IQVIA
Clinical Project Manager- Oncology
Durham, North Carolina, United States of America · Part-time
Sponsorship not specified$93k-$233kDetected 1 day ago
GCPProject ManagementBusiness DevelopmentExcelVendor ManagementCustomer SupportClinical TrialsClinical ResearchResearchLeadershipCommunicationCollaborationProblem SolvingTime ManagementPublic SpeakingMicrosoft Office
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odds of building a lasting career here
64Sponsors, lottery-bound
Cap-exempt (no lottery)0
Sponsors this role100
Entry-level history0
PERM / green-card track0
Lottery odds (Level IV)94
Fits your clock70
Sponsors, but it's cap-subject — you still face the weighted lottery (~61% per draw at Level IV). Good if you win; have a cap-exempt backup on your list.
Lottery odds assume a STEM candidate.
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About the role
- Clinical Project Management is focused on project delivery, productivity and quality resulting in strong financial performance and customer satisfaction.
- Broad protocol knowledge; therapeutic knowledge desired.
Responsibilities
- Participate in bid defense presentations in partnership with Business Development and may lead the presentation for smaller, less complex regional studies.
- Develop integrated study management plans with the core project team.
- Collaborate with other functional groups within the company where necessary to support milestone achievement and to manage study issues and obstacles.
- Manage risk (positive and negative) and contingencies proactively and lead problem solving and resolution efforts.
- Identify changes in scope and manage change control process as necessary.
- Identify lessons learned and implement best practices.
- Support staff development and mentor less experienced project team members on assigned projects to support their professional development.;
- Ability to make decisions, bringing clarity to disparate information to inform actions and drive results.
Requirements
- Bachelor's Degree Life sciences or related field Req
- Knowledge of clinical trials.
- Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e. ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct.
- Ability to organize 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.
- Ability to handle conflicting priorities.
- Ability to work across geographies displaying high awareness and understanding of cultural differences.
- Ability to demonstrate all IQVIA competencies (Client Focus, Collaboration, Communication, innovation, Ownership).
- All information and credentials submitted in your application must be truthful and complete.
Compensation
- The potential base pay range for this role, when annualized, is $93,100.00 - $232,800.00.
Benefits
- 5 years of prior relevant experience including > 1 years project management experience or equivalent combination of education, training and experience. Req
This listing is sourced directly from IQVIA's careers page and normalized into a canonical job model.