CRC VACANCY: Clinical Research Coordinator in myOnsite Healthcare LLC

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Benefits & Perks

  • Health insurance
  • Paid time off
  • Paid sick time

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BenefitsPulled from the full job description

  • Health insurance
  • Paid sick time
  • Paid time off

Full job description

Join the myOnsite Healthcare Team: Revolutionizing Healthcare

myOnsite Healthcare is at the forefront of revolutionizing healthcare by providing diagnostic bio-specimen collections and CRO services across the US and Canada. Our national presence, dedication to quality, and innovative approach have positioned us as leaders in clinical and life sciences industries. We invite you to be part of our dynamic team as a Clinical Research Coordinator (CRC) in Vadodara, India.

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Position Overview:

The CRC is a critical member of our clinical research team, responsible for supporting the planning, implementation, and management of clinical trials and research studies. Working in the US shift, you will ensure the highest ethical standards, regulatory compliance, and participant safety throughout the research process.

Key Responsibilities:

  • Study Planning and Setup:
  • Collaborate with CRO clients and research teams to design SOPs.
  • Assist in preparing study-related documentation.
  • Coordinate logistics for study initiation meetings.

Study Conduct:

  • Schedule and coordinate participant visits.
  • Collect accurate data and maintain study records.
  • Monitor participant safety and report adverse events.

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Data Management:

  • Conduct regular data quality checks.
  • Ensure data security, confidentiality, and compliance.

Regulatory Compliance and Ethics:

  • Assist in preparing and submitting regulatory documents.
  • Ensure compliance with GCP guidelines and regulations.
  • Facilitate site visits and audits.

Communication and Collaboration:

  • Serve as a primary point of contact for CROs.
  • Foster effective communication within the team.
  • Provide regular updates on study progress.

Administrative Tasks:

  • Coordinate and manage study-related administrative tasks.
  • Assist in preparing and maintaining study-related documentation.

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Qualifications:

  • Bachelor’s degree in a relevant field.
  • Previous experience in clinical research coordination preferred.
  • Strong organizational skills and ability to multitask.
  • Excellent interpersonal and communication skills.
  • Proficiency in electronic data capture systems and Microsoft Office Suite.

Working Conditions:

The role may require occasional flexibility in work hours and collaboration with cross-functional teams. Occasional travel to the US for conferences and customer meetings.

Reporting to Management:

  • Weekly, Monthly, Quarterly, and Yearly Reporting.

Key Performance Indicators (KPIs) with Targets:

  • Participant Enrollment Rate, Data Quality Rate, Participant Retention Rate, Protocol Adherence, Timely Reporting.

Daily Checklist for Daily Follow-Up:

  • Participant Visits, Data Collection, Participant Communication, Study Supplies, Protocol Adherence, Collaboration.

Benefits:

Joining myOnsite Healthcare means becoming part of a global environment. We offer competitive salary, health benefits, growth opportunities, and travel to the US.

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Job Type: Full-time

Benefits:

  • Health insurance
  • Paid sick time
  • Paid time off

Schedule:

  • Night shift
  • US shift

Supplemental pay types:

  • Performance bonus
  • Quarterly bonus

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