Kharghar Navi Mumbai Maharashtra Clinical research coordinator Jobs – 4 Open Jobs Today

Clinical Research Co-ordinator
SUNACT CANCER INSTITUTE PRIVATE LIMITED —Thane, Maharashtra
- ₹25,570.09 - ₹31,374.66 a month
- Full-time
- Microsoft Office
- Master's degree
- Databases
Quick apply
Randomization & Study Product Coordinator
Medpace, Inc. —Navi Mumbai, Maharashtra
- Full-time
- Microsoft Excel
- Bachelor's degree
- Paid time off
National Director, Sites - India
Iterative Health —Mumbai, Maharashtra
- PMP
- B.Sc
- Master's degree
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This enables us to offer a comprehensive range of services including drug discovery solutions, process & pharmaceutical development services, clinical trial…

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Clinical Research Co-ordinator

SUNACT CANCER INSTITUTE PRIVATE LIMITED
Thane, Maharashtra

Quick apply

Job details

Full-time
₹25,570.09 - ₹31,374.66 a month

Qualifications

Clinical research
Biotechnology
Microsoft Office
Master's degree
Databases
Bachelor's degree
Data entry
Organisational skills
Clinical trials
Communication skills
Nursing

Full job description

Key ResponsibilitiesStudy Coordination

Coordinate clinical trials and research projects from initiation to close-out.
Assist Principal Investigators (PIs) in study planning and execution.
Ensure adherence to approved study protocols and timelines.
Schedule and coordinate study visits, assessments, and follow-ups.

Participant Management

Screen, recruit, and enroll eligible study participants.
Conduct informed consent processes as per protocol and ethical guidelines.
Maintain regular communication with participants throughout the study.
Track participant compliance and retention.

Regulatory & Compliance

Maintain essential study documents and regulatory files.
Ensure compliance with ICH-GCP, CDSCO, NABH, and institutional requirements.
Prepare and submit documentation to Ethics Committees/IRBs.
Report protocol deviations, adverse events, and serious adverse events as required.

Data Management

Collect, verify, and maintain accurate study data.
Complete Case Report Forms (CRFs) and electronic data capture systems.
Ensure timely data entry and query resolution.
Maintain confidentiality and data integrity.

Sponsor & Site Coordination

Coordinate with sponsors, CROs, monitors, and study teams.
Support site initiation, monitoring, and audit visits.
Facilitate study-related training and meetings.

Documentation & Reporting

Maintain Trial Master Files (TMF) and Investigator Site Files (ISF).
Prepare study progress reports and recruitment updates.
Ensure all study records are audit-ready.

QualificationsEducation

Bachelor's or Master's degree in Life Sciences, Pharmacy, Biotechnology, Clinical Research, Nursing, or related healthcare field.

Experience

1–5 years of experience as a Clinical Research Coordinator or Clinical Research Associate.
Experience in oncology clinical trials will be preferred.
Experience handling regulatory documentation and ethics committee submissions.

Required Skills

Knowledge of ICH-GCP guidelines and clinical trial regulations.
Strong documentation and organizational skills.
Proficiency in Microsoft Office and clinical trial databases.
Excellent communication and stakeholder management skills.
Ability to manage multiple studies simultaneously.
Attention to detail and compliance-focused approach.

Key Performance Indicators (KPIs)

Study enrollment and retention rates.
Protocol compliance and audit readiness.
Timely regulatory submissions.
Data quality and query resolution timelines.
Sponsor and investigator satisfaction.

Pay: ₹25,570.09 - ₹31,374.66 per month

Work Location: In person

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clinical research coordinator jobs in kharghar navi mumbai maharashtra

Clinical Research Co-ordinator

Randomization & Study Product Coordinator

National Director, Sites - India

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