ProClin Research Private Limited is a leading organization dedicated to providing top-tier services in drug development. Our operational teams actively collaborate with clinical sites to ensure cost-effective and timely deliverables for our clients. By offering a variety of outsourcing models, we build flexible relationships with clients and serve as a one-stop solution for all research needs.
Job Responsibilities
As a Clinical Research Coordinator at ProClin Research Private Limited, you will be responsible for:
- Overseeing clinical trials and ensuring compliance with research protocols.
- Managing informed consent processes and ensuring ethical considerations are met.
- Conducting clinical research activities with accuracy and adherence to regulatory guidelines.
- Coordinating between investigators, sponsors, and site personnel for smooth trial execution.
- Maintaining and updating research documentation and data management systems.
- Monitoring patient safety and ensuring adherence to Good Clinical Practice (GCP) guidelines.
Qualifications
To be considered for the Clinical Research Coordinator role, candidates must meet the following qualifications:
- A Bachelor’s degree in Life Sciences, Healthcare, Nursing, or a related field.
- 1-2 years of experience in clinical research or clinical trials.
- Familiarity with regulatory requirements and clinical research guidelines.
- Strong knowledge of protocol management and informed consent procedures.
Required Skills
The ideal candidate should possess the following skills:
- Excellent organizational and time management abilities.
- Strong attention to detail and accuracy in data handling.
- Proficiency in clinical trial management and research methodologies.
- Effective communication skills for collaborating with cross-functional teams.
- Ability to work independently while maintaining high standards of compliance.
