Sr Clinical Research Associate iProcess Global Research Inc

2.0 - 6.0 years

0 Lacs

karnataka

On-site

In this role at iProcess, you will be responsible for overseeing biospecimen collection studies across multiple countries. Your key responsibilities will include: - Serving as the primary point of contact for iProcess at specimen collection sites to ensure smooth communication and accurate clinical data transfer. - Facilitating Investigator and Sponsor Meetings, and actively participating in internal and external project meetings. - Managing regulatory documentation for study initiation, monitoring, and evaluation, including obtaining necessary approvals. - Drafting Collection Protocols, Consent Forms, and Case Report Forms (CRFs). - Independently conducting all types of monitoring visits (p...

Posted 2 weeks ago

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Sr Clinical Research Associate iProcess Global Research Inc

2.0 - 6.0 years

0 Lacs

karnataka

On-site

Role Overview As a Senior Clinical Research Associate (CRA) at iProcess, you will be responsible for overseeing biospecimen collection studies across multiple countries. Your main duties will include ensuring compliance with international regulations, maintaining biospecimen integrity, and enforcing adherence to study protocols. Acting as a key liaison between global clinical sites, biorepositories, laboratories, and internal teams, you will play a crucial role in supporting high-quality data and sample collection. Key Responsibilities - Serve as the primary point of contact for iProcess at specimen collection sites, ensuring smooth communication and accurate clinical data transfer. - Facili...

Posted 2 months ago

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