Clinical Lead

hace 5 días


Bogotá, Bogotá D.E., Colombia IQVIA A tiempo completo
About the Role

We are seeking an experienced Clinical Lead to join our team at IQVIA. As a Clinical Lead, you will be responsible for providing leadership of the clinical team, in support of the project leader, and in collaboration with other functional teams, to achieve the delivery of the project's overall objectives to the Sponsor's satisfaction per contract while optimizing speed, quality, and cost of delivery and in accordance with our SOPs, policies, and practices.

Key Responsibilities
  • Participate in Bid Defense Preparations: Attend bid defense presentations and lead the clinical delivery strategy for medium-size and multiple country/region studies, in partnership with business development and senior project leader as needed.
  • Develop and Maintain Clinical Project Plans: Develop and maintain clinical project plans, including but not limited to clinical operations plan, recruitment, and retention strategy plan, etc. to be incorporated into the integrated study management plan/project management plan.
  • Accountable for Clinical Delivery: Accountable for the clinical delivery (subject recruitment, site management, data integrity) per contract, ensuring consistent use of study tools and training materials and compliance with standard processes, policies, and procedures.
  • Partner with Project Leaders: Partner with the project leaders to confirm objectives of the clinical team according to agreed-upon contract, strategy, and approach. Effectively communicate and assess performance against these agreed objectives.
  • Ensure Subject/Patient Recruitment Strategies: Ensure all appropriate subject/patient recruitment strategies are in place at the outset of the study to maximize subject/patient recruitment opportunities to achieve delivery according to contract, including, but not limited to, all outreach or digital offerings being explored and deployed.
Essential Requirements
  • In-Depth Knowledge of Clinical Research Regulatory Requirements: In-depth knowledge of, and skill in applying applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
  • Project Management Practices and Terminology: Knowledge of Project management practices and terminology.
  • Experience in Internal Medicine and/or CVRM Studies: Experience in Internal Medicine and/or CVRM studies (mandatory).
  • Ability to Identify and Organize Clinical Resources: Ability to identify and organize clinical resources needed to accomplish tasks, set objectives, and provide clear direction to others; experience planning activities in advance and taking account of possible changing circumstances.
  • Education and Experience: Bachelor's degree in a health care or other scientific discipline with 7 years clinical research/monitoring experience; or equivalent combination of education, training, and experience.
  • Minimum 4 Years' Experience: At least 4 years' experience in the role.


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