Fortrea
Sr. Clinical Project Manager or Clinical Project Manager II - Ophthalmology
Durham · Senior · Part-time
Sponsorship not specified$125k-$160kDetected 66 days ago
GCPProject ManagementForecastingExcelClinical TrialsClinical ResearchResearchLeadershipCommunicationCollaborationProblem SolvingPublic SpeakingMicrosoft Office
Stay score
odds of building a lasting career here
54Sponsors, lottery-bound
Cap-exempt (no lottery)0
Sponsors this role80
Entry-level history0
PERM / green-card track0
Lottery odds (Level III)83
Fits your clock70
Sponsors, but it's cap-subject — you still face the weighted lottery (~45% per draw at Level III). 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 11 green-card filings in this occupation, 91% were for a worker who already held the job.
Green-card follow-through: 33%
Of 6 labor certifications old enough to have been used, 4 expired without the employer filing the next step. Median time from filing to decision: 489 days.91% 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.
Files H-1B transfers
1 transfer filing in the last year, covering 1 worker. Median labor-condition decision: 7 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
No reports yet — be the first to help the next applicant.
About the role
- A successful Project Manager will bring innovation and future focused approaches to clinical trials with a focus on patient centricity and consistent solutions-oriented delivery.
- % of the above that requires overnight stay: up to 30%
Responsibilities
- Partner with project team members and key stakeholders to oversee and manage project budgets, resources, and scope.
- Develops and mentors team members in multiple areas of expertise and provides feedback as needed to respective line managers.
- Lead the identification of project, financial and quality risk leveraging end to end risk management practices and quality by design principles.
- Appropriately utilize data sources, dashboards, and risk management strategies to drive innovation and proactive problem solving with the project and client teams.
- Lead the adherence to project governance and issue escalation pathways, ensuring that project plans are in place to address identified risk while adhering to professional standards, SOPs, client, and regulatory requirements.
- Project Managers will work to develop and lead high performing teams by collaborating with key stakeholders to manage all aspects of the end-to-end lifecycle of the project including scope, timelines, risk, and budget.
- Demonstrated ability to lead by example and to encourage team members to seek solutions independently.
Requirements
- Experience (Minimum Required):
- Minimum of five (5) years of relevant clinical research experience in a pharmaceutical company/CRO.
- 5 years on clinical project management experience within a CRO or pharma
- Experience in Project Management of the End-to-End Clinical Trial Lifecycle or
- Working knowledge of ICH Guidelines and GCP including international regulatory requirements for the conduct of clinical development programs.
- Experience managing projects in a matrix and virtual environment.
- In collaboration with relevant departments, prepare and deliver presentations for new business as required.
- Weekend and off-hour work as required.
- University/college degree (life science preferred) or certification in a related allied health profession (i.e., nursing, medical or laboratory technology) from an appropriately accredited institution.
- Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
Nice to have
- Master's or other advanced degree.
- PMP certification
- Biotech experience
- What do you get?
- Employee recognition awards
- Multiple ERG's (employee resource groups)
- Applications will be accepted on an ongoing basis.
- Work Environment:
Compensation
- Target Pay Range (based on title): $125-160k
Benefits
- Medical, Dental, Vision, Life, STD/LTD (multiple insurance carriers)
- Paid time off (PTO) - Flex Plan
Equal opportunity
- Learn more about our EEO & Accommodations request here.
Apply directly at Fortrea →Create a free account for alerts like thisView Fortrea immigration profile
This listing is sourced directly from Fortrea's careers page and normalized into a canonical job model.