Associate Clinical Lead

Essential Functions : 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 : Bachelor's Degree Bachelor's Degree in health care or other scientific discipline requiredRequires clinical research / monitoring experience or equivalent combination of education, training and experience.

;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.Cross-collaboration - Ability to work across cultures and geographies with a high awareness and understanding of cultural differences.IQVIA is committed to embracing a diverse and inclusive work environment.

Our goal is to attract and retain the best people, regardless of their gender, race, marital status, ethnic origin, national origin, age, disability, sexual orientation, gender identity or any other characteristic.

Join usIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.

We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide .

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