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Clinical Research Associate IQVIA – Apply Online
IQVIA
Clinical Research Associate II
Bengaluru, Karnataka, India
About the job
Job Title: Clinical Research Associate
Job Location: Bangalore
Therapeutics area experience required: Oncology/Neurology
Job Overview:
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.
Essential Functions:
- Perform site monitoring visits (selection, initiation, monitoring, and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- 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 / ICH 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 the development of the project subject recruitment plan on a per-site basis.
- If applicable, may be accountable for site financial management according to the executed clinical trial agreement and retrieve invoices according to local requirements.
Qualifications:
- Bachelor’s Degree in a scientific discipline or health care preferred.
- Equivalent combination of education, training, and experience may be accepted in lieu of a degree.
- Some organizations require completion of CRA training program or prior monitoring experience.
- Basic 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 Microsoft Word, Excel, PowerPoint, and use of a laptop computer, iPhone, and iPad (where applicable).
- Written and verbal communication skills including a good command of the 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.
Apply now for the position of Clinical Research Associate II at IQVIA in Bengaluru, India. Click here to view the full job posting and submit your application.
