Position: Clinical Research Coordinator

Location: Mumbai, India

Are you passionate about making a difference in healthcare? Do you possess a keen eye for detail and a drive for excellence? We are seeking dedicated individuals to join our team as Clinical Research Coordinators in Mumbai. This role offers a unique opportunity to contribute to cutting-edge medical research while advancing your career in a dynamic and collaborative environment.

Job Summary: As a Clinical Research Coordinator, you will play a pivotal role in the execution of clinical trials and research studies. Working closely with investigators, sponsors, and other stakeholders, you will ensure the smooth conduct of research activities while adhering to regulatory requirements and ethical standards. This multifaceted role requires strong organizational skills, attention to detail, and a commitment to maintaining the highest standards of quality and integrity.

Key Responsibilities:

1. Study Coordination: Coordinate all aspects of clinical trials from initiation to completion, including participant recruitment, scheduling visits, and obtaining informed consent.
2. Regulatory Compliance: Ensure compliance with regulatory requirements, including Good Clinical Practice (GCP) guidelines, and maintain study documentation in accordance with standard operating procedures (SOPs).
3. Data Management: Collect, record, and manage study data accurately and confidentially, utilizing electronic data capture systems and maintaining data integrity throughout the study duration.
4. Participant Interaction: Serve as the primary point of contact for study participants, providing support, answering inquiries, and ensuring their safety and well-being throughout the research process.
5. Protocol Adherence: Implement study protocols and procedures effectively, including the administration of study interventions and the collection of biological specimens, in strict accordance with protocol requirements.
6. Collaboration: Collaborate closely with investigators, study teams, and external partners to ensure seamless communication and coordination of study activities.
7. Quality Assurance: Perform quality checks and audits to monitor study conduct and compliance, identifying and addressing any deviations or discrepancies in a timely manner.
8. Safety Monitoring: Monitor participant safety and adverse events, reporting any concerns or incidents promptly and following established reporting procedures.
9. Training and Development: Stay informed about relevant regulations, guidelines, and industry trends through ongoing training and professional development activities.

Qualifications:

• Bachelor's degree in life sciences, pharmacy, nursing, or a related field. (For fresher candidates)
• Prior experience in clinical research coordination or related field preferred. (For experienced candidates)
• Strong communication and interpersonal skills, with the ability to interact effectively with diverse stakeholders.
• Excellent organizational skills and attention to detail, with the ability to manage multiple tasks simultaneously.
• Proficiency in Microsoft Office applications and electronic data capture systems.
• Understanding of ethical principles and regulatory requirements governing clinical research.
• Ability to work independently and as part of a team in a fast-paced environment.

Age and Gender Inclusivity: We welcome applications from individuals of all ages (18 years to 60 years) and genders, including male, female, and non-binary individuals. Diversity and inclusivity are core values of our organization, and we are committed to providing equal opportunities for all qualified candidates.

If you are ready to take the next step in your career and contribute to groundbreaking research that has the potential to improve patient outcomes and advance medical science, we encourage you to apply now. Click on the "Apply For Job" button to submit your application and join us on our mission to make a positive impact in healthcare.