Fast-track your career with exposure to global trials and diverse therapeutic areas.
Regular workshops on GCP, regulatory updates, and soft skills development.
Contribute directly to the development of life-saving therapies for patients.
Title: Clinical Research Coordinator (CRC)
Content:
Role Overview: Responsible for the day-to-day management of clinical trial activities at the site level.
Key Responsibilities:
Patient screening, recruitment, and enrollment.
Maintenance of Investigator Site Files (ISF) and source documentation.
Coordination with Ethics Committees and Sponsors.
Eligibility: B.Pharm, M.Pharm, or Life Sciences graduate with valid certification.
Title: Intern Clinical Research Coordinator
Content:
Role Overview: An entry-level position for fresh graduates looking to build a career in clinical research.
Key Responsibilities:
Assisting Senior CRCs in documentation and data entry.
Learning Good Clinical Practice (GCP) and regulatory guidelines.
Supporting patient follow-up and scheduling.
Eligibility: Freshers with Life Sciences background/Pharmacology.
Title: Project Manager
Content:
Role Overview: Oversees multiple clinical trials and sites to ensure they are delivered on time, within budget, and with high quality.
Key Responsibilities:
Strategic planning and site initiation.
Vendor management and sponsor communication.
Risk assessment and mitigation strategies.
Eligibility: 5+ years of experience in Clinical Research/Site Management.
Title: Quality Assurance (QA) Associate
Content:
Role Overview: Ensures that all clinical trials are conducted in compliance with SOPs, ICH-GCP, and regulatory requirements.
Key Responsibilities:
Conducting internal audits of investigator sites.
Reviewing data for accuracy and completeness.
Preparing sites for regulatory inspections (FDA/CDSCO).
Eligibility: Experience in Clinical Quality Assurance or Compliance.
If you are passionate about clinical research and meet the eligibility criteria, we want to hear from you. Please fill out the form and upload your CV.
