Are you a passionate individual with a background in life sciences or pharmacy? OrciVita Sciences & Research Pvt. Ltd. is hiring for the position of Clinical Research Coordinator (CRC) in Kolkata and Bhubaneswar. This is a full-time opportunity for freshers and experienced professionals alike to contribute to groundbreaking clinical research. If you are detail-oriented, possess strong communication skills, and have a keen interest in clinical trials, this role is perfect for you. Read on to learn more about the job responsibilities, qualifications, and how to apply.
About OrciVita Sciences & Research Pvt. Ltd.
OrciVita Sciences & Research Pvt. Ltd. is a leading name in the field of clinical research, dedicated to advancing healthcare through innovative studies and trials. With a strong commitment to ethical practices and regulatory compliance, OrciVita is at the forefront of delivering high-quality research outcomes.
Job Title: Clinical Research Coordinator (CRC)
Location: Kolkata, Bhubaneswar
Job Type: Full-Time
Key Responsibilities
As a Clinical Research Coordinator (CRC), you will play a pivotal role in the successful execution of clinical trials. Your responsibilities will include:
- Patient Screening & Recruitment: Identifying and enrolling eligible participants for clinical trials.
- Informed Consent Process: Ensuring participants fully understand the study and voluntarily provide consent.
- Study Coordination: Managing day-to-day activities of clinical trials, ensuring adherence to protocols.
- Regulatory Compliance: Maintaining compliance with ICH-GCP, CDSCO, and other regulatory guidelines.
- Data Collection & Reporting: Accurately collecting, recording, and reporting clinical trial data.
- Safety Monitoring: Monitoring participant safety and reporting adverse events.
- Investigational Product & Sample Handling: Managing investigational products and biological samples as per protocols.
- Communication & Collaboration: Liaising with investigators, sponsors, and other stakeholders.
- Training & Development: Staying updated with industry trends and participating in training programs.
Required Qualifications & Skills
To excel in this role, you should possess the following:
- Education: Bachelor’s or Master’s degree in Life Sciences, Pharmacy, or a related field.
- Experience: Freshers with relevant qualifications are encouraged to apply.
- Regulatory Knowledge: Familiarity with ICH-GCP, CDSCO, and clinical trial regulations in India.
- Technical Skills: Proficiency in data entry and MS Office tools.
- Soft Skills: Strong communication, attention to detail, and the ability to multitask effectively.
How to Apply
If you meet the qualifications and are excited about this opportunity, send your updated resume to hrorcivita@gmail.com. Don’t miss the chance to be part of a dynamic team driving innovation in clinical research.