Are you an organized, detail-oriented professional with experience in clinical trials? MEDICEPTION is seeking a Clinical Trial Coordinator to manage and support clinical trial operations. This full-time, on-site role offers an exciting opportunity for professionals passionate about research, healthcare, and project management.
Company Introduction: Why Choose MEDICEPTION?
MEDICEPTION is a forward-thinking company in the healthcare and pharmaceutical industry, dedicated to advancing clinical research through efficient, well-managed trials. By joining MEDICEPTION, you’ll become part of a team committed to integrity, innovation, and scientific excellence, contributing to impactful research that supports healthcare improvements.
Responsibilities in the Clinical Trial Coordinator Role
The Clinical Trial Coordinator plays a crucial role in the success of clinical trials. This position involves a variety of tasks designed to keep trials on track, ensure compliance, and manage trial operations effectively. Key responsibilities include:
- Overseeing Clinical Trials: Ensure trials run smoothly, overseeing daily operations and troubleshooting issues.
- Communication and Coordination: Maintain clear communication with stakeholders, including trial sites, sponsors, and regulatory bodies.
- Protocol Development: Contribute to the development of clinical protocols, ensuring alignment with industry standards.
- Research and Data Collection: Conduct research and data collection as needed, contributing to the trial’s success.
- Trial Monitoring and Site Visits: Perform site visits and monitor trial progress to ensure adherence to protocols.
- Project Management: Manage timelines, budgets, and resources, keeping trials on schedule and within budget.
Qualifications: What You Need to Succeed
To thrive as a Clinical Trial Coordinator at MEDICEPTION, candidates must possess a solid educational background and relevant experience in clinical trials. Required qualifications include:
- Education: A Master’s degree in a relevant field (such as life sciences, clinical research, or healthcare).
- Experience: 3-4 years in clinical trial research, particularly in the pharmaceutical or healthcare industry.
- Knowledge: Familiarity with clinical trial processes, protocol development, and project management principles.
Skills: Essential Attributes for the Role
Success in this role also requires strong technical and interpersonal skills:
- Communication Skills: Ability to communicate effectively with team members, stakeholders, and trial participants.
- Organizational Skills: Strong organizational abilities to manage multiple tasks and keep trials running smoothly.
- Attention to Detail: Meticulous attention to detail to maintain data accuracy and adherence to protocols.
- Problem-Solving Abilities: Proactive approach to identifying and resolving issues as they arise.
Send in your CV at bhawana@mediception.com
