Job highlights

- Experience in conducting site monitoring visits and managing clinical trial data

We are looking for a highly skilled and experienced Clinical Specialist to join our team at IQVIA Biotech. The ideal candidate will have 2-5 years of experience in the field, with proficiency in Punjabi speaking being an added advantage.

Roles and Responsibility

- Collaborate with cross-functional teams to develop and implement clinical trials and studies.

- Conduct site monitoring visits and ensure compliance with regulatory requirements.

- Develop and maintain relationships with investigators, sites, and other stakeholders.

- Provide training and support to site staff on study protocols and procedures.

- Review and approve site documentation, including protocols, case report forms, and investigational reports.

- Ensure timely resolution of site-related issues and queries.

Job Requirements

- Strong knowledge of Valuable Clinical Practice (GCP) principles and regulations.





- Experience in conducting site monitoring visits and managing clinical trial data.

- Excellent communication and interpersonal skills, with the ability to work effectively with diverse stakeholders.

- Ability to work independently and as part of a team, with strong problem-solving and analytical skills.

- Proficiency in using computer systems and software applications, including electronic data capture systems.

- Strong attention to detail and organizational skills, with the ability to prioritize tasks and manage multiple projects simultaneously.

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📌 Clinical Specialist / Stroke Rater Punjabi Speaking (Bengaluru)
🏢 Iqvia Biotech
📍 Bengaluru