Remote opportunity at
MMSSenior Medical Monitor (Remote - US)
MMS, an award-winning and data-focused clinical research organization that serves the biotechnology, pharmaceutical, and medical device sectors, seeks a remote Senior Medical Monitor. This position suits…
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About This Role
MMS, an award-winning and data-focused clinical research organization that serves the biotechnology, pharmaceutical, and medical device sectors, seeks a remote Senior Medical Monitor. This position suits medical professionals experienced in clinical trials who want to provide medical oversight and safety surveillance for global studies. MMS maintains a global presence across four continents and holds certification as a Great Place to Work organization. In this role, the professional will deliver medical…
Job Description
MMS, an award-winning and data-focused clinical research organization that serves the biotechnology, pharmaceutical, and medical device sectors, seeks a remote Senior Medical Monitor. This position suits medical professionals experienced in clinical trials who want to provide medical oversight and safety surveillance for global studies. MMS maintains a global presence across four continents and holds certification as a Great Place to Work organization.
In this role, the professional will deliver medical guidance across Phase I through Phase IV clinical trials and observational studies. Key duties involve evaluating participant eligibility, reviewing safety data, assisting with study documents, and participating in safety committees. The position requires functioning both independently and alongside client clinical and safety groups.
Responsibilities
- Deliver medical oversight across Phase I-IV clinical studies and observational projects
- Evaluate subject eligibility, protocol deviations, adverse events, lab findings, and vital signs
- Assist in developing protocols, Investigator Brochures, and Medical Monitoring Plans
- Address site inquiries and offer medical guidance during trial execution
- Engage in Data Monitoring Committees, Safety Review Committees, and cross-functional meetings
- Serve as the primary medical reviewer for individual adverse event reports
- Oversee safety surveillance, signal management, and cumulative safety information analysis
- Review safety sections of regulatory files and NDA or BLA submissions
- Act as a medical subject matter expert for sponsors and internal teams
Requirements
- Medical degree such as an MD, DO, or an international equivalent
- At least five years of medical monitoring, clinical, or research background
- Familiarity with protocol amendments and ICF updates
- Background in aggregate data review for active clinical trials
- Experience as a clinical scientist handling trial data assessment and safety surveillance for Phase I-III studies
- Familiarity with ICH, FDA, and EMA regulatory guidelines
- Proficiency in MS Office software
- Competency in medical terminology and clinical pharmacology
Core Skills
Frequently Asked Questions
Answers are based only on the employer’s listing; where it doesn’t say, neither do we.
Is this position remote?
Yes, the posting specifies that the role is remote within the United States.
What education is required for this job?
Applicants must hold a medical degree such as an MD, DO, or an international equivalent.
How much experience is needed?
The position requires five or more years of medical monitoring, clinical, or research experience.
What is the salary for this role?
The source posting does not specify a salary.
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