
Junior Site Activation Coordinator
Posted 4 days ago

Posted 4 days ago
This is a fully remote position, open to applicants in Serbia, +1 more country.
• Execute site activation tasks for designated clinical studies in accordance with relevant regulations, standard operating procedures (SOPs), work instructions, and project requirements.
• Partner with Site Activation Managers, Project Management teams, and various functional groups to facilitate study start-up deliverables.
• Prepare, review, and uphold site regulatory documentation.
• Assess and manage essential study documents, escalating issues when necessary.
• Monitor regulatory submissions, ethics approvals, contractual documentation, Investigator Pack releases, and Informed Consent Form approvals.
• Distribute finalized regulatory and contractual documents to investigative sites and internal stakeholders.
• Maintain and refresh internal systems, databases, trackers, timelines, and project plans.
• Assist in the collection, filing, and upkeep of documents throughout the study start-up process.
• Help ensure compliance with Good Clinical Practice, regulatory standards, and company protocols.
• Foster and sustain productive relationships with internal teams, sponsors, and investigative sites.
• Bachelor's degree in Life Sciences, Healthcare, Pharmacy, Biotechnology, or a related discipline.
• Proficiency in English, both written and spoken.
• Excellent organizational and time-management abilities.
• Competence in Microsoft Office applications, including Word, Excel, PowerPoint, and Outlook.
• Exceptional attention to detail and the capability to manage multiple priorities at once.
• Strong interpersonal and communication skills.
• Prior experience in clinical research, clinical trials, site activation, regulatory affairs, or study start-up activities is preferred.
• Familiarity with Good Clinical Practice (GCP), ICH guidelines, and the drug development process is preferred.
• Experience with clinical trial management systems and document management platforms is preferred.
• Opportunity to develop a career in the clinical research sector.
• Comprehensive onboarding and training programs.
• Exposure to international clinical studies and cross-functional teams.
• Professional development and career advancement opportunities.
• A collaborative and inclusive work atmosphere.
• Modern office facilities located in Bratislava.
Hempel A/S
Hempel A/S
RTX
FLYACTS • Venture Studio für erfahrene Unternehmer
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