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Zuventus Healthcare Ltd. Hiring for position of Clinical Research with the following job description:

Qualification: B Pharmacy /M Pharm with 0-5 year experience Location: Mumbai

Responsibilities –

Clinical Research Assistant/Associate -Establish and maintain the tracking tools for assigned

trials. -Create, assemble and coordinate shipping of study materials.

Conduct initial review and tracking of invoices & study payments.

Receive clinical study documents from study team, review for completion, accuracy & expiration, and filling the same in study file.

Preparation of dossier for EC submission and sending the required documents to the sites.
-Prepare the study files (TMF, SMF and ISF) and sending the ISF to the respective sites along with the all required
documents.

Review TMF and SMF inventory for missing and expiring documents on an ongoing basis as per study requirements.

Support maintenance of the Trial Master File (TMF) & Site Master File (SMF) and assist in quality control as appropriate.

Support Clinical Trial manager and CRA to track and file documents and study metrics.
-Review and assist in the collection of essential documents for completeness and compliance with the protocol and appropriate regulations.

Distribute clinical trial related materials to sites or clinical trial team members.

May act as a central contact for designated project communications, correspondence and associated

Support Clinical Trial manager and CRA to track and file documents and study metrics.

Distribute clinical trial related materials to sites or clinical trial team members. -Assist in the creation of study materials, including but not

Updating all the study trackers for updates in timely documentation.

Participate in team meetings and assist in tracking of action items.

Assist CRAS in preparation for clinical trial site monitoring visits. limited to documents, presentations, and reports.

Perform administrative tasks to support Clinical Trial Department and team members as needed.
manners and provide any data as per requirement. Perform in house follow-up of issues and get resolved in timely manner.

Reconciliation and Management of IP and other clinical trial supplies.

Update controlled documents and SOPs as required. -Pharmacovigilance related activities
Clinical Report writing -Product appraisals

Scientific article search and collation of documents -Regulatory documents compilation from medical point of view

Application Process – this Recruitment is completely Resume / CV Selection, Interested candidates share your resume to medico@zuventus.com

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