MSCR Hiring Clinical Research Coordinator

MS Clinical Research (MSCR) Pvt Ltd is a pioneering clinical research organization committed to conducting innovative and impactful clinical trials. Our mission is to advance medical science and support the development of groundbreaking healthcare solutions. As a dynamic and forward-thinking organization, we strive to uphold the highest standards of quality and compliance in clinical research.

Responsibilities

As a Clinical Research Coordinator, you will play a vital role in the success of clinical trials by ensuring smooth study execution and compliance with regulatory standards. Below are the main responsibilities:

1. Study Coordination:
   • Assist in planning, initiating, and coordinating clinical trials under the guidance of the Principal Investigator and study team.
   • Ensure adherence to study protocols, Good Clinical Practice (GCP), and regulatory requirements.
2. Participant Recruitment and Screening:
   • Identify and screen potential study participants.
   • Manage recruitment activities and maintain accurate participant screening logs.
3. Informed Consent Process:
   • Facilitate the informed consent process for study participants.
   • Document and maintain records of informed consent and regulatory compliance.
4. Data Collection and Management:
   • Accurately collect and record study data.
   • Conduct routine data checks to ensure completeness and quality.
5. Site Management:
   • Coordinate with investigative sites and study teams to ensure seamless study conduct.
   • Assist in the preparation and submission of regulatory documentation.
6. Safety Reporting:
   • Monitor and report adverse events in compliance with regulatory guidelines.
   • Collaborate with the study team to ensure participant safety.
7. Training and Development:
   • Participate in training programs to build expertise in clinical research practices.
   • Stay updated on relevant regulations and industry trends.

Qualifications

• Bachelor’s degree in a relevant life sciences field.
• Minimum of 3-5 years of experience in BA/BE studies.
• Strong organizational and multitasking abilities.
• Excellent communication and interpersonal skills.
• Detail-oriented with a commitment to accuracy and compliance.
• Ability to work effectively in a collaborative team environment.

Key Skills

• Proficiency in study coordination and regulatory compliance.
• Competence in data collection and validation.
• Strong understanding of ethical principles and commitment to participant safety.
• Learning agility and adaptability in a fast-paced environment.

Application Link