Job title: Clinical Research Associate
Company: Pharmabharat
Job description: Company OverviewPharmabharat 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 .Job OverviewWe 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.
Expected salary: Rs.500000 per year
Location: India
Job date: Sat, 05 Oct 2024 22:35:58 GMT
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