IQVIA Hiring Clinical Research Associate in Mumbai/Bangalore

IQVIA, a global leader in health information technology and clinical research, is currently seeking qualified candidates for Clinical Research Associate (CRA) roles across various locations in India, including Delhi, Jaipur, Lucknow, and Bangalore. This opportunity is ideal for professionals with 1-4 years of clinical research experience who have dedicated time to CRA responsibilities, actively contributing to the advancement of clinical trials. The role requires candidates with a background in B.Pharm, M.Pharm, or medical qualifications, bringing expertise in oncology, neurology, or biopharmaceuticals.

IQVIA is hiring for CRA roles in India

Clinical Research Associate – I/II

• Job Location: Delhi, Jaipur & Lucknow
• Overall Clinical Research Experience: 1-3years
• CRA Experience Mandatory: 1 year
• Education: B’Pharm/M’Pharm/medically qualified doctors only
• Indication: Any biopharmaceutical

Clinical Research Associate – II

• Job Location: Bangalore
• Overall Clinical Research Experience: 3-4 years
• CRA Experience Mandatory: 2 years
• Indication: Experience in active onsite monitoring of Oncology/Neurology studies for at least 1 year

Job Title: Clinical Research Associate

Experience in Therapeutics: Neurology/Oncology (required)

Job Overview: As a Clinical Research Associate at IQVIA, you will play a vital role in ensuring the smooth conduct of clinical studies. Your responsibilities will include site monitoring, protocol adherence, subject recruitment, and regulatory compliance.

Essential Functions:

•  Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
• Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
• Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
• Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
• Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator’s Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
• Collaborate and liaise with study team members for project execution support as appropriate.
• If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
• If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.

Qualifications:

• Bachelor’s Degree Degree in scientific discipline or health care preferred. Req
• Requires at least 2 years of year of on-site monitoring experience.
• Equivalent combination of education, training and experience may be accepted in lieu of degree.
• Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.
• i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• Good therapeutic and protocol knowledge as provided in company training.
• Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
• Written and verbal communication skills including good command of English language.
• Organizational and problem-solving skills.
• Effective time and financial management skills.
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

How to Apply:

Interested candidates, please Apply through LinkedIn

Tagged as: Good Clinical Practice (GCP), Pharmaceutical Jobs, Pharmacology