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MS CLINICAL
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Clinical Research Coordinator

Clinical Research Coordinator

MS CLINICAL

1 years

3 Lacs

India

Posted:5 days ago| Platform: GlassDoor logo

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Skills Required

research cutting development healthcare planning initiation coordination compliance gcp recruitment documentation data checks report training regulations multitasking communication collaborative learning compensation

Work Mode

On-site

Job Type

Part Time

Job Description

Job Title: Clinical Research Coordinator (minimum 1 year of experience)

Company: MS Clinical Research Pvt Ltd

About Us:

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 looking for enthusiastic and detail-oriented individuals to join our team as Clinical Research Coordinators. Only candidates with a minimum of 1-3 years of experience in BA/BE studies should apply.

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:

Education:

Bachelor's degree in a relevant life sciences field.

Skills and Qualities:

Strong organizational and multitasking skills.
Excellent communication and interpersonal skills.
Detail-oriented with a commitment to accuracy.

Team Collaboration:

Ability to work effectively in a collaborative team environment.

Commitment to Compliance:

Understanding of ethical principles and a commitment to ensuring regulatory compliance.

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.

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Clinical Research Coordinator