Clinical Research Specialist, Senior - Confidential Client
The Clinical Research Specialist, Senior at Confidential Client supports oncology clinical trials by managing clinical research data, maintaining study documentation, and ensuring compliance with protocols and regulatory standards. This entry-level role involves collaboration with multidisciplinary teams to facilitate participant activities, process research specimens, and uphold ethical research conduct, contributing to innovative cancer research and improved patient outcomes.
About Careertakes
👉 Important disclosure: Careertakes is a third-party recruiting platform supporting this hiring process. If selected, you will be employed directly by our client, Scientific & QA.
Applicants for this role may also receive access to additional matched opportunities through the Careertakes platform.
Minimum Qualifications
Confidential Client is seeking an entry-level Clinical Research Specialist, Senior to support oncology clinical trials. Candidates should meet the minimum qualifications below:
- Associate's degree
- One year of relevant experience (completion of the DOCR North Carolina State Approved Clinical Research Pre-Apprenticeship Program may substitute for the required experience)
- Strong organizational and time management skills
- Critical thinking and problem-solving abilities
- Ability to accurately manage and document clinical research data
- Effective verbal and written communication skills
Preferred Qualifications
- Bachelor’s degree strongly preferred
- Previous experience supporting clinical research studies or clinical trials
- Experience with Electronic Data Capture systems and electronic Case Report Forms (EDC, eCRFs)
- Familiarity with Good Clinical Practice, FDA regulations, and human subject protection requirements
- Experience in oncology research or an academic medical center environment
- Demonstrated attention to detail and commitment to data quality
What You’ll Do
As a Clinical Research Specialist, Senior you will support the Oncology Clinical Research Unit by performing duties such as:
- Manage clinical research data activities, including data entry, review, validation, and maintenance in EDC systems while ensuring accuracy, completeness, security, and regulatory compliance
- Complete and maintain study documentation, including paper and electronic Case Report Forms, source documentation, study files, participant records, and regulatory documents per protocol and SOPs
- Support participant research activities by screening for eligible studies, facilitating consent activities for minimal-risk protocols, scheduling study visits, preparing study materials, and maintaining participant records
- Monitor and resolve data discrepancies by investigating incomplete or missing information and coordinating with study teams to implement quality assurance procedures
- Process and manage research specimens by collecting, preparing, shipping, tracking, and maintaining specimen inventories per protocol and laboratory standards
- Collaborate with multidisciplinary teams including investigators, clinical research staff, sponsors, and regulatory personnel to support protocol implementation and routine study operations
- Promote ethical research conduct by adhering to federal regulations, institutional policies, Good Clinical Practice, and human subject protection standards
- Contribute to continuous improvement efforts through participation in team meetings, training, and quality initiatives
Other Requirements & Working Conditions
- Maintain required training, certifications, and research compliance requirements
- Ability to handle and process biological research specimens per protocol
- This role requires onsite work to support clinical research operations in Durham, NC
- Reasonable accommodations are available for candidates with disabilities; contact the hiring organization for details
Compensation & Benefits
- Base pay range: USD $23.00 to USD $34.50 (hourly range as provided in the source posting)
- Total compensation may include comprehensive medical and dental plans, retirement benefits, and other programs depending on eligibility and the hiring organization
About the Role & Organization
Confidential Client’s Cancer Institute supports a broad portfolio of clinical trials that advance cancer prevention, treatment, and survivorship. This role offers practical experience in oncology clinical research and the opportunity to work with multidisciplinary teams on studies that impact patient care and scientific discovery.
Physical & Accessibility
Certain roles may include essential physical or mental abilities. Reasonable accommodations are available. Applicants may request additional information about essential functions and accommodations from the hiring organization.
Equal Opportunity & Hiring Transparency
Careertakes and our client are Equal Opportunity Employers committed to building a diverse and inclusive workforce. We prohibit discrimination or harassment of any kind. To support a fair and efficient hiring process, AI tools may be used to assist with application review or resume screening. These tools do not replace human decision-making. Final hiring decisions are made by people.
If you have questions about how your data is used, please contact us directly.
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