Clinical Research Coordinator at Hector Research and Archival Private Limited
If you’re passionate about clinical research and looking for an exciting role where you can contribute to meaningful studies, Hector Research and Archival Private Limited (HRAPL) is seeking a Clinical Research Coordinator to join their team in Rishikesh, Uttarakhand. This position offers the opportunity to work in an evolving environment that focuses on ensuring high-quality clinical trials and patient care. Clinical Research Coordinator at Hector Research and Archival Private Limited
Here’s everything you need to know about this opportunity:
Key Details at a Glance
Position | Clinical Research Coordinator |
---|---|
Company | Hector Research and Archival Private Limited |
Location | Rishikesh, Uttarakhand |
Experience | 2 to 3 Years |
Qualification | B.Pharm, M.Pharm, Pharm.D, MSc, BSc, Lifesciences |
Salary | Competitive |
Apply | Send CVs to hr@hrapl.in |
Job Posted on | October 5, 2024 |
Why Join HRAPL?
HRAPL is a leading Site Management Organization (SMO), known for its commitment to conducting efficient and compliant clinical research. By joining as a Clinical Research Coordinator, you’ll be part of a team dedicated to innovation and patient-centered research. This role offers flexibility, problem-solving opportunities, and a work-life balance, allowing you to grow both professionally and personally. Clinical Research Coordinator at Hector Research and Archival Private Limited
What You’ll Do as a Clinical Research Coordinator
In this role, you’ll play a vital part in the execution of clinical trials, ensuring they run smoothly and ethically. Your responsibilities will include:
1. Study Coordination Clinical Research Coordinator at Hector Research and Archival Private Limited
You’ll be responsible for overseeing clinical trials, from planning to execution. This involves managing patient recruitment, enrollment, and retention to ensure that studies meet their objectives within the specified timelines.
2. Patient Recruitment & Management Clinical Research Coordinator at Hector Research and Archival Private Limited
Working closely with patients and clinical teams, you’ll manage the recruitment process, ensure smooth enrollment, and ensure that patients are engaged and retained throughout the clinical trial.
3. Data Collection & Management Clinical Research Coordinator at Hector Research and Archival Private Limited
Accurate data is critical in clinical research. You will collect, enter, and manage data from clinical studies, ensuring it meets the necessary standards for quality and compliance. You’ll also be responsible for ensuring the integrity of the data collected.
4. Communication & Collaboration Clinical Research Coordinator at Hector Research and Archival Private Limited
You’ll serve as a key link between clinical teams, sponsors, and regulatory authorities. You’ll regularly communicate the status of the trials, handle queries, and ensure that everyone is on the same page for a successful study outcome.
5. Compliance with GCP & Regulations Clinical Research Coordinator at Hector Research and Archival Private Limited
Ensuring that the trials comply with Good Clinical Practice (GCP) and relevant regulatory requirements will be essential. You’ll work to maintain high ethical standards in line with global clinical research protocols.
Qualifications and Experience Required
To succeed in this role, candidates should meet the following eligibility criteria:
- Education: Bachelor’s or Master’s degree in Life Sciences, Medical Sciences, or a related field from an accredited institution. This includes degrees such as B.Pharm, M.Pharm, Pharm.D, MSc, and BSc in relevant fields.
- Experience: You must have a minimum of 2-3 years of experience in clinical research. Prior experience in study coordination, patient recruitment, and data management is essential.
What Makes This Role Stand Out?
- Competitive Salary: HRAPL offers a competitive salary package that reflects your experience and qualifications, ensuring you are well-rewarded for your contributions.
- Work-Life Balance: HRAPL emphasizes the importance of time management and flexibility, allowing you to balance your work with personal commitments.
- Growth Opportunities: This role is perfect for someone looking to advance in the clinical research field. With hands-on experience and exposure to various aspects of clinical trials, you’ll gain invaluable skills and expertise.
How to Apply
If this role excites you and you’re ready to take on a fulfilling challenge, send your CV to hr@hrapl.in. Make sure to highlight your experience in clinical research and your key achievements in study coordination, patient management, and regulatory compliance.
This is an opportunity to not only develop your career but also to be a part of meaningful research that impacts lives. If you’re ready to make a difference, apply today!
Final Thoughts
Becoming a Clinical Research Coordinator at HRAPL means stepping into a role where every task you perform is crucial to the success of clinical trials. From recruiting patients to ensuring regulatory compliance, you’ll be an integral part of advancing medical research. If you have the required experience and qualifications, this is your chance to join a reputable organization that values innovation, quality, and teamwork.