Are you a detail-oriented and organized individual looking for a challenging role in clinical trial operations? 🌐 TRDFIN Support Services is seeking a Clinical Trial Specialist to support the planning, execution, and management of clinical trials in compliance with regulatory and ethical standards. Let’s dive into the details of this exciting opportunity! 💼
About the Job 🌈
As a Clinical Trial Specialist, you will play a critical role in supporting end-to-end clinical trial operations, from study start-up to close-out. You will work closely with internal teams, investigators, and external partners to ensure protocol adherence, maintain documentation, and ensure smooth collaboration. If you have a strong understanding of clinical trial processes and ICH-GCP guidelines, this could be the perfect opportunity for you. 📚
Key Responsibilities 📝
- Support end-to-end clinical trial operations: Coordinate trial activities, maintain documentation, and ensure compliance with regulatory requirements.
- Coordinate with investigators, CROs, and study sites: Ensure protocol adherence and smooth collaboration among internal teams, investigators, and external partners.
- Prepare, maintain, and manage essential trial documentation and study files: Ensure accurate and efficient management of trial documentation.
- Assist with site initiation, monitoring, and close-out activities: Support site initiation, monitoring, and close-out activities, ensuring compliance with ICH-GCP guidelines.
- Track study timelines, milestones, and deliverables: Ensure timely completion of study milestones and deliverables.
Required Skills & Qualifications 📚
- Bachelor’s degree in Life Sciences, Pharmacy, or a related field: Strong educational background in a relevant field.
- 2+ years of experience in clinical trial operations or clinical research: Practical experience in clinical trial operations or clinical research.
- Strong understanding of clinical trial processes and ICH-GCP guidelines: Excellent knowledge of clinical trial processes and ICH-GCP guidelines.
- Experience working with CROs, investigators, and clinical sites: Strong experience working with CROs, investigators, and clinical sites.
Tools & Systems (Preferred) 💻
- Clinical Trial Management Systems (CTMS): Experience with CTMS is preferred.
- Electronic Trial Master File (eTMF) systems: Experience with eTMF systems is preferred.
- Electronic Data Capture (EDC) systems: Experience with EDC systems is preferred.
- Microsoft Excel, Word, and PowerPoint: Strong proficiency in Microsoft Office.
Certifications (Nice to Have) 📜
- ICH-GCP Certification: Certification in ICH-GCP guidelines is a plus.
- Clinical Research Coordinator (CRC) certification: CRC certification is a plus.
- Clinical Trial Management certifications: Certifications in clinical trial management are a plus.
What We Offer 🌈
- Competitive compensation and benefits: TRDFIN Support Services offers competitive compensation and benefits.
- Exposure to global clinical trials and regulatory environments: Opportunity to work on global clinical trials and gain experience in regulatory environments.
- Opportunities for career growth: Opportunity for career growth in clinical research and operations.
- Collaborative and compliance-focused work culture: TRDFIN Support Services has a collaborative and compliance-focused work culture.
Apply Now 👇🏻:
https://www.linkedin.com/jobs/view/4343994131/
Conclusion 🌟
Don’t miss this opportunity to join TRDFIN Support Services and contribute to the success of clinical trials. Apply now and take the first step towards a rewarding career in clinical research! 🚀
