IQVIA Hiring Associate Clinical Trial Manager

IQVIA, a global leader in clinical trials and healthcare insights, is seeking qualified candidates for the role of Associate Clinical Trial Manager in Thane, Maharashtra. If you have a background in healthcare, scientific disciplines, and clinical research experience, this position offers an excellent opportunity to contribute to groundbreaking medical treatments.

About the Role: Associate Clinical Trial Manager

As an Associate Clinical Trial Manager at IQVIA, you will play a critical role in the delivery of clinical trials. You will work alongside clinical teams to bring new drugs to the market efficiently, helping improve patient outcomes. This role is integral to the success of clinical projects and involves the oversight of project operations, quality management, and compliance with regulatory standards.

Key Responsibilities:

•  Ensure clinical delivery of assigned projects in compliance with regulatory requirements (International Conference on Harmonization (ICH)-Good Clinical Practice (GCP), protocol), customer requirements (contract), and internal requirements (policies, Standard Operating Procedures (SOPs), project plans).
• Accountable for meeting projects’ recruitment targets and ensuring appropriate recruitment strategies are in place.
• Contribute to the development of the project risk mitigation plan and manage clinical risks throughout the project’s lifecycle.
• Ensure clinical quality delivery by identifying quality standards/requirements, planning how compliance will be measured, monitoring and overseeing management of clinical quality issues.
• Manage clinical aspects of Project Finances including Estimate at Completion (EAC). Understand the scope of clinical delivery and create plans to deliver. Monitor and manage changes against baseline Estimate at Completion (EAC) and identify additional service opportunities or out of scope work.
• Identify clinical stakeholder landscape for the project and manage both internal and external stakeholders through effective communication and resolution management.
• Collaborate with the clinical team to support milestone achievements. Report to internal and external stakeholders as per project scope requirements.
• Resourcing and Talent Planning of the clinical team. Manage the clinical team at project level to successfully deliver the project through the establishment of high-quality operational plans and guidance and project related trainings.
• Conduct regular team meetings and communicate appropriately to achieve objectives.
• Support professional development by providing feedback to clinical team line managers on performance relative to project tasks.
• May work as the sole Clinical Lead on projects with 1-2 service lines and single/few countries or alongside more senior Clinical Leads to deliver large, global trials.;
• May attend site visits as applicable in support of project delivery.

Qualifications Required

To qualify for the Associate Clinical Trial Manager position, candidates must possess the following:

• Bachelor’s Degree Bachelor’s Degree in health care or other scientific discipline required
• Requires 3 years clinical research/monitoring experience or equivalent combination of education, training and experience.;
• Requires good knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.;
• Requires broad protocol knowledge and therapeutic knowledge.;
• Requires good understanding of Clinical Research industry (drug/device/technology/etc.) and the relevant environments in which it operates.
• Requires basic understanding of project finances.;
• Knowledge of clinical trials – Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e., International Conference on Harmonization (ICH) and Good Clinical Practice (GCP) and relevant local laws, regulations and guidelines, towards clinical trial conduct.;
• Communication – Strong written and verbal communication skills including good command of English language.
• Problem solving – Problem solving skills.
• Organization – Planning, time management and prioritization skills.
• Prioritization – Ability to handle conflicting priorities.
• Quality – Attention to detail and accuracy in work.
• Results-oriented approach to work delivery and output.; and PowerPoint.;
• IT skills – Good software and computer skills, including Microsoft Office applications including but not limited to Microsoft Word, Excel and PowerPoint.;
• Collaboration – Ability to establish and maintain effective working relationships with coworkers, managers and clients.
• Cross-collaboration – Ability to work across cultures and geographies with a high awareness and understanding of cultural differences.
• Effective communication – Ability to influence without authority.
• IQVIA Core Competencies – Ability to demonstrate all IQVIA competencies (Client Focus, Collaboration, Communication, innovation, Ownership).

Location and Work Environment

This position is based in Thane, Maharashtra, offering a dynamic and collaborative environment where you will work with cross-functional teams to drive clinical trial success. IQVIA’s offices provide an atmosphere conducive to professional development, and the role may require occasional site visits.

How to Apply

To apply for the Associate Clinical Trial Manager position at IQVIA, visit the official IQVIA careers page o

Tagged as: Good Clinical Practice (GCP)