Neurology Medical Monitor (Project-Based) – Remote

MMS Holdings Inc; United Kingdom; Remote; GBP 70,000 - 90,000; Part time

Job summary

A leading clinical research organization is seeking a medical monitoring professional for a project-based consulting role. The ideal candidate has a medical degree, specialized experience in Neurology, and over 5 years in clinical or research settings. Responsibilities include conducting medical monitoring tasks and leading safety activities. This role offers a chance to make significant contributions to clinical research efforts.

Qualifications

• 5+ years of clinical/research experience required.
• Specialty in Neurology or comparable experience.
• Relevant experience in medical monitoring within the pharmaceutical industry.

Responsibilities

• Conduct eligibility reviews and safety data reviews.
• Develop Medical Monitor Plan and participate in safety review meetings.
• Lead safety activities and provide medical input on study documents.

Skills

Medical monitoring

Scientific writing

Communication skills

Clinical data understanding

MS Office proficiency

Knowledge of regulatory practices

Education

Medical degree (MD or equivalent)

Job description

Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team?MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research.
Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit www.mmsholdings.comor follow MMS on LinkedIn.

This role is a project-based consulting opportunity to conduct medical monitoring on an as-needed basis. This is not a full-time position.

Roles & Responsibilities

• Responsible for medical monitoring tasks, which may include:
  • Eligibility review
  • Review of safety-related protocol‑related deviations
  • Review of safety data
  • Develop Medical Monitor Plan
  • Participation in medical monitoring and/or safety review meetings as needed
  • Medical management of queries
  • Medical coding review
  • Maintain records and logs
  • Medical review of study documents
• Provide medical input throughout the development process
• Provide medical input into the development and execution of study documents and plans, such as study protocol, IB, SMP, DMP, SAP, Lab manuals, etc.
• Provide significant expertise as primary medical reviewer of individual adverse event reports, clinical, and safety documents
• Lead safety activities on assigned product(s) that may include interactions with other functional groups inthecompany
• Responsible for strategies in pre and post marketing risk management, as well as keeping abreast of pharmacovigilance methods and trends in published literature and global regulations
• Responsible for strategies in monitoring and analysis of cumulative safety information
• Maintains significant knowledge of global and local regulations and guidance as they pertain to medical review and safety reporting

Job Requirements

• Medical degree required (MD or equivalent)
• Specialty in Neurology or comparable experience in Neurology
• 5 or more yearsof clinical experience and/ or research experience required
• Relevant experience in medical monitoring and/or medical reviewer in pharmaceutical industry
• Excellent scientific writing skills
• Ability to understand clinical data
• Proficiency with MS Office applications
• Good communication skills
• Strong knowledge of current regulatory practices and domestic and international regulations