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Medical Advisor Medical Monitor Jobs (NOW HIRING)

Novotech

Medical Scientific Advisor

Brooklyn, CT · On-site

The Medical Advisor is a senior scientific and medical expert responsible for providing strategic ... Support medical monitoring and safety-related discussions when required. * Mentor teams and ...

Crisis24

Nurse Advisor - Medical Assistance

Annapolis, MD · On-site

$90K - $95K/yr

The (Medical Assistance) Nurse Advisor is critical in supporting the Medical Operations - Medical Team department and is integral to the provision of Medical Assistance. * Our role is to review ...

Eli Lilly and Company

Advisor - Medical Physics

The Advisor - Medical Physicist will provide hands-on technical expertise in SPECT image reconstruction (required), dosimetry analysis, scanner calibration, tool development, validation, QC workflows ...

United Therapeutics Corporation

Minimum Requirements MD, DO or Foreign Equivalent ie MBBS 7+ years of relevant experience, including either: (1) 7+ years of experience as a Medical Monitor in pharmaceutical product development ...

UCB

Medical Strategy Lead Clinical Advisor

Atlanta, GA · On-site +1

$213K - $280K/yr

... Advisor to join our Medical Neurology, Epilepsy & Rare Syndromes team, preferably based in our ... Monitor scientific advances and competitive developments in epilepsy and neurology. * Provide ...

New

Truist

Medical Wealth Advisor

Philadelphia, PA · On-site

... medical markets via event attendance. 9. Participate in campaigns or volunteer at committee level within non-profits in local market. 10. Support Wealth Advisor teammates through collaborative ...

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Medical Advisor Medical Monitor information

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How much do medical advisor medical monitor jobs pay per hour?

As of Sep 15, 2026, the average hourly pay for medical advisor medical monitor in the United States is $53.85, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $78.37 per hour, depending on experience, location, and employer.

What is a medical advisor medical monitor?

Medical Advisor Medical Monitors are healthcare professionals who oversee the safety and scientific integrity of clinical trials. They are responsible for monitoring patient safety, evaluating adverse events, and ensuring that studies comply with regulatory requirements and ethical standards. Their role bridges clinical practice and research, providing medical expertise to study teams and helping to interpret clinical data. They also act as a key point of contact between sponsors, investigators, and regulatory authorities throughout the trial process.

How does a medical advisor medical monitor typically collaborate with clinical research teams during a trial?

A Medical Advisor Medical Monitor works closely with clinical research teams by providing medical oversight throughout the course of a clinical trial. They review safety data, address medical queries from investigators, and ensure the study protocol is adhered to from a medical perspective. Regular meetings with data management, regulatory, and pharmacovigilance colleagues are common to discuss patient safety, protocol deviations, and emerging data. This role requires excellent communication skills as they bridge clinical, regulatory, and operational teams to ensure participant safety and trial integrity.

What are the key skills and qualifications needed to thrive as a medical advisor medical monitor, and why are they important?

To thrive as a Medical Advisor Medical Monitor, you need a strong medical background (such as an MD or PharmD), clinical research experience, and deep knowledge of therapeutic areas relevant to the trials. Familiarity with clinical trial management systems (CTMS), medical safety databases, and regulatory guidelines like GCP and ICH is essential, and certifications in clinical research can be advantageous. Excellent communication, critical thinking, and teamwork skills help you interpret data, provide medical guidance, and collaborate with cross-functional teams. These capabilities are vital to ensure patient safety, regulatory compliance, and the successful execution of clinical trials.

What are popular job titles related to Medical Advisor Medical Monitor jobs?

For Medical Advisor Medical Monitor jobs, the most frequently searched job titles are:

Infographic showing various Medical Advisor Medical Monitor job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 14% Part Time, and 6% Contract. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $112,014 per year, or $53.9 per hour.

Medical Scientific Advisor

Brooklyn, CT • On-site

Novotech
Guided Missile and Space Vehicle Manufacturing • 11 - 50 employees
Learn more about Novotechexternal

Full-time

Posted 26 days ago

Key responsibilities

  • Advise on protocol design, endpoints, inclusion/exclusion criteria, and study strategy.

  • Review protocols, CSRs, IBs, safety reports, and regulatory documents.

  • Support medical writing quality, participate in sponsor meetings, proposal reviews, and bid defenses.

Job description

The Medical Advisor is a senior scientific and medical expert responsible for providing strategic medical consultation across clinical development programs. The role advises on protocol design, study feasibility, endpoint selection, safety considerations, clinical development strategy, and medical writing deliverables including protocols, CSRs, IBs, regulatory submissions and publications. The position supports sponsor engagement, bid defenses, and cross-functional project teams. 

Responsibilities:

  • Advise on protocol design, endpoints, inclusion/exclusion criteria and study strategy. 

  • Review protocols, CSRs, IBs, safety reports and regulatory documents. 

  • Support medical writing quality and scientific accuracy. 

  • Participate in sponsor meetings, proposal reviews and bid defenses. 

  • Provide medical consultation for feasibility and business development opportunities. 

  • Support medical monitoring and safety-related discussions when required. 

  • Mentor teams and contribute to SOPs, training and scientific best practices.

Minimum Qualifications & Experience:

  • MD or PhD in Medicine, Life Sciences, Clinical Pharmacology or related field. 

  • Minimum 10 years relevant experience in CRO, biotech, pharma or academia. 

  • Strong expertise in protocol design, clinical development and medical writing. 

  • Experience with protocols, CSRs, IBs, regulatory documents and publications. 

  • Strong understanding of ICH-GCP and regulatory requirements. 

  • Excellent communication and client-facing skills.


Novotech is a global full-service clinical Contract Research Organization (CRO).


At Novotech, ambition meets opportunity. As a globally recognized leader in clinical research and scientific advisory services, we are proud to combine our position at the forefront of the industry with an award-winning workplace culture that values ambition, innovation, and growth. Named Employer of Choice, Great Place to Work and Employer of Choice for Gender Equality (EOCGE), we are committed to fostering an environment that reflects the life-changing work we do.

Since 1997, we have expanded our global footprint, now with 30+ offices across Asia-Pacific, the United States, and Europe. This growing network unites professionals from diverse backgrounds and disciplines to advance therapies that improve patient outcomes worldwide. 


At Novotech, our employees are at the heart of our success. By offering trust, flexibility, and autonomy through programs like NovoLife, our flexible benefits framework, we empower team members to create an effective work-life balance that delivers professional satisfaction and maximum results for clients.


With access to mentorship opportunities, professional development programs, and a dynamic community, Novotech offers a platform for driven individuals to achieve personal growth while shaping the future of healthcare. Join us to be a part of a team that values your contributions and supports your ambition to make a global impact.

At Novotech we have advanced therapeutic and regulatory expertise, the ability to execute across markets and a client-centric service model, so that our clients get a trusted, long-term partner and an accelerated path to bring their life-changing advances to market. This gives our employees the opportunity to develop their careers by joining a diverse and supportive global organization with a collaborative culture, whilst working with clients on the cutting-edge of life sciences. 
At Novotech you will work alongside empowered teams with a shared commitment to success.

  • Strategic vs transactional mindset.
  • Ability to gain insights and make proactive decisions quickly.
  • Culture that fosters partnership and collaboration, where every voice is heard and valued.
  • Ongoing support from senior stakeholders and leadership team.
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