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Clinical Research Site Development Specialist
1 month ago
Job Summary
We are seeking an experienced professional to develop strategic relationships with clinical research sites, optimizing and advancing the progress of clinical trials.
Key Responsibilities:
- Maintain and refine internal site databases in collaboration with Study Startup, Clinical Operations, and Process Improvement.
- Participate in the development of improvement strategies for the site identification process, implementation, and related training activities.
- Define main study objectives and optimal site profiles.
- Create initial lists of potential sites.
- Communicate with project teams to fine-tune strategies and methodologies for initial and follow-up site contacts.
- Maintain study site identification trackers for further site evaluation and selection activities.
- Liaise with project teams to evaluate status and progress of site identification, identifying potential risks or issues.
- Perform due diligence checks of regulatory and legal limitations applicable to recommended investigators or clinical sites.
Requirements:
- University/college degree in Life Sciences, Pharmacy, RN, or Healthcare field (plus).
- Minimum 2 years of proven experience in Site Identification/Study Start-Up activities or equivalent.
- Understanding of Good Clinical Practice, local laws, and applicable regulations in Australia.
- Excellent communication and collaboration skills.
- Demonstrated ability to work in a dynamic environment under compressed deadlines.
About PSI:
We offer excellent working conditions, extensive training, and a supportive team. Join a company committed to prioritizing its employees and dedicated to investing in their ongoing professional growth and success.