Himalaya Pharma Job Vacancy - Clinical Research Associate Post

Himalaya Pharma Job Vacancy – Clinical Research Associate Post

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Job Title: Lead – Clinical Research Associate

From 4 to 8 year(s) of experience

Location: Bangalore/Bengaluru

Eligbility Criteria: 

  • Degree (Graduation or Post Graduation) in science or pharmacy (BSc/BDS/ B.Pharm/ M. Pharm/ M.Sc) with 4-5 years of experience with clinical study monitoring at sponsor or CRO company is preferred.
  • A satisfactory previous experience of monitoring & clinical trial activities
  • Must have thorough knowledge of clinical trial concepts including ICH GCP and relevant regulations for the conduct of clinical trials
  • Fluent in written and spoken English & proficient in MS Office.
  • It may be required for the employee to travel up-to approx. 25- 50%.

Job Description

  • Lead clinical studies to ensure that study is conducted in compliance with the protocol, Sponsors SOPs, Good Clinical Practice (GCP) and relevant regulatory guidelines
  • Perform following monitoring activities directly or mange through SMO/ CRO
  • Perform/ Review/ Oversee Site Identification and conduct Feasibility Studies
  • Perform/ Review/ Oversee Site Selection Visit, Site Initiation Visits, Site Monitoring Visit and Site Closeout Visit
  • Ensure Follow Up letters to sites are sent and submit Visit Reports to the Clinical Project Manager as required
  • Training of study team/ clinical sites on Protocol and other applicable regulatory guidelines including local regulatory guidelines
  • Keep a close association with site (s) for: Patient Recruitment, Patient Follow Up, and protocol related activities along with internal stakeholders
  • Ensure timely Ethics Committee Submission by sites
  • Ensure subject safety and adverse event reporting to sponsor and IRB/IEC
  • Verify drug accountability at sites and at Himalaya and supply/ resupply of study materials
  • Timely CRF retrieval as per the project instructions
    Support the Clinical Project Manager in overall management of the assigned studies.
  • Provide study status updates to team members and project management team and facilitate timely completion of projects
  • Updation of clinical study trackers (including study update/ finance tracking)
  • Maintain accurate and timely sponsor/ CRO/ SMO /site correspondence and communication
  • Primary point of contact for Internal stakeholders including Clinical Project Manager, PMD, DSG, F&D etc.
  • Ensure Central Site Files and Project Management Files are up to date and conduct period review as per SOP/ project requirements
  • Coordination for Archival of study documents (Both in soft copies and hard copies).

Apply Online

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