MS Clinical Research (MSCR) is a leading clinical research organization dedicated to pioneering advancements in medical science through innovative clinical trials. With a strong commitment to excellence, we aim to contribute to the development of groundbreaking healthcare solutions. At MSCR, we create opportunities for professionals to grow, learn, and impact the future of healthcare.
Job Responsibilities
As a Clinical Research Coordinator, you will play a vital role in ensuring the smooth execution of clinical trials. Your key responsibilities include:
1. Study Coordination
- Plan, initiate, and coordinate clinical trials under the guidance of the Principal Investigator.
- Ensure adherence to study protocols, Good Clinical Practice (GCP), and regulatory standards.
2. Participant Recruitment and Screening
- Identify and screen potential participants for the study.
- Organize recruitment activities and maintain detailed screening records.
3. Informed Consent Process
- Facilitate the informed consent process, ensuring ethical and regulatory compliance.
- Document and maintain accurate records of the consent process.
4. Data Collection and Management
- Accurately collect, record, and validate study data.
- Conduct regular checks to maintain data integrity and completeness.
5. Site Management
- Serve as a liaison between investigative sites and study teams.
- Assist with regulatory document preparation and submission.
6. Safety Reporting
- Monitor and report adverse events following regulatory requirements.
- Work with the study team to prioritize participant safety.
7. Training and Development
- Participate in training programs to enhance clinical research expertise.
- Stay updated on industry trends and regulatory changes.
Qualifications
To excel in this role, the following qualifications are required:
- A Bachelor’s degree in a relevant life sciences field.
- 1–3 years of experience in BA/BE studies.
Key Skills
Successful candidates should possess:
- Strong organizational and multitasking capabilities.
- Excellent communication and interpersonal skills.
- Attention to detail and a commitment to accuracy.
- A collaborative mindset to work effectively in a team.
- Understanding of ethical principles and regulatory compliance.
- Learning agility and adaptability in a fast-paced environment.
Benefits
Joining MS Clinical Research offers numerous advantages:
- Comprehensive training and mentorship programs.
- Ample opportunities for career growth and skill development.
- Competitive salary and benefits package.
