Medical monitor clinical trials medical affairs Job at Sanaclis US, LLC, Florida

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  • Sanaclis US, LLC
  • Florida

Job Description

We Are Hiring!

We are looking for a Part-Time, Medical Monitor Freelancer (1099 position) to strengthen our Medical Affairs Department at SanaClis.

Job Requirements:

  • Medical degree or equivalent combination of education and expertise
  • 2+ years of experience in Medical Affairs (or at least 3 years of combined experience in Medical Affairs, drug safety, or clinical development) within the pharmaceutical industry, with the ability to work autonomously
  • Previous experience in ophthalmology
  • Knowledge of Spanish (in addition to English)
  • Profound knowledge of ICH GCP, GVP guidelines, and relevant regulatory requirements
  • Ability to review and interpret medical information and safety data (including MedDRA and WHO Drug coding)
  • Strong analytical and critical thinking skills, with excellent interpersonal communication
  • English language proficiency of minimum level B2 (ref. CEFR) – fluent in written and spoken English
  • Ability to independently find and apply territory-specific guidelines and standard practices in medical affairs and pharmacovigilance.
  • Advanced proficiency in Microsoft Office Suite (Word, Excel, PowerPoint), email, and telecommunication tools
  • Willingness and ability to travel, as needed

Job Responsibilities:

  • Serving as the medical expert and providing support to project teams for assigned clinical trials
  • Reviewing patient data from clinical trials to ensure consistency with protocols and high data quality
  • Monitoring adverse events, conducting necessary follow-up, and ensuring timely communication of critical medical information to sites
  • Assisting in the development of safety reports, clinical trial documents, and training materials, as needed
  • Ensuring compliance with ICH GCP, GVP, local regulations, and SanaClis/Customer SOPs
  • Staying current with guidelines and standard practices in medical affairs and pharmacovigilance for the relevant territory
  • Providing medical guidance during audits or inspections
  • Maintaining high professional and ethical standards in all interactions with authorities, Clients, and colleag

What We Offer:

  • Competitive Pay – Fair compensation based on your skills and experience
  • Friendly Environment – Work in a privately owned international company
  • Mentorship and Guidance – Collaborate with senior team members and enhance your learning

Please Note: This is a contract (1099) position.

You can apply via the link or send your CV directly to: careers@sanaclis.com

* SanaClis is an equal employment opportunity employer. We value diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity or expression, religion, national origin, ancestry, age, disability, marital status, pregnancy, protected veteran status, order of protection status, protected genetic information, or any other characteristic protected by law.

Job Types: Full-time, Part-time

Expected hours: 10 – 30 per week

Schedule:

  • Monday to Friday

Experience:

  • Medical Affairs: 2 years (Required)
  • MedDRA and WHO Drug Coding: 2 years (Preferred)
  • Ophthalmology: 1 year (Required)

Work Location: Remote

Job Tags

Remote job, Full time, Contract work, Part time, Freelance, Local area, Monday to Friday,

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