Clinical Site Manager
Há 2 dias
Clinical Site Manager – (Ophthalmology & Neurology Focus)
Location: Remote-based
We’re partnering with a global biopharmaceutical company dedicated to advancing treatments in Ophthalmology, Neurology , and other complex therapeutic areas. To support several ongoing and upcoming studies, we are seeking a Clinical Site Manager to oversee key investigator sites across LATAM .
This position is offering a unique opportunity to blend operational oversight with strong relationship management at the site level.
Key Responsibilities
- Serve as the primary sponsor contact for assigned sites and CRO monitors, ensuring high-quality communication and collaboration.
- Oversee site management activities across multiple studies, including start-up, monitoring, and close-out phases.
- Drive patient recruitment and retention initiatives, fostering engagement with Principal Investigators and site coordinators.
- Provide operational oversight of CRO CRAs to ensure adherence to protocol, timelines, and quality standards.
- Support the sponsor’s clinical operations alignment , ensuring consistency and excellence in study execution.
- Troubleshoot operational challenges and proactively address site-level issues to maintain study momentum.
- Ensure proper management of study supplies, documentation, and compliance with GCP and sponsor SOPs.
Requirements
- Proven experience as a Lead CRA , Senior CRA , or Clinical Site Manager with strong independent monitoring and site leadership skills.
- Therapeutic experience in Ophthalmology and/or Neurology is essential.
- Additional experience in Immunology, Rare Diseases, or Respiratory indications would be advantageous.
- Solid understanding of GCP , ICH Guidelines , and regional regulatory requirements across Eastern Europe.
- Excellent communication, relationship management, and problem-solving skills.
- Willingness to travel across assigned countries as required.
Why Join?
- Play a pivotal role in advancing innovative treatments that make a meaningful difference to patients’ lives.
- Work in a hands-on, strategic role bridging sponsor oversight and site engagement.
- Join an international, science-driven environment with opportunities for professional growth.
About Planet Pharma:
Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering.
Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.
We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.
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