Health Care Global Enterprises (HCG) is a leading healthcare provider in India, specializing in oncology and cancer care. With a strong reputation for innovative treatment and research, HCG is committed to advancing medical science through high-quality clinical trials and research programs. The company is known for its state-of-the-art facilities, dedicated professionals, and patient-centric approach to healthcare.
Job Responsibilities
As a Clinical Research Coordinator at Health Care Global Enterprises, you will be responsible for ensuring the smooth execution of clinical trials. Key responsibilities include:
- Overseeing the trouble-free running of clinical trials.
- Collecting, coding, and analyzing research data.
- Managing budgets allocated for research projects.
- Communicating with participants regarding study objectives.
- Administering questionnaires and monitoring participants to ensure adherence to study protocols.
- Liaising with laboratories regarding research findings.
- Ensuring that the study complies with ethical and regulatory standards.
- Maintaining research records, including case report forms, drug dispensation records, and other regulatory documents per FDA guidelines.
- Directing the collection, labeling, storage, and transportation of all specimens.
- Ensuring that all necessary equipment and supplies for the study are available and in proper working order.
Qualifications Required
Candidates applying for the Clinical Research Coordinator position should meet the following qualifications:
- A Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Nursing, or a related field.
- 0-2 years of experience in clinical research or a related field.
- Familiarity with clinical trial regulations and ethical guidelines.
Key Skills
To succeed in this role, candidates should possess the following skills:
- Strong organizational and time management abilities.
- Excellent communication and interpersonal skills.
- Attention to detail and accuracy in data collection and analysis.
- Knowledge of clinical trial protocols and regulatory requirements.
- Proficiency in MS Office and clinical data management software.
