Clinical Research Associate

8 hours ago

Pune, Maharashtra, India Pharmabharat Full time

Company Overview

Pharmabharat is a Contract Research Organization (CRO) dedicated to assisting in clinical trials. The company operates within the hospitals and healthcare industry, employing between 11 to 50 professionals. For more information, please visit our website at pharmabharat.com.

Job Overview

We are seeking a Clinical Research Associate for our operations based in various locations. This is a full-time position ideal for freshers, requiring between 0 to 1 year of work experience. The selected candidate will be involved in a range of activities related to clinical trial management, regulatory compliance, and protocol development.

Key Responsibilities

  • Monitor clinical trials to ensure compliance with regulatory requirements and study protocols.
  • Facilitate communication between research sites and the project management team to ensure seamless study coordination.
  • Coordinate with medical and statistical staff to prepare study material and presentations.
  • Oversee patient recruitment processes, ensuring the recruitment targets are met within deadlines.
  • Collect and review clinical data to ensure accuracy and consistency as per the trial's design.
  • Participate in study site initial, interim, and close-out visit activities, focusing on protocol adherence and patient safety.
  • Prepare and submit detailed reports on trial progress, ensuring transparency and communication among stakeholders.
  • Engage in regular training updates to maintain clinical trial management and good clinical practice standards.

Requirements

  • Clinical trial management - Ability to plan, execute, and manage clinical trials ensuring adherence to outlined protocols and schedules.
  • Regulatory compliance - Ensuring all clinical trial operations and practices comply with local, national, and hospital regulations.
  • Protocol development - Expertise in developing protocols for drug trials, ensuring they align with scientific and regulatory standards.
  • Data collection and analysis - Skillful in collecting, analyzing, and interpreting data related to clinical trial results and findings.
  • Good Clinical Practice (GCP) - Proficient in maintaining the standards for conducting, recording, and reporting clinical trials involving human subjects.
  • Medical terminology - Understanding of medical language crucial for accurately interpreting and discussing clinical trial data.
  • Patient recruitment - Ability to effectively identify, recruit, and engage potential participants for clinical trials.
  • Report writing - Experienced in writing detailed reports to present findings, methodologies, and results of clinical research.

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