IQVIA
Clinical Lead- CVRM
Durham, North Carolina, United States of America · Part-time
Sponsorship not specified$93k-$233kDetected 8 days ago
GCPProject ManagementBusiness DevelopmentNegotiationExcelClinical TrialsClinical ResearchResearchLeadershipCommunicationCollaborationProblem SolvingTime ManagementMentoringMicrosoft OfficeGxP
About the role
- Participate in bid defense preparations and meetings.
- Req • Requires basic knowledge of Project management practices and terminology.
- Req • Requires understanding of project finances.
Responsibilities
- Contribute to the development of the project risk mitigation plan and manage clinical risks through the project's lifecycle.
- 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.
- 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.
- Support professional development by providing feedback to clinical team line managers on performance relative to project tasks.
- Develop and present Clinical Operation plan in partnership with Business Development and Project Leadership.
- May work as a primary Clinical Lead alongside other Clinical Leads to deliver large, global trials.
Requirements
- Requires basic knowledge of Project management practices and terminology.
- Requires good knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Knowledge of clinical trials.
- Ability to handle conflicting priorities.
- Bachelor's Degree Bachelor's Degree in health care or other scientific discipline required Req
- Requires 5 years clinical research/monitoring experience or equivalent combination of education, training and experience. Req
- Requires basic knowledge of Project management practices and terminology. Req
- 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. Req
- Requires understanding of project finances. Req
- Knowledge of clinical trials - Knowledge of clinical trial conduct in addition to 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.
Compensation
- The potential base pay range for this role, when annualized, is $93,100.00 - $232,800.00.
This listing is sourced directly from IQVIA's careers page and normalized into a canonical job model.