ProClin Research Private Limited is a leading clinical research organization dedicated to delivering high-quality services throughout the drug development lifecycle. The company ensures strict adherence to protocols, timelines, and budgets while maintaining operational excellence. With a hands-on approach and on-site operational teams, ProClin Research provides cost-effective solutions through flexible outsourcing models.
Job Description
ProClin Research is seeking a Clinical Research Coordinator in Raipur, Chhattisgarh, India to oversee clinical trial activities, ensuring compliance with study protocols and regulatory requirements.
Key Responsibilities:
- Obtain and manage informed consent from study participants.
- Ensure protocol adherence and regulatory compliance.
- Coordinate clinical trial activities, including patient recruitment and follow-ups.
- Maintain accurate documentation and case report forms (CRFs).
- Liaise with investigators, sponsors, and ethics committees.
- Monitor study progress and report adverse events (AEs/SAEs).
- Ensure data integrity and confidentiality.
Qualifications & Skills:
- Bachelor’s or Master’s degree in Life Sciences, Nursing, Pharmacy, or Public Health.
- Experience in Informed Consent and Protocol adherence
- Strong understanding of GCP (Good Clinical Practice) guidelines.
- Excellent organizational and time management skills.
- Attention to detail and ability to work independently.
Why Join ProClin Research?
- Work in a dynamic clinical research environment.
- Gain hands-on experience in drug development and clinical trials.
- Opportunity to collaborate with leading researchers and pharmaceutical companies.
How to Apply?
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