MS Clinical Research (MSCR) is a dynamic and forward-thinking clinical research organization dedicated to conducting cutting-edge clinical trials. We are committed to advancing medical science and contributing to the development of innovative healthcare solutions.
Job Summary
We are seeking enthusiastic and detail-oriented individuals to join our team as Clinical Research Coordinators. Candidates with a minimum 1-2 years of experience or a fresher.
Key Responsibilities
1. Study Coordination:
- Assist in the planning, initiation, and coordination of clinical trials under the supervision of the
Principal Investigator and study team.
- Ensure compliance with study protocols, Good Clinical Practice (GCP), and regulatory requirements.
2. Participant Recruitment and Screening:
- Identify and screen potential study participants.
- Coordinate participant recruitment activities and maintain accurate screening logs.
3. Informed Consent Process:
- Facilitate the informed consent process for study participants.
- Maintain documentation of informed consent and regulatory compliance.
4. Data Collection and Management:
- Collect and record study data accurately and in a timely manner.
- Ensure completeness and quality of data through routine checks and validations.
5. Site Management:
- Liaise with investigative sites and study teams to facilitate smooth study conduct.
- Assist in the preparation and submission of regulatory documents.
6. Safety Reporting:
- Monitor and report adverse events according to regulatory requirements.
- Collaborate with the study team to ensure the safety of participants.
7. Training and Development:
- Participate in training programs to develop a strong foundation in clinical research practices.
- Stay informed about relevant regulations and industry trends.
Requirements:
1. Education:
Bachelor's degree in a relevant life sciences field.
2. Skills and Qualities:
- Robust organizational and multitasking skills.
- Excellent communication and interpersonal skills.
- Detail-oriented with a commitment to accuracy.
3. Team Collaboration:
-Ability to work effectively in a collaborative team environment.
4. Commitment to Compliance:
-Understanding of ethical principles and a commitment to ensuring regulatory compliance.
5. Learning Agility:
-Demonstrated ability and willingness to learn and adapt in a fast-paced environment.
Benefits:
- Comprehensive training and mentorship program.
- Opportunities for professional growth and development.
- Competitive compensation and benefits package.
Join our team at MS Clinical Research and embark on a rewarding career in clinical research. This is an excellent opportunity to contribute to the advancement of medical science and make a meaningful impact on healthcare research.
📌 Clinical Research Coordinator (Bengaluru)
🏢 MS CLINICAL RESEARCH
📍 Bengaluru
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