IQVIA
Sr. Clinical lead
Durham, North Carolina, United States of America · Senior · Part-time
Sponsorship not specified$93k-$233kDetected 3 days ago
GCPProject ManagementBusiness DevelopmentNegotiationExcelClinical TrialsClinical ResearchResearchLeadershipCommunicationCollaborationProblem SolvingTime ManagementMentoringMicrosoft OfficeGxP
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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.
Personalize to your clock →Employer immigration record
from this employer's Department of Labor filings
Green-card filing pattern in this occupation
Context, not a finding about this posting: of this employer's 16 green-card filings in this occupation, 100% were for a worker who already held the job.
Green-card follow-through: 100%
Of 7 labor certifications old enough to have been used, 0 expired without the employer filing the next step. Median time from filing to decision: 493 days.100% of their filings were for a worker who already held the job.Only certifications past the 180-day window are counted — recent ones cannot have expired yet.
Reported a layoff in this occupation
In a green-card filing decided 2026-06-24, this employer stated it had laid off workers in Software Developers (NC) during the preceding six months. 3 such filings on record.Describes the period before that filing, not necessarily today. Unlike WARN notices this is occupation-specific and federal.
DOL often reclassifies their job titles
The Department of Labor assigned a different occupation than this employer requested on 54% of its 28 wage determinations — against a 18% norm. The occupation sets the prevailing wage floor.Reclassification is routine and can reflect genuinely hybrid roles; it is not by itself evidence of underpayment.
Files H-1B transfers
4 transfer filings in the last year, covering 4 workers. Median labor-condition decision: 316 days. An employer that already files transfers is one that can take over an existing H-1B.
Sourced from Department of Labor LCA, PERM and prevailing-wage disclosure data. Employer matching is by name, so figures may be split across an employer's legal entities. Absence of a filing means none appears in our copy of the data, not that none exists.
Community outcomes
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About the role
- Participate in bid defense preparations and meetings.
- Req • Requires consolidated knowledge of Project management practices and terminology.
- Req • Requires understanding of project finances.
Responsibilities
- Manage clinical risks through the project 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.
- Work as the primary Clinical Lead alongside other Clinical Leads to deliver large, global trials.
- 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 to support professional development.
- Develop and present Clinical Operation plan in partnership with Business Development and Project Leadership.
Requirements
- Requires consolidated 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.
- Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements
- Ability to handle conflicting priorities.
- Bachelor's Degree Bachelor's Degree in health care or other scientific discipline required
- Requires 7 years clinical research/monitoring experience or equivalent combination of education, training and experience. Req
- Requires consolidated 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, 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.
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.