Clinical Trial Coordinator Fusion Technology Solutions

1.0 - 5.0 years

0 Lacs

ahmedabad, gujarat

On-site

As a Clinical Trial Coordinator, you will be responsible for overseeing the daily activities of clinical trials at various study sites. Your duties will include coordinating patient recruitment, screening, and assisting with the informed consent processes. Additionally, you will be tasked with maintaining trial documentation such as case report forms and regulatory binders. You will play a crucial role in scheduling and tracking study visits, as well as monitoring data collection and entry to ensure accuracy and compliance with protocols. Effective communication with investigators, sponsors, and ethics committees will be essential to the success of the trials. This is a full-time position that offers health insurance benefits. The working hours are during the day shift, and the job requires you to be present in person at the designated work location.,

Posted 2 weeks ago

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Clinical Trial Associate @ Bangalore/Mumbai Contract role Persolkelly India

1.0 - 6.0 years

2 - 6 Lacs

bengaluru, mumbai (all areas)

Work from Office

Role & responsibilities Job Title: Clinical Trial Assistant (CTA) Location: Mumbai Department: Clinical Operations Reports To: Project Manager Job Summary: The CTA will play a crucial role in supporting the clinical team in the preparation, conduct, and administration of clinical trials. This position involves working closely with the Project Manager and other team members to ensure that trials are conducted in compliance with regulatory requirements and company standards. Key Responsibilities: Assist in the preparation and maintenance of essential trial documentation, including trial master files, SIV Kit and regulatory binders. Handling and processing of vendor related agreements/payments Coordinate logistics for trial-related meetings, including scheduling, preparing agendas, and distributing minutes. Support the team in managing trial-related communications with sites, vendors, and internal stakeholders. Assist in tracking trial progress and ensuring adherence to timelines and budgets. Help with the preparation and submission of regulatory and ethics committee applications. Ensure accurate and timely data entry into clinical trial management systems. Assist in the preparation of trial-related reports and presentations. Support the clinical team in resolving issues that arise during the conduct of the trial Tracking budget for the assigned projects Qualifications: Bachelors degree in life sciences, healthcare, or a related field. Previous experience as a CTA for 1 year Strong organizational and time management skills. Excellent communication skills, both written and verbal. Proficiency in Microsoft Office Suite and clinical trial management systems. Ability to work collaboratively in a team-oriented environment. Attention to detail and ability to manage multiple tasks simultaneously. Additional Requirements: Knowledge of Good Clinical Practice (GCP) and regulatory requirements is a plus. Willingness to travel as required. Interested candidate Kindly drop your updated resume to below mail id Nithya_kumar@persolapac.com Regards, Nithya CONFIDENTIAL NOTE: By submitting your resume or personal data, you acknowledge reading and agreeing to our Privacy Policy. You hereby provide voluntary consent to the collection, use, processing, and disclosure of your data by us and our affiliates, in line with the Privacy Policy. and applicable laws. If you wish to withdraw your consent or have any concerns, you may submit a request to our designated consent manager, as outlined in our Privacy Policy. We prioritize your privacy. SECURITY NOTE: We at PERSOLKELLY India or our representatives, do not ask job seekers for fees, personal banking information, or payments through unofficial channels. Official communications will only come from @persolkelly.com. Report any suspicious activity to Contactus_in@persolkelly.com. Click here to find out how you can safeguard yourself from job scams

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