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Contract Labcorp Clinical Trials Jobs (NOW HIRING)

University of Alabama at Birmingham

$58 - $94/hr

The Contract Officer will represent the University in negotiating legal terms and conditions of ... Research Organization-Clinical Trials Employee Status Regular Shift : Day/1st Shift Work ...

New

Bausch & Lomb

Senior Manager, Clinical Trials (15543)

OR · On-site +1

Ensure all clinical trials are executed in compliance with international GCP guidelines/regulations ... Develop operating budgets, track expenses, negotiate site/vendor contracts and proactively mitigate ...

ADN Healthcare

Travel Clinical Trials Pharmacist

Boston, MA · On-site

$128K - $153K/yr

This is a Pharmacy position in the Clinical Trials - Non-Oncology(MG7733) (SO00000212 ... Pharmacist,09:00:00-17:00:00 About ADN Healthcare ADN Healthcare has thousands of contract and ...

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Contract Labcorp Clinical Trials information

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$49K

$107.3K

$189K

How much do contract labcorp clinical trials jobs pay per year?

As of Sep 3, 2026, the average yearly pay for contract labcorp clinical trials in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

What is the difference between Contract Labcorp Clinical Trials vs Clinical Research Associate?

AspectContract Labcorp Clinical TrialsClinical Research Associate
CredentialsTypically requires a degree in life sciences, nursing, or related field; certifications like CCRP are commonRequires similar degrees; certifications like CCRP or CRA certification are often preferred
Work EnvironmentContract-based, often in clinical settings or labs, with project-specific durationsUsually in clinical sites or research facilities, monitoring ongoing trials
Employer & IndustryContract labs, pharmaceutical companies, CROsPharmaceutical companies, CROs, research institutions

Contract Labcorp Clinical Trials professionals focus on executing specific clinical trial projects for labs and CROs, often on a contract basis. Clinical Research Associates monitor and manage clinical trials at sites, ensuring compliance and data integrity. While both roles require similar credentials and work in related environments, their responsibilities and employment types differ.

What cities are hiring for Contract Labcorp Clinical Trials jobs?

Cities with the most Contract Labcorp Clinical Trials job openings:

What are the most commonly searched types of Labcorp Clinical Trials jobs?

The most popular types of Labcorp Clinical Trials jobs are:

What states have the most Contract Labcorp Clinical Trials jobs?

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Contract Labcorp Clinical Trials jobs near you

Sr. Clinical Trials Manager

Neurocrine Biosciences, Inc.

San Diego, CA • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

This job post has expired today. Applications are no longer accepted.

Job description

Who We Are:
Neurocrine Biosciences is a leading biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs. We are dedicated to discovering, developing and commercializing life-changing treatments for patients with under-addressed neurological, psychiatric, endocrine and immunological disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, hyperphagia in Prader-Willi syndrome, endometriosis* and uterine fibroids*, as well as a robust pipeline including multiple compounds in mid- to late-phase clinical development across our core therapeutic areas. For more than three decades, we have applied our unique insight into neuroscience and the interconnections between brain and body systems to treat complex conditions. We relentlessly pursue medicines to ease the burden of debilitating diseases and disorders, because you deserve brave science. For more information, visit neurocrine.com, and follow the company on LinkedIn, X, Facebook and YouTube. (*in collaboration with AbbVie)
About the Role:
Contribute to overall clinical trial strategy and responsible for managing the operational activities to support planning, initiation, conduct and close out phases of clinical studies. Leads and manages the end-to-end operational activities of assigned Clinical Studies (domestic and global studies). Manages studies using multiple Contract Research Organizations (CROs) as well as managing internally run studies. Responsible for integrity of clinical trial data and completeness of Trial Master File (TMF) documentation.
Your Contributions (include, but are not limited to):
  • Responsible for developing, leading and managing NBI trials on an end-to-end basis and contribute to the overall trial study strategy and planning
  • Serves as primary point of contact for clinical operations aspects of assigned clinical studies, may oversee other clinical trials assigned to lower level team members
  • Participates, and may lead, in technical and study design discussions and provides expert level counsel and input to clinical trial outlines, protocols, and clinical study reports
  • Manages multiple contract research organizations (CROs) and other contract service providers (CSPs) for assigned studies
  • Oversees study team meetings and manages study issues. Develops and manages study timelines in accordance with corporate goals. Identifies barriers to enrollment and develops recruitment solutions
  • Manages internally run studies (without CROs) including the management of trial monitoring team(s) and develops various study plans, on-site monitoring guidelines, forms, tools and performs onsite monitoring and co-monitoring visits, as necessary
  • Works collaboratively with clinical operations department in developing, implementing and enforcing NBI standard processes across all clinical programs
  • Manages Trial Master File (TMF) content ensuring all study documents are appropriately filed and inspection ready throughout the conduct of the study as well as at study completion
  • Ensures clinical studies are conducted in compliance with Food and Drug Administration (FDA) regulations, EU Directive, International Conference on Harmonization (ICH) guidelines, and NBI Standard Operating Procedures (SOPs) and policies
  • Incorporates Risk Based Monitoring with Clinical Quality Assurance counterparts to assure subject safety and data integrity across NBI Development Programs
  • May support the recruitment, training, management, and career development of subordinates within the clinical operations group
  • Other duties as assigned

Requirements:
  • BS/BA degree AND 8+ years of clinical trial management experience, including CRO/vendor management (domestic and international), monitoring of budget scope, clinical site monitoring or related experience required. OR
  • Master's AND 6+ years of similar experience noted above
  • Expert knowledge of clinical drug development process including working knowledge of ICH, Good Clinical Practices (GCPs), FDA regulations, and EU Directive
  • Excellent knowledge of clinical operations, specifically conducting clinical studies from start-up through close-out and understands clinical development efforts of trials
  • Strong understanding of trial development and extensive trial management protocol and process knowledge across all phases of clinical studies
  • In-depth understanding of Clinical Research industry and the relevant environments in which it operates
  • Ability to identify and organize clinical resources needed to accomplish major projects, set overall trial(s) objectives and provide clear direction to others; expertise planning activities in advance and taking account of possible changing circumstances; manages time effectively
  • Must posses strong presentation and communication skills for internal and external presentations
  • Strong computer skills, organizational skills, interpersonal and team participation skills are essential
  • Anticipates business and industry issues; recommends relevant process / technical / service improvements
  • Demonstrates broad expertise or unique knowledge
  • Considered an expert within the company and may have external presence in area of expertise
  • Applies in-depth expertise in discipline and broad knowledge of other closely related areas to improve efficiency of team
  • Ability to work as part of and lead multiple teams
  • Good leadership, mentoring skills and abilities typically leads lower levels and/or indirect teams
  • Excellent computer skills
  • Excellent communications, problem-solving, analytical thinking skills
  • Sees broader picture and longer-term impact on division/company.
  • Ability to meet multiple deadlines across a variety of projects/programs, with a high degree of accuracy and efficiency
  • Excellent project management, strong project leadership skills
  • Proven ability to work through others to deliver results to the appropriate quality and timeline metrics, monitoring/managing performance and providing feedback; experience productively partnering cross functionally and with customers to advance work effectively and efficiently
  • Proven ability at analyzing data and information to derive conclusions and drive sound decision making
  • Works to improve tools and processes within functional area

#LI-RS1
Neurocrine Biosciences is an EEO/Disability/Vets employer.
We are committed to building a workplace of belonging, respect, and empowerment, and we recognize there are a variety of ways to meet our requirements. We are looking for the best candidate for the job and encourage you to apply even if your experience or qualifications don't line up to exactly what we have outlined in the job description.
The annual base salary we reasonably expect to pay is $156,900.00-$214,000.00. Individual pay decisions depend on various factors, such as primary work location, complexity and responsibility of role, job duties/requirements, and relevant experience and skills. In addition, this position offers an annual bonus with a target of 30% of the earned base salary and eligibility to participate in our equity based long term incentive program. Benefits offered include a retirement savings plan (with company match), paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage in accordance with the terms and conditions of the applicable plans.

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