA), clinical trial management systems, and compliance software is crucial, as is experience guiding product development. Outstanding communication, strategic vision, and the ability to lead cross-functional teams are highly valued soft skills. These capabilities ensure successful translation of scientific advances into safe, effective biotechnological products while maintaining regulatory compliance and driving the organization's mission.

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Infographic showing various Chief Medical Officer Biotech job openings in the United States as of August 2026, with employment types broken down into 92% Full Time, and 8% Part Time. Highlights an 77% In-person, and 23% Remote job distribution, with an average salary of $274,592 per year, or $132 per hour.

Chief Medical Officer

Clinical Dynamix, Inc.

Jersey City, NJ

Full-time

Re-posted 7 days ago


Job description

Chief Medical Officer

POSITION SUMMARY

The Chief Medical Officer is a strategic partner to the Chief Executive Officer, helps build, develop, lead and drive the Company’s preclinical through clinical pipeline. This leader is responsible for the company’s drug development portfolio including responsibility for prioritizing and accelerating the development of Company’s drug candidates. The CMO serves as the key member of the Executive Team and actively participates in strategic planning, partnering discussions and presentations to the Board of Directors and investors.

Key Responsibilities

Areas of specific responsibility and attention will include the following:

· Provide leadership and clinical perspective to the research, development, quality and comprehensive regulatory strategies.

· Manage the overall clinical development for lead programs including early development, clinical proof of concept, pivotal studies and regulatory submissions.

· Ensure Company meets its clinical and regulatory milestones.

· Represent Company at the highest level at the FDA, EMEA and other regulatory agencies.

· Maintain understanding of competitors and clinical developments in relevant therapeutic areas by attending scientific meetings and tracking literature.

· Represent and manage the company’s clinical and regulatory programs to diverse audiences including: FDA, shareholders, corporate partners, Board of Directors and other key stakeholders.

· Represent Company both internally and externally vis-à-vis the scientific and business communities including scientific conferences, presentations, industry and Wall Street.

· Build and maintain solid working relationships with key opinion leaders and lead clinical investigators. Establish and foster relationships with the international scientific and medical community.

· Actively assist in seeking product and/or technology alliances with appropriate pharmaceutical company partners to enhance/expedite the development of the company’s assets.

· Helping to establish and maintain collaborations with partners in academia, government and industry.

PROFESSIONAL Experience/QUALIFICATIONS

The successful candidate must have extensive senior-level experience in clinical development, ideally with both larger pharmaceutical as well as with biotechnology companies. This person will have a thorough understanding of all the requirements and processes needed to take a potential drug through clinical development and ultimately registration.

Key requirements will include:

· An MD or MD/PhD with strong leadership skills and proven biopharmaceutical industry experience in leading clinical development of therapeutic programs, specifically in the Nephrology space is essential.

· Strong leadership skills and proven biopharmaceutical industry experience in leading clinical development from preclinical to phase 3 therapeutic programs. A record of accomplishment including developing, planning, designing and implementing clinical studies in the Nephrology space and experience with the successful registration of therapeutics is highly desirable.

· Experience with IND and NDA submissions including formal interaction with regulatory agencies is essential.

· A thorough understanding of the drug development process.

· Entrepreneurial, resourceful, strategic and energetic leader who is an assertive, driven and hands-on individual with unquestionable integrity.

· Credibility within the international medical and scientific community. Solid personal and professional relationships with key opinion leaders in the nephrology field is desirable.

· Excellent interpersonal and communication skills with ability to relate to both internal and external stakeholders. Ability to develop strong positive relationship with senior management and Board of Directors and provide leadership and guidance to a high functioning development team.

· Experience presenting to a wide variety of audiences including internal teams, Board of Directors, investors, medical and scientific communities.

· Highly developed understanding of the external market place to identify long-term benefits for unmet patients’ and customers’ needs.

· Strong management skills and a good reputation for managing others to succeed.

EDUCATION

An MD or MD/PhD is required. (Nephrology / Internal Medicine)