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Contract Clinical Trial Associate Jobs in Raleigh, NC

Allucent

Clinical Trial Lead

Cary, NC · On-site +1

... Associates (CRAs) and other clinical functional groups, in their day-to-day clinical trial ... contract, budget, timelinesand withquality. Responsibilities As an expert in Clinical Trial ...

Allucent

Clinical Trial Lead

Cary, NC · On-site +1

... Associates (CRAs) and other clinical functional groups, in their day-to-day clinical trial ... contract, budget, timelines and with quality. Responsibilities As an expert in Clinical Trial ...

Allucent

Clinical Trial Lead

Cary, NC · Remote

... Associates (CRAs) and other clinical functional groups, in their day-to-day clinical trial ... the trial contract, budget, timelines and with quality. Responsibilities As an expert in ...

IQVIA

Clinical Trial Rater

Durham, NC · Remote

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location: Remote based in the US Hours ... Clinical Specialist Start: immediate Contract based About IQVIA IQVIA is a global leader in ...

IQVIA

Clinical Trial Rater

Raleigh, NC · Remote

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location: Remote based in the US Hours ... Clinical Specialist Start: immediate Contract based About IQVIA IQVIA is a global leader in ...

Belcan

Clinical Study Manager

Durham, NC

$56.99 - $71.32/hr

The Contract Clinical Study Manager provides operational leadership, coordination, and oversight ... Strong knowledge of clinical trial operations, study start-up, maintenance, and close-out ...

TalentBurst, Inc.

Clinical Study Manager

Durham, NC

The Contract Clinical Study Manager provides operational leadership, coordination, and oversight ... Required Knowledge, Skills, and Abilities " Strong knowledge of clinical trial operations, study ...

Belcan

Clinical Study Manager

Durham, NC · On-site

$56.99 - $71.32/hr

The Contract Clinical Study Manager provides operational leadership, coordination, and oversight ... Strong knowledge of clinical trial operations, study start-up, maintenance, and close-out ...

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Contract Clinical Trial Associate information

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How much do contract clinical trial associate jobs pay per hour?

As of Aug 30, 2026, the average hourly pay for contract clinical trial associate in Raleigh, NC is $38.87, according to ZipRecruiter salary data. Most workers in this role earn between $31.30 and $42.74 per hour, depending on experience, location, and employer.

What does a Contract Clinical Trial Associate do?

A Contract Clinical Trial Associate (CTA) supports the planning, coordination, and administration of clinical trials, typically for pharmaceutical or biotechnology companies. Working on a contract basis, they handle tasks such as maintaining trial documentation, assisting with regulatory submissions, coordinating meetings, and ensuring compliance with protocols and guidelines. CTAs play a vital role in helping clinical trials run smoothly by facilitating communication between study sites, sponsors, and regulatory bodies. Their work is crucial in ensuring data integrity and regulatory compliance throughout the trial process.

What are the key skills and qualifications needed to thrive as a Contract Clinical Trial Associate?

To excel as a Contract Clinical Trial Associate, you need foundational knowledge of clinical trial processes, regulatory guidelines (such as GCP and ICH), and a bachelor's degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and regulatory documentation is typically required. Strong organizational skills, attention to detail, and effective communication enable smooth coordination among stakeholders and accurate trial documentation. These competencies are essential to ensure compliance, data integrity, and the successful execution of clinical trials.

What are some common challenges faced by Contract Clinical Trial Associates, and how can they be managed effectively?

Contract Clinical Trial Associates often manage tight deadlines, handle large volumes of documentation, and coordinate with multiple stakeholders across different locations. One key challenge is ensuring compliance with regulatory requirements while maintaining accurate and timely trial records. To manage these challenges, CTAs benefit from strong organizational skills, clear communication, and adaptability in dynamic project environments. Building positive relationships with study teams and proactively addressing issues can also help ensure successful trial support.

What are popular job titles related to Contract Clinical Trial Associate jobs in Raleigh, NC?

For Contract Clinical Trial Associate jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Contract Clinical Trial Associate jobs in Raleigh, NC look for?

The top searched job categories for Contract Clinical Trial Associate jobs in Raleigh, NC are:

Contract Clinical Trial Associate jobs near you
Infographic showing various Contract Clinical Trial Associate job openings in Raleigh, NC as of August 2026, with employment types broken down into 2% As Needed, 78% Full Time, 13% Part Time, and 7% Contract. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $80,847 per year, or $38.9 per hour.

Clinical Trial Lead

Cary, NC • On-site, Remote

Allucent
See more jobs at Allucentexternal

Full-time

Re-posted 15 days ago

Job description

At Allucent, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.

We are looking for a Clinical Trial Leader (CTL) to join our A-team (office-based*/remote). As a CTL at Allucent, you are providing leadership, management and oversight to the Clinical Research Associates (CRAs) and other clinical functional groups, in their day-to-day clinical trial activities on a global, multi-country, or regional basis. The CTLis responsible forcoordinating and managing the planning, implementation, tracking, and ensuring the clinical deliverables as per the trial contract, budget, timelinesand withquality.

Responsibilities

As an expert in Clinical Trial Leadership, you are:

  • Coordinating and managing CRA activities across all geographies, liaising with sponsor and Project Managerand other functional leadsto ensureclinical monitoringdeliverables (timeline, budget, quality, productivity) are met.
  • Liaising closely with the Project Manager (PM) and other department leaders if /whennecessary,on all trial-related issues and service delivery.
  • Supporting the management team with training, process improvements, co-monitoring visits,mentoring ofstaffand /or any other special assignments within Global Clinical Operations.

Requirements

To be successful you will possess:

  • A degree in life sciences or nursing qualification preferred, but notrequired.
  • A minimum of5years ofclinical research experience with at least2-years'CTL or other relevant experience.
  • In-depth knowledge ofICH GCP,clinicaltrialsand the critical elements for success in clinical trials 
  • Strong therapeutic background in oncology
  • Possesses experience and knowledge in the CRO industry that will supportAllucent'smanagement of clinical trials
  • Strong written and verbal communication skills including professional command of English language to communicate with internal and external stakeholders on a daily basis.

Benefits

Benefits of working at Allucent include:

  • Comprehensive benefits package per location
  • Competitive salaries per location
  • Departmental Study/Training Budget for furthering professional development
  • Flexible Working hours (within reason)
  • Opportunity for remote/hybrid* working depending on location
  • Leadership and mentoring opportunities
  • Participation in our Buddy Program as a new or existing employee
  • Internal growth opportunities and career progression
  • Financially rewarding internal employee referral program

Disclaimers:

*Our office-based work policy encourages a dynamic work environment, prescribing a minimum of 2 days in office per week for employees within reasonable distance from one of our global offices.

"The Allucent Talent Acquisition team manages the recruitment and employment process for Allucent (US) LLC and its affiliates (collectively "Allucent"). Allucent does not accept unsolicited resumes from third-party recruiters or uninvited requests for collaboration on any of our open roles. Unsolicited resumes sent to Allucent employees will not obligate Allucent to the future employment of those individuals or potential remuneration to any third-party recruitment agency. Candidates should never be submitted directly to our hiring managers, employees, or human resources."

#LI-Remote #LI-Hybrid #LI-TCW

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