Clinical Research Associate

Mediclin Clinical Research

Vasai

On-site

INR 500,000 - 900,000

Full time

3 days ago
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Job summary

Mediclin Clinical Research is seeking a Clinical Research Monitor to conduct site visits and monitor clinical trials in compliance with regulatory requirements. You will collaborate with investigators, clinicians, and other stakeholders to achieve study objectives.

You will develop relationships with sponsors, vendors, and regulatory agencies; coordinate logistics of trials; ensure timely reporting of study data; and participate in quality assurance activities to deliver high-quality

Qualifications

  • Collaborate with investigators, clinicians, and other stakeholders to achieve study objectives.
  • Coordinate and manage the logistics of clinical trials, including equipment, supplies, and personnel.
  • Ensure timely and accurate reporting of study data and progress.
  • Participate in quality assurance activities to ensure high-quality deliverables.

Responsibilities

  • Conduct site visits and monitor clinical trials to ensure compliance with regulatory requirements.
  • Collaborate with investigators, clinicians, and other stakeholders to achieve study objectives.
  • Develop and maintain relationships with key stakeholders, including sponsors, vendors, and regulatory agencies.
  • Coordinate and manage the logistics of clinical trials, including equipment, supplies, and personnel.
  • Ensure timely and accurate reporting of study data and progress.
  • Participate in quality assurance activities to ensure high-quality deliverables.

Job description

  • Conduct site visits and monitor clinical trials to ensure compliance with regulatory requirements.
  • Collaborate with investigators, clinicians, and other stakeholders to achieve study objectives.
  • Develop and maintain relationships with key stakeholders, including sponsors, vendors, and regulatory agencies.
  • Coordinate and manage the logistics of clinical trials, including equipment, supplies, and personnel.
  • Ensure timely and accurate reporting of study data and progress.
  • Participate in quality assurance activities to ensure high-quality deliverables.
Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.
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