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Temporary 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 / 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 ...

Job Post Title 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 ...

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Temporary Chief Medical Officer Biotech information

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$92K

$274.6K

$399K

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

As of Aug 9, 2026, the average yearly pay for temporary 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 is the difference between Temporary Chief Medical Officer Biotech vs Medical Science Liaison?

AspectTemporary Chief Medical Officer BiotechMedical Science Liaison
CredentialsMedical degree, board certification, industry experienceMedical or scientific degree, advanced degrees preferred
Work EnvironmentExecutive leadership, strategic planning, cross-functional teamsScientific communication, peer engagement, education
Employer & Industry UsageBiotech companies, pharmaceutical firms, clinical developmentPharmaceutical companies, biotech firms, medical device companies

The Temporary Chief Medical Officer Biotech focuses on strategic leadership, clinical oversight, and regulatory compliance at an executive level, often overseeing multiple projects. In contrast, a Medical Science Liaison primarily engages in scientific communication, educating healthcare professionals, and supporting product development. While both roles require medical or scientific credentials, the CMO role is more strategic and leadership-oriented, whereas the MSL role emphasizes scientific expertise and peer engagement.

What cities are hiring for Temporary Chief Medical Officer Biotech jobs? Cities with the most Temporary Chief Medical Officer Biotech job openings:
What are the most commonly searched types of Chief Medical Officer Biotech jobs? The most popular types of Chief Medical Officer Biotech jobs are:
What states have the most Temporary Chief Medical Officer Biotech jobs? States with the most job openings for Temporary Chief Medical Officer Biotech jobs include:

Chief Medical Officer

Clinical Dynamix, Inc.

Jersey City, NJ

Full-time

Re-posted 8 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)