Medi Pharma Group

Vacancy Details

Urgently Required: Clinical Research Coordinators (CRCs)

Hospital: Medi Pharma Group

Location: Gandhinagar

Experience: 1 to 5 years

Number of Vacancies: 1

Free registration • Verified hospital jobs • One profile for many jobs

Clinical Research Coordinators (CRCs) play a vital role in the conduct of clinical trials, acting as the linchpin between the trial’s operations and its success.
They manage the day-to-day responsibilities of clinical studies, ensuring compliance with protocols, ethical guidelines, and regulatory requirements.
CRCs coordinate activities to recruit participants, collect data, and maintain accurate records, working closely with investigators, participants, and other stakeholders.

Study Coordination: Coordinate and manage clinical trial activities, ensuring all aspects of the study are conducted in accordance with the protocol, Good Clinical Practice (GCP), and regulatory requirements.
Participant Recruitment and Management: Assist in the recruitment of study participants, screen potential participants for eligibility, and manage participant activities throughout the trial, including consent, enrollment, and follow-up visits.
Data Collection and Management: Collect, record, and maintain research data and documentation with accuracy and integrity. Ensure timely data entry and resolve any discrepancies.
Compliance and Quality Control: Monitor study activities to ensure compliance with protocols and all applicable regulations. Conduct quality control checks to ensure data integrity and protocol adherence.
Communication: Serve as a primary point of contact for the research team, participants, and other stakeholders. Communicate study requirements effectively and provide updates on study progress.
Adverse Event Reporting: Monitor and report adverse events and protocol deviations in a timely manner to the investigator and relevant regulatory bodies.
Study Documentation: Maintain comprehensive records of study activities, including participant files, consent forms, and regulatory documents.
Logistics and Administration: Assist with study logistics, including scheduling appointments, preparing study materials, and organizing meetings.

Education: Bachelor’s degree in a life sciences or healthcare-related field. Relevant certifications, such as Certified Clinical Research Coordinator (CCRC), are advantageous.
Experience: Previous experience in clinical research or healthcare is preferred, demonstrating familiarity with clinical trials and regulatory requirements.
Skills: Excellent organizational, communication, and interpersonal skills; proficiency in data management and electronic data capture systems; attention to detail; ability to multitask.

Detail-Oriented and Organized: Strong attention to detail and organizational skills to manage complex study requirements and maintain meticulous records.
Ethical and Responsible: A strong ethical foundation to ensure participant welfare and adherence to research ethics and patient confidentiality.
Adaptable and Proactive: Ability to adapt to changes in study protocols or regulations and proactively address potential issues in study execution.
Team Player with Strong Communication Skills: Effective communication skills to collaborate with the research team, participants, and other stakeholders, fostering a positive and productive working environment.

Gandhinagar Job ID: 100357622

Your Role *

Your Name *

Your Mobile Number (10 digits) *

Your Email

Job City *

Your Experience *

Your Present Salary *

Captcha :
What is 8 + 5? *

Submit only once

Free registration • Verified hospital jobs • Your details remain confidential

Clinical Research Coordinators (CRCs)