Fortrea

Fortrea

Sr. Manager, Clinical Operations / Madison, WI (On-Site)

Madison · Senior · Part-time

Sponsorship not specified$10k-$15kDetected 97 days ago
GCPCompliancePerformance ManagementClinical TrialsClinical ResearchMedical DevicesResearchLeadershipCommunicationMentoring

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odds of building a lasting career here

37Risky
Cap-exempt (no lottery)0
Sponsors this role80
Entry-level history0
PERM / green-card track0
Lottery odds (Level I)39
Fits your clock70

Thin sponsorship signal and lottery-bound (~15% per draw). A low-probability bet with your clock running. Prioritize cap-exempt roles and proven entry-level sponsors first.

Lottery odds assume a STEM candidate.

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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

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About the role

  • Manager, Clinical Operations, to interact directly with our healthy volunteer participants while learning to read clinical research protocols and enjoy working in a fast-paced team-oriented environment.
  • If you join us, you will work with some of the world´s leading pharmaceutical, biotechnology, and medical device companies in a vital stage of clinical development: establishing the safety, tolerability and pharmacokinetics of a new drug.

Responsibilities

  • Manage the scheduling of resource requirements for all teams under their remit ensuring staff are utilized as efficiently as possible and ensure the safety of volunteers at all times.
  • If scope includes overseeing the Processing Laboratory: Manage the Processing Laboratory and sample dispatch process, ensuring staff are utilized as efficiently as possible and ensuring client requirements are delivered accurately and on time.
  • Manages the security of buildings, staff and visitors in line with Fortrea policy.

Requirements

  • Ability to work in an upright and /or stationary position for 6-8 hours per day.
  • Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists to operate lab equipment.
  • Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
  • Varied hours may be required.

Nice to have

  • Many are drawn to this profession because of its direct impact on patient care.
  • If this is your case, you will not miss that working in Phase 1 trials.
  • When the drug you worked with gets approved, you know you´ll touch many patient´s lives around the world.

Compensation

  • Assist the Senior Clinic Director to compile and implement the Annual P&L for the business unit.
  • Manage the annual business unit capital budget and capital expenditure request (CER) process.

Benefits

  • Support the Senior Clinic Director in the communication of the Fortrea vision to all staff by articulating the goals and objectives of the company in the appropriate format.

Equal opportunity

  • Learn more about our EEO & Accommodations request here.

This listing is sourced directly from Fortrea's careers page and normalized into a canonical job model.