Clinical Trial Lead
Cary, NC · On-site +1
... contract, budget, timelinesand withquality. Responsibilities As an expert in Clinical Trial ... Operations. Requirements To be successful you will possess: * A degree in life sciences or nursing ...
Clinical Trial Lead
Cary, NC · On-site +1
... contract, budget, timelinesand withquality. Responsibilities As an expert in Clinical Trial ... Operations. Requirements To be successful you will possess: * A degree in life sciences or nursing ...
Clinical Trial Lead
Cary, NC · Remote
... contract, budget, timelines and with quality. Responsibilities As an expert in Clinical Trial ... Operations. Requirements To be successful you will possess: * A degree in life sciences or nursing ...
Quick apply
Clinical Trial Lead
Cary, NC · Remote
... contract, budget, timelines and with quality. Responsibilities As an expert in Clinical Trial ... Operations. Requirements To be successful you will possess: * A degree in life sciences or nursing ...
Clinical Trial Lead
Cary, NC · On-site +1
... contract, budget, timelines and with quality. Responsibilities As an expert in Clinical Trial ... Operations. Requirements To be successful you will possess: * A degree in life sciences or nursing ...
Clinical Trial Lead
Cary, NC · On-site +1
... contract, budget, timelines and with quality. Responsibilities As an expert in Clinical Trial ... Operations. Requirements To be successful you will possess: * A degree in life sciences or nursing ...
Clinical Trial Manager
Raleigh, NC · On-site +1
Manage the day-to-day operations of assigned trials and responsibilities to ensure completion per ... Manage clinical trial budget and associated vendor contracts, including tracking and data in ...
Clinical Trial Manager
Raleigh, NC · On-site +1
Manage the day-to-day operations of assigned trials and responsibilities to ensure completion per ... Manage clinical trial budget and associated vendor contracts, including tracking and data in ...
Manage the day-to-day operations of assigned trials and responsibilities to ensure completion per ... Manage clinical trial budget and associated vendor contracts, including tracking and data in ...
Manage the day-to-day operations of assigned trials and responsibilities to ensure completion per ... Manage clinical trial budget and associated vendor contracts, including tracking and data in ...
Manage the day-to-day operations of assigned trials and responsibilities to ensure completion per ... Manage clinical trial budget and associated vendor contracts, including tracking and data in ...
Quick apply
Manage the day-to-day operations of assigned trials and responsibilities to ensure completion per ... Manage clinical trial budget and associated vendor contracts, including tracking and data in ...
Clinical Project Coordinator
Raleigh, NC · On-site
... Operations Director with preparing data reports for site and Clinical Research Associate (CRA ... clinical contract research organization (CRO) focused on the advancement of treatments for ...
Clinical Project Coordinator
Raleigh, NC · On-site
... Operations Director with preparing data reports for site and Clinical Research Associate (CRA ... clinical contract research organization (CRO) focused on the advancement of treatments for ...
Senior Clinical Research Associate - US
Raleigh, NC · On-site +1
With operations in 40+ countries and 2x the patient reach of the average mid-sized CRO, we enable ... contracts as applicable * Administration of site payments in accordance with relevant project ...
Senior Clinical Research Associate - US
Raleigh, NC · On-site +1
With operations in 40+ countries and 2x the patient reach of the average mid-sized CRO, we enable ... contracts as applicable * Administration of site payments in accordance with relevant project ...
... Operations Director with preparing data reports for site and Clinical Research Associate (CRA ... clinical contract research organization (CRO) focused on the advancement of treatments for ...
... Operations Director with preparing data reports for site and Clinical Research Associate (CRA ... clinical contract research organization (CRO) focused on the advancement of treatments for ...
Clinical Project Coordinator
Raleigh, NC · On-site
... Operations Director with preparing data reports for site and Clinical Research Associate (CRA ... clinical contract research organization (CRO) focused on the advancement of treatments for ...
Clinical Project Coordinator
Raleigh, NC · On-site
... Operations Director with preparing data reports for site and Clinical Research Associate (CRA ... clinical contract research organization (CRO) focused on the advancement of treatments for ...
Senior Clinical Research Associate - US
Durham, NC · On-site +1
With operations in 40+ countries and 2x the patient reach of the average mid-sized CRO, we enable ... contracts as applicable * Administration of site payments in accordance with relevant project ...
Senior Clinical Research Associate - US
Durham, NC · On-site +1
With operations in 40+ countries and 2x the patient reach of the average mid-sized CRO, we enable ... contracts as applicable * Administration of site payments in accordance with relevant project ...
Responsible for posting of fully executed contracts in eFiliA and locally on the Clinical Operations secure drive. * Process foreachstudy,internalapprovalforms andother documents whichare requiredto ...
Responsible for posting of fully executed contracts in eFiliA and locally on the Clinical Operations secure drive. * Process foreachstudy,internalapprovalforms andother documents whichare requiredto ...
Responsible for posting of fully executed contracts in eFiliA and locally on the Clinical Operations secure drive. * Process foreachstudy,internalapprovalforms andother documents whichare requiredto ...
Responsible for posting of fully executed contracts in eFiliA and locally on the Clinical Operations secure drive. * Process foreachstudy,internalapprovalforms andother documents whichare requiredto ...
Grants Payments Data Analyst
Durham, NC · On-site
Work with the Central Planning and Clinical Operations teams to gather current site enrollment and ... Create client-ready forecast deliverables as specified per sponsor contracts * Perform forecast ...
Grants Payments Data Analyst
Durham, NC · On-site
Work with the Central Planning and Clinical Operations teams to gather current site enrollment and ... Create client-ready forecast deliverables as specified per sponsor contracts * Perform forecast ...
Area Vice President, Cancer Service Line Administration - Greater Wake Area
Wake Forest, NC · On-site
$75.40 - $120.65/hr
... contracts to ensure alignment with NSL goals and organizational standards. * Directly manages ... Partners with clinical and academic leaders to ensure clinical operations appropriately support ...
Area Vice President, Cancer Service Line Administration - Greater Wake Area
Wake Forest, NC · On-site
$75.40 - $120.65/hr
... contracts to ensure alignment with NSL goals and organizational standards. * Directly manages ... Partners with clinical and academic leaders to ensure clinical operations appropriately support ...
Site Contract Manager
$86K - $115K/yr
Provide specialist legal, operational and financial contracting support to the Study Teams, as ... Strong understanding of regulated clinical trial environment and knowledge of drug development ...
Site Contract Manager
$86K - $115K/yr
Provide specialist legal, operational and financial contracting support to the Study Teams, as ... Strong understanding of regulated clinical trial environment and knowledge of drug development ...
Site Contract Manager
$86K - $115K/yr
Provide specialist legal, operational and financial contracting support to the Study Teams, as ... Strong understanding of regulated clinical trial environment and knowledge of drug development ...
Site Contract Manager
$86K - $115K/yr
Provide specialist legal, operational and financial contracting support to the Study Teams, as ... Strong understanding of regulated clinical trial environment and knowledge of drug development ...
Site Contract Manager
Durham, NC · On-site
$86K - $115K/yr
Provide specialist legal, operational and financial contracting support to the Study Teams, as ... Strong understanding of regulated clinical trial environment and knowledge of drug development ...
Site Contract Manager
Durham, NC · On-site
$86K - $115K/yr
Provide specialist legal, operational and financial contracting support to the Study Teams, as ... Strong understanding of regulated clinical trial environment and knowledge of drug development ...
... clinical translational and commercialization. The project coordinator will support project managers ... contract administration, research operations, grants administration, or a related field.
... clinical translational and commercialization. The project coordinator will support project managers ... contract administration, research operations, grants administration, or a related field.
... clinical translational and commercialization. The project coordinator will support project managers ... contract administration, research operations, grants administration, or a related field.
... clinical translational and commercialization. The project coordinator will support project managers ... contract administration, research operations, grants administration, or a related field.
Contract Clinical Operations information
See Raleigh, NC salary details
$34K - $47.4K
5% of jobs
$47.4K - $60.8K
8% of jobs
$69.3K is the 25th percentile. Wages below this are outliers.
$60.8K - $74.2K
18% of jobs
The median wage is $86.5K / yr.
$74.2K - $87.6K
20% of jobs
$87.6K - $101K
19% of jobs
$105.3K is the 75th percentile. Wages above this are outliers.
$101K - $114.4K
14% of jobs
$114.4K - $127.7K
8% of jobs
$127.7K - $141.1K
3% of jobs
$141.1K - $154.5K
1% of jobs
$154.5K - $167.9K
2% of jobs
$167.9K - $181.3K
1% of jobs
$34K
$95.3K
$181.3K
How much do contract clinical operations jobs pay per year?
As of Aug 17, 2026, the average yearly pay for contract clinical operations in Raleigh, NC is $95,302.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,500.00 and $110,300.00 per year, depending on experience, location, and employer.
What is contract clinical operations?
Contract Clinical Operations refer to the management and oversight of clinical trials and research activities that are conducted on a contractual basis, often by external vendors or contract research organizations (CROs). Professionals in this role ensure that clinical studies comply with regulatory requirements, timelines, and budgets while maintaining data integrity and participant safety. They coordinate tasks such as site selection, trial initiation, monitoring, and reporting, often acting as a liaison between sponsors and service providers. This role is essential for pharmaceutical, biotechnology, and medical device companies that outsource clinical research to meet project demands efficiently.
What are the key skills and qualifications needed to thrive in contract clinical operations?
To thrive in Contract Clinical Operations, you need expertise in clinical trial management, regulatory compliance, and contract negotiation, often backed by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and knowledge of ICH-GCP guidelines are typically required. Strong organizational skills, attention to detail, and effective communication help professionals excel in managing multiple stakeholders and timelines. These capabilities ensure clinical studies are executed efficiently, ethically, and in accordance with regulatory standards.
What are some common challenges faced in a contract clinical operations role, and how can they be managed effectively?
Professionals in Contract Clinical Operations often encounter challenges such as coordinating multiple clinical trials across various sites, managing tight timelines, and ensuring strict regulatory compliance. Balancing the needs of sponsors, vendors, and cross-functional teams requires strong communication and organizational skills. Staying proactive, leveraging digital project management tools, and maintaining clear documentation can help address these challenges effectively. Collaborating closely with clinical research associates, data managers, and regulatory specialists is key to ensuring smooth trial execution and problem resolution.
What are the most commonly searched types of Clinical Operations jobs in Raleigh, NC?
The most popular types of Clinical Operations jobs in Raleigh, NC are:
What are popular job titles related to Contract Clinical Operations jobs in Raleigh, NC?
For Contract Clinical Operations jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Contract Clinical Operations jobs in Raleigh, NC look for?
The top searched job categories for Contract Clinical Operations jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Contract Clinical Operations jobs?
Cities near Raleigh, NC with the most Contract Clinical Operations job openings:
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.
ResponsibilitiesAs 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