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Associate Merck Clinical Trials 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 ... In-depth knowledge of ICH GCP, clinical trials and the critical elements for success in clinical ...

Allucent

Clinical Trial Lead

Cary, NC · Remote

... clinical trials to bring life-changing therapies to patients in need across the globe. We are ... Associates (CRAs) and other clinical functional groups, in their day-to-day clinical trial ...

Parexel

Senior Clinical Research Associate

Raleigh, NC · On-site

Monitor and oversee clinical trials at client sites. Evaluate quality and integrity of reported ... Serving as a Lead Clinical Research Associate (CRA) for clinical studies; Clinical Trial Management ...

Veranex

Sr Clinical Research Associate

Raleigh, NC · On-site

$98K - $140K/yr

Veranex has an exciting opportunity to join our team as a Senior Clinical Research Associate to ... The Sr. CRA will participate in the planning, development, and execution of clinical trials to ...

Allucent

Clinical Trial Lead

Cary, NC · On-site +1

... clinical trials to bring life-changing therapies to patients in need across the globe. We are ... Associates (CRAs) and other clinical functional groups, in their day-to-day clinical trial ...

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Showing results 21-40

All JobsAssociate Merck Clinical Trials JobsAssociate Merck Clinical Trials Jobs in Raleigh, NC

Associate Merck Clinical Trials information

See Raleigh, NC salary details

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How much do associate merck clinical trials jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for associate merck clinical trials 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 is the difference between Associate Merck Clinical Trials vs Clinical Research Coordinator?

AspectAssociate Merck Clinical TrialsClinical Research Coordinator
Required CredentialsBachelor's degree, relevant certifications (e.g., CCRP)Bachelor's degree, often similar certifications
Work EnvironmentPharmaceutical company, clinical trial sites, research labsHospital, research sites, clinics
Employer & IndustryPharmaceutical industry, biotech firmsHealthcare facilities, research organizations
Common Search & ComparisonYesYes

The Associate Merck Clinical Trials role typically involves supporting clinical trial activities within a pharmaceutical company, focusing on drug development and regulatory compliance. In contrast, a Clinical Research Coordinator manages patient recruitment, data collection, and trial logistics at research sites. Both roles require similar educational backgrounds and certifications, but their work environments and specific responsibilities differ, with the Associate Merck Clinical Trials position being more industry-focused and the Clinical Research Coordinator more patient-facing.

What are the most commonly searched types of Merck Clinical Trials jobs in Raleigh, NC?

The most popular types of Merck Clinical Trials jobs in Raleigh, NC are:

What are popular job titles related to Associate Merck Clinical Trials jobs in Raleigh, NC?

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

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The top searched job categories for Associate Merck Clinical Trials jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Associate Merck Clinical Trials jobs?

Cities near Raleigh, NC with the most Associate Merck Clinical Trials job openings:

Associate Merck Clinical Trials jobs near you
Infographic showing various Associate Merck Clinical Trials job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 70% Full Time, 26% Part Time, 1% Temporary, and 2% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $80,847 per year, or $38.9 per hour.

Clinical Trial Lead

Allucent

Cary, NC • On-site, Remote

Full-time

Re-posted 10 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 CTL is responsible for coordinating and managing the planning, implementation, tracking, and ensuring the clinical deliverables as per the trial contract, budget, timelines and with quality.
Responsibilities
As an expert in Clinical Trial Leadership, you are:
  • Coordinating and managing CRA activities across all geographies, liaising with sponsor and Project Manager and other functional leads to ensure clinical monitoring deliverables (timeline, budget, quality, productivity) are met.
  • Liaising closely with the Project Manager (PM) and other department leaders if /when necessary, on all trial-related issues and service delivery.
  • Supporting the management team with training, process improvements, co-monitoring visits, mentoring of staff and / 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 not required.
  • A minimum of 5 years of clinical research experience with at least 2-years' CTL or other relevant experience.
  • In-depth knowledge of ICH GCP, clinical trials and the critical elements for success in clinical trials
  • Strong therapeutic background in oncology
  • Possesses experience and knowledge in the CRO industry that will support Allucent's management 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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