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Clinical Research Professional
3 weeks ago
As a Clinical Research Associate, you will be responsible for managing clinical studies from initiation to close-out. Your role will involve working closely with site staff to ensure compliance with Good Clinical Practice and study protocols.
- Key Responsibilities:
- Study Management:
- Manage the selection, initiation, and monitoring of study sites to ensure timely completion of assigned clinical studies.
- Collaborate with site staff to ensure they understand study protocols and requirements.
- Conduct pre-study visits to assess site eligibility and prepare study initiation visit reports.
- Ensure Principal Investigator/study staff complies with safety reporting requirements and tracks study recruitment to meet target goals.
- Conduct monitoring visits according to Standard Data Verification (SDV) plans and address any issues that arise.
- Training and Development:
- Provide ongoing training to site staff on ICH-GCP, GCP, study protocols, and requirements.
- Lead site initiation visits to ensure thorough understanding of study protocols and requirements among site staff.
- Documentation and Compliance:
- Ensure timely collection of essential documents in compliance with protocol and regulations at study start-up, during, and at study close-down.
- Prepare and complete study records' archiving according to sponsor requirements.
- Qualifications:
- Bachelor degree or above in Medical, Pharmacology, or Biology-related major.
- Minimum 1 year of experience as a Clinical Research Associate.
- Excellent knowledge of Good Clinical Practice and clinical trial operation processes/procedures.
- Strong skills in Microsoft Office applications (Word, Excel, PowerPoint, Outlook).
This is an exciting opportunity for a motivated and detail-oriented professional to join our team as a Clinical Research Associate
Why this role?
This role offers a unique blend of project management, scientific expertise, and people skills, making it an excellent fit for individuals who enjoy working collaboratively and taking ownership of complex projects.
About the ideal candidate:
We are looking for a highly organized and communicative individual with strong analytical skills and attention to detail. The ideal candidate will have a passion for learning and staying up-to-date with industry developments.
The benefits:
• Competitive salary and benefits package
• Opportunities for career growth and professional development
• Collaborative and dynamic work environment
How to apply:
To learn more about this exciting opportunity, please submit your application along with your resume and a cover letter explaining why you would be the perfect fit for this role.
