Trainee - Clinical Research Coordinator

**Job Description: Clinical Research Trainee**

**Position Overview**: A Clinical Research Trainee is an entry-level role within the field of clinical research, responsible for assisting in the planning, coordination, and execution of clinical trials and research studies aimed at evaluating the safety, efficacy, and effectiveness of new medical treatments, devices, and interventions. The role involves working closely with experienced clinical researchers, investigators, and various healthcare professionals to gain hands-on experience in all aspects of the clinical research process.

**Key Responsibilities**:
**Study Preparation**:

- Assist in the development of study protocols, informed consent forms, and other essential study documents.
- Contribute to the preparation of study materials, including case report forms (CRFs) and study binders.
- Assist in obtaining regulatory approvals and ethical review board (IRB/ethics committee) submissions.

**Participant Recruitment and Enrollment**:

- Help identify potential study participants by screening medical records and databases.
- Assist in recruiting eligible participants and obtaining their informed consent.
- Schedule participant visits and coordinate necessary assessments and tests.

**Data Collection and Monitoring**:

- Collaborate in the collection and recording of accurate and reliable data during participant visits.
- Perform data entry, ensuring completeness and accuracy of collected information.
- Assist in monitoring participant safety and well-being throughout the study.

**Clinical Trial Execution**:

- Support study coordinators in managing study visits, following study protocols and guidelines.
- Assist in maintaining study-related documentation, such as source documents and study logs.
- Participate in data verification, source document verification (SDV), and quality control activities.

**Communication and Collaboration**:

- Maintain effective communication with study team members, investigators, and study participants.
- Attend study team meetings, providing updates on study progress and challenges.

**Regulatory Compliance**:

- Ensure adherence to regulatory requirements and guidelines throughout the study.
- Assist in maintaining accurate and up-to-date regulatory documents.

**Professional Development**:

- Participate in training sessions and workshops to enhance knowledge of clinical research principles, regulations, and practices.
- Stay informed about industry trends and advancements in clinical research.

**Administrative Tasks**:

- Assist in organizing and archiving study-related documentation.
- Help with logistics such as ordering and maintaining supplies needed for the study.

**Qualifications and Requirements**:

- Bachelor's degree in a relevant scientific field (e.g., life sciences, nursing, pharmacy, etc.).
- Strong interest in clinical research and a desire to learn and develop within the field.
- Good organisational skills and attention to detail.
- Excellent interpersonal and communication skills.
- Basic understanding of medical terminology and research methodologies.
- Familiarity with Microsoft Office suite and data entry software.
- Ability to work effectively both independently and as part of a team.
- Ethical and responsible conduct in handling sensitive and confidential information.
- Flexibility to adapt to changing priorities and responsibilities.

**Job Type**: Internship
Contract length: 12 months

**Salary**: From ₹20,000.00 per month

**Speak with the employer**
+91 9021896890