Clinical Research Associate

2 months ago

Pune, India Pharmabharat Full time

Company Overview

Pharmabharat is a CRO-based company dedicated to assisting in clinical trials, with its headquarters located in Maharashtra. Operating within the hospitals and health care industry, Pharmabharat is a small enterprise 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 Pune Division, Hyderabad, and Bangalore Urban. 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.


Qualifications and Skills

  • Clinical trial management (Mandatory skill) - Ability to plan, execute, and manage clinical trials ensuring adherence to outlined protocols and schedules.
  • Regulatory compliance (Mandatory skill) - Ensuring all clinical trial operations and practices comply with local, national, and hospital regulations.
  • Protocol development (Mandatory skill) - 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.


Roles and 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.

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