6.0 - 16.0 years

14 - 43 Lacs

Ahmedabad, Gujarat, India

On-site

Description We are seeking an experienced Clinical Trials professional to manage and oversee clinical research studies in India. The ideal candidate will have a strong background in clinical trial design and execution, ensuring compliance with regulatory standards and the safety of trial participants. Responsibilities Design and implement clinical trial protocols in compliance with regulatory standards. Monitor trial progress and ensure adherence to timelines and budgets. Coordinate with various stakeholders, including sponsors, regulatory authorities, and clinical sites. Collect, analyze, and interpret data from clinical trials. Prepare and submit regulatory documents and reports. Train and supervise clinical trial staff and investigators. Ensure the safety and well-being of trial participants. Skills and Qualifications 6-16 years of experience in clinical trials or related field. Strong understanding of Good Clinical Practice (GCP) and regulatory requirements. Proficiency in clinical trial management software and electronic data capture systems. Excellent organizational and project management skills. Strong analytical and problem-solving abilities. Effective communication and interpersonal skills. Ability to work collaboratively in a team environment.

Posted 4 days ago

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Clinical Research Associate Pharma Bharat

0.0 - 3.0 years

0 Lacs

karnataka

On-site

Pharmabharat is a CRO based company specializing in clinical trials with a mission to support and accelerate clinical trials for innovative healthcare solutions. With a team of 11-50 employees, we are headquartered in Maharashtra and belong to the Hospitals and Health Care industry. We are currently looking for a highly motivated Clinical Research Associate to join our team. This full-time position is suitable for freshers with 0 to 1 year of work experience. The job locations include Pune, Bangalore Rural, Hyderabad, and Akrund. The ideal candidate will be responsible for overseeing and supporting clinical trials to ensure compliance with regulatory requirements. Qualifications and Skills: - Minimum of a bachelor's degree in life sciences, health sciences, or a related field. - Strong understanding of clinical trials management (Mandatory skill). - Demonstrated knowledge of regulatory compliance (Mandatory skill). - Proficient in Good Clinical Practice (GCP) guidelines (Mandatory skill). - Ability to analyze complex data and generate reports. - Familiarity with medical terminology. - Strong skills in patient recruitment and retention strategies. - Experience in protocol development and implementation. - Competent in monitoring and auditing clinical trials. Roles and Responsibilities: - Assist in the preparation and implementation of clinical trial protocols. - Monitor and report on the progress of clinical trials. - Ensure compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines. - Recruit and communicate with trial participants. - Collect, analyze, and interpret data from clinical trials. - Conduct site visits and audits to ensure trial integrity. - Maintain accurate documentation and trial records. - Collaborate with cross-functional teams to support trial activities. If you are interested in this opportunity, please visit our website at https://pharmabharat.com/ for more information and to apply for the job.,

Posted 4 days ago

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