MSCR Hiring for Clinical Research Coordinator

MSCR Hiring for Clinical Research Coordinator

Are you passionate about advancing medical science through innovative clinical trials? MS Clinical Research Pvt Ltd, based in Bengaluru, Karnataka, is hiring for the role of Clinical Research Coordinator. This role is ideal for experienced professionals seeking to make a meaningful impact in healthcare research. MSCR Hiring for Clinical Research Coordinator

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Position Overview

• Position: Clinical Research Coordinator
• Location: Bengaluru, Karnataka, India
• Experience: 3–5 years (preferably in BA/BE studies)
• Qualification: B.Pharm, M.Pharm, Pharm.D, MSc, BSc, or a related Life Sciences field

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Key Responsibilities

Study Coordination

• Plan, initiate, and coordinate clinical trials in collaboration with the Principal Investigator and study team.
• Ensure adherence to Good Clinical Practice (GCP) and study protocols.

Participant Recruitment and Screening

• Identify and screen potential study participants.
• Manage recruitment activities and maintain accurate participant logs.

Informed Consent Process

• Facilitate the informed consent process and maintain comprehensive records of compliance.

Data Collection and Management

• Collect and record accurate study data while ensuring completeness and quality.
• Conduct routine data validation and checks.

Site Management

• Coordinate with investigative sites to ensure smooth study execution.
• Prepare and submit regulatory documentation as required.

Safety Reporting

• Monitor and report adverse events in accordance with regulatory guidelines.
• Collaborate with the study team to ensure the safety of participants.

Training and Development

• Participate in ongoing training to enhance expertise in clinical research practices.
• Stay informed about regulatory changes and industry trends.

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Qualifications and Skills

Educational Requirements

• Bachelor’s or Master’s degree in Life Sciences, Pharmacy, or related fields.

Experience

• Minimum of 3-5 years in clinical research with a focus on BA/BE studies.

Core Skills

• Strong knowledge of study coordination and regulatory compliance.
• Proficiency in data collection and validation.
• Excellent communication and interpersonal abilities.
• Detail-oriented with a commitment to accuracy and compliance.
• Ability to work collaboratively in a team environment.

Key Attributes

• Learning agility and adaptability in a fast-paced environment.
• Strong understanding of ethical principles and participant safety.

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Why Join MS Clinical Research?

• Be part of a pioneering organization that drives innovation in healthcare research.
• Collaborate with a dynamic team dedicated to maintaining the highest standards of quality and compliance.
• Contribute to groundbreaking clinical trials that advance medical science and improve patient outcomes.

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How to Apply

• Submit your application through the verified online portal. Ensure your resume highlights your experience in clinical trial coordination, data management, and regulatory compliance.

This is an excellent opportunity for professionals eager to advance their careers in clinical research and make a tangible impact on healthcare innovation. Join MS Clinical Research Pvt Ltd and be part of a transformative journey in medical science! MSCR Hiring for Clinical Research Coordinator

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