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 aΒ Clinical Research CoordinatorΒ inΒ 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:
- Bachelorβs or Masterβs 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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