Site Contracts Manager II (Sponsor-Dedicated/ Remote - US only) Syneos HealthSite Contracts Manager II (Sponsor-Dedicated/ Remote - US only)North CarolinaRemoteAs a Site Contracts Manager II, you will serve as a subject matter expert for site budgets and contracts, partnering with investigative sites, academic institutions, sponsors, and cross-functional stakeholders to ensure timely execution of agreements that support clinical trial startup and study conduct. This is an excellent opportunity for an experienced site contracts professional who enjoys balancing contract strategy, budget negotiations, relationship management, and operational execution across multiple therapeutic areas, including oncology.
Account Strategy Director ParexelAccount Strategy DirectorNorth CarolinaLead and coordinate RFP response processes from the sales perspective, partnering with Account Executives, bid defense teams, subject matter experts, and operational teams to develop winning strategies and ensure high-quality, competitive, and timely submissions. Responsibilities include leading proposal strategies, developing customer intelligence, coordinating break-in strategies, and supporting business development initiatives, with opportunities to deepen your expertise and influence account outcomes.
Territory Manager - Research Triangle Park, NC Thea Pharma Inc.Territory Manager - Research Triangle Park, NCResearch Triangle Park, NC$80,000–$145,000 / yearThea Pharma markets a suite of leading eye-care drugs that have been approved by the U.S. Food and Drug Administration (FDA), including ZOLYMBUS, IYUZEH, Zioptan®, Cosopt®, Cosopt® PF, Azasite®, Akten®, and Betimol®, as well as AcellFX Acellular Amniotic Membrane and the portfolio of iVIZIA dry-eye drops and eyelid hygiene products. By focusing its parent company’s passion and expertise within the U.S. market, Thea Pharma’s goal is to deliver uncompromising care that enables all stakeholders to envision the future of ophthalmic treatment with eyes wide open.
Director, Regulatory Affairs CMC ProPharma Group Holdings LLCDirector, Regulatory Affairs CMCRaleigh, NCThe Director, Regulatory Affairs - Chemistry, Manufacturing, and Controls (CMC) is a senior-level contractor role responsible for defining and executing global CMC regulatory strategies across Dyne's development programs, from early-stage development through commercialization and post-approval lifecycle management. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners' most high-profile drug and device programs.
Senior Medical Writer - FSP Parexel International CorpSenior Medical Writer - FSPNCServe as the Medical Writing representative on assigned project teams and demonstrate document leadership: communicate content requirements, coordinate and conduct interdepartmental team review of draft and final documents, schedule and lead/facilitate authoring team meetings to agree on expectations, evaluate progress on tasks, identify issues and facilitate resolutions, manage/drive the timeline, and advance document development to approval, according to Parexel or client guidelines/SOPs. Gather, review, analyze, and evaluate pertinent resources to prepare, develop, and finalize clinical documents for submission to regulatory authorities, including but not limited to: briefing documents, investigator brochures, study protocols, model informed consents, interim and final clinical study reports, common technical document (CTD) clinical overviews and summaries, safety update/aggregate reports, and integrated summaries of safety and efficacy.
NewSenior Patient Recruitment Lead ICON PlcSenior Patient Recruitment LeadRaleigh, NCKey responsibilities include: Developing and executing comprehensive patient recruitment strategies tailored to specific clinical trial objectives, ensuring alignment with study protocols and timelines. Leading cross-functional teams in the identification and engagement of target patient populations, utilizing data-driven insights to optimize recruitment efforts.
NewAssociate Director for Sheps Integrated Research Solutions (SIRS) University of North Carolina at Chapel HillAssociate Director for Sheps Integrated Research Solutions (SIRS)Chapel Hill, NC$115,000–$135,000 / yearDepartment Sheps Ctr for Hlth Serv Res-633100 Career Area Research Professionals Posting Open Date 08/25/2026 Application Deadline 09/24/2026 Open Until Filled No Position Type Permanent Staff (EHRA NF) Working Title Associate Director for Sheps Integrated Research Solutions (SIRS) Appointment Type EHRA Non-Faculty Position Number 20064061 Vacancy ID NF0009978 Full Time/Part Time Full-Time Permanent FTE 1 Hours per week 40 Position Location North Carolina, US Hiring Range $115,000 - $135,000 Proposed Start Date 09/28/2026. University employees can choose from a wide range of professional training opportunities for career growth, skill development and lifelong learning and enjoy exclusive perks for numerous retail, restaurant and performing arts discounts, savings on local child care centers and special rates on select campus events.
Medical Director, Safety Risk Management United Therapeutics CorporationMedical Director, Safety Risk ManagementRaleigh, NCThe Medical Director will contribute clinically and medically to teams, supporting signal detection, aggregate reports, labeling, risk management, and clinical R&D, and lead and drive medical safety strategy in collaboration with other product/program leads & teams for PASS or PAES and Observational Studies. We believe an unlimited supply of tolerable, transplantable organs will eliminate the transplant waiting list and cure end-stage organ diseases for which transplant is not currently an option.
Senior Medical Writer - FSP ParexelSenior Medical Writer - FSPNorth CarolinaServe as the Medical Writing representative on assigned project teams and demonstrate document leadership: communicate content requirements, coordinate and conduct interdepartmental team review of draft and final documents, schedule and lead/facilitate authoring team meetings to agree on expectations, evaluate progress on tasks, identify issues and facilitate resolutions, manage/drive the timeline, and advance document development to approval, according to Parexel or client guidelines/SOPs. Gather, review, analyze, and evaluate pertinent resources to prepare, develop, and finalize clinical documents for submission to regulatory authorities, including but not limited to: briefing documents, investigator brochures, study protocols, model informed consents, interim and final clinical study reports, common technical document (CTD) clinical overviews and summaries, safety update/aggregate reports, and integrated summaries of safety and efficacy.
Medical Science Liaison, Autoimmune CAR-T, VA/NC/SC/GA Novartis AGMedical Science Liaison, Autoimmune CAR-T, VA/NC/SC/GANCRemote$145,600–$270,400 / yearKey responsibilities:The MSL will leverage scientific expertise and market knowledge to establish and build professional relationships and engage with HCPs (including community physicians, pharmacists, medical experts, nurses, and other healthcare professionals) and other thought leaders in geographical area as aligned with medical strategyThe primary responsibility of the MSL is to engage with customers - customer engagements may include but are not limited to: emerging data discussions, clinical trial activities, uncovering barriers in patient journey, understanding market dynamics within their territory, exploration of areas of unmet medical need, pipeline discussions, educating on disease state and product, capturing adverse events, and capturing medical insights through all stages of product lifecycle. Maintain in-depth knowledge of assigned therapeutic area and Novartis compounds to serve as a medical resource to customers and internal colleagues (in accordance with Working Practice Documents).Maintain in-depth knowledge of internal policies and external regulations (e.g., field medical Working Practice Document (WPD), travel policy, expense policy, state and local laws, institutional policies) and how they affect day-to-day responsibilities.
Associate Director / Director, Project Management - Renal diseases - US/Canada - Remote Worldwide Clinical Trials Holdings IncAssociate Director / Director, Project Management - Renal diseases - US/Canada - RemoteNCRemote$128,500–$254,500 / yearUniversity/college degree (life science preferred) or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology) or equivalent combination of education and experience that provides the individual with the required knowledge, skills and abilities. Work effectively across multiple divisions to direct the delivery of projects/programs within cost, time and quality requirements, and ensure successful design, implementation, tracking and revision of project plans for assigned projects.
Director, Image Analysis & RPT Perceptive Informatics LLCDirector, Image Analysis & RPTNC$148,067–$211,523 / yearAs Director, Image Analysis & Radiopharmaceutical Therapy, you will provide integrated scientific and management leadership across imaging-driven clinical trials, providing scientific guidance on development of modelling, analysis design, results interpretation and dosimetry techniques to clinical trials. This role combines scientific leadership and oversight with functional and people management responsibility to ensure consistent, high-quality data delivery, robust methodology, and operational excellence aligned with business objectives and regulatory expectations.
Case Manager GD Information TechnologyCase ManagerFort Bragg, North CarolinaProfessional oral and written communication skills with peers, outside agencies, vendors, providers, and Military Health System (MHS) stakeholders to exchange information, provide briefings, presentations, research, and metrics to demonstrate or advance effective, efficient case management practice, outcomes, and organizational/MHS value. Minimum of two (2) years’ nursing experience or case management and be certified as a case manager by a recognized certifying organization, i.e., Commission for Case Management Certification, American Case Manager Association, or American Nurse Credentialing Center or shall obtain the certification within one (1) year of hiring.
Consultant - Integration Veeva SystemsConsultant - IntegrationRaleigh, NCRemote$70,000–$140,000 / yearUnlike a traditional corporation, whose only legal duty is to maximize shareholder value, PBCs consider their public benefit purpose and the interests of those materially affected by the corporation's conduct-including customers, employees, and the community-in addition to shareholders' interests. In this role, you'll help implement integrations for SiteVault, a solution focused on clinical research sites, and play a key part in ensuring customers' long-term success.
Research Assistant Odyssey Systems Consulting Group, Ltd.Research AssistantFort Bragg, North CarolinaFull timeResponsibilities: Duties include, but are not limited to: Performs data entry for clinical investigation research projects and maintains databases meticulously including recruitment/screening of potential study subjects; data maintenance; scheduling and testing spreadsheets for participant consenting, study evaluations, and follow up study visits. Extracts data from patient and/or research participant medical records; transcribes and resolves data queries in study forms (hardcopy and/or electronic); prepares documents, under direction of project leaders; prepares data for statistical analyses and reports descriptive data to be used in research/clinical investigations/studies reports.
NewStudy Start Up Associate II IREStudy Start Up Associate IICary, North CarolinaThis may include: Oversight of site level SSU activities from receipt of a potential site list to site activation under the direction of a Global SSU Manager including CDA and questionnaire collection, ICF negotiations, IRB/EC submissions, IMP Release and other site activation requirements. This includes effective communication and coordination with key business stakeholders (e.g., study teams) to support timely completion of both drug and non-drug program goals and objectives.
NewResearch Coordinator University of North Carolina at Chapel HillResearch CoordinatorChapel Hill, NC$19–$22 / hourAssist principal investigator in study related activities including but not limited to: recruitment and enrollment of children and their families into research studies; conducting study visits; chart reviews and abstraction of clinical data from the electronic medical record; data collection and data entry; and sample collection and processing. Department UNC Kidney Center - 427601 Career Area Research Professionals Posting Open Date 09/02/2026 Application Deadline 09/05/2026 Position Type Temporary Staff (SHRA) Position Title Research Coordinator Position Number 20078437 Vacancy ID S028032 Full-time/Part-time Full-Time Temporary Hours per week 40 Work Schedule.
NewResearch Specialist-CIND University of North Carolina at Chapel HillResearch Specialist-CINDChapel Hill, NC$22–$28 / hourDepartment CIND -CarolinaInstitute for ND - 429401 Career Area Research Professionals Posting Open Date 09/03/2026 Application Deadline 09/07/2026 Position Type Temporary Staff (SHRA) Position Title Research Specialist-CIND Position Number 20078475 Vacancy ID S028033 Full-time/Part-time Full-Time Temporary Hours per week 40 Work Schedule Position Location North Carolina, US Hiring Range $22.00 - $28.00 per hour Proposed Start Date Estimated Duration of Appointment 6 months or longer. University employees can choose from a wide range of professional training opportunities for career growth, skill development and lifelong learning and enjoy exclusive perks that include numerous retail and restaurant discounts, savings on local child care centers and special rates for performing arts events.
Director, Therapeutic Strategy Lead - Level Dependent on Experience Join The CTI TeamDirector, Therapeutic Strategy Lead - Level Dependent on ExperienceRaleigh, North CarolinaFor competitive bids and pre-award activities, provide input and guidance during requests for information (RFIs), requests for proposals (RFPs), and bid defense process, to help drive strategy and increase CTI win rate Work directly with Clin Ops and BD to provide therapeutic insights in the development of proposal strategies and scenarios to help secure new and repeat business. Involved in the full RFP response process including leading the development of the delivery strategy, contributing text or figures/tables to the deliverable(s), reviewing the CTI budget, engaging with CTI stakeholders across functions, supporting/developing content for bid defense meetings.
REMS Operations & Implementation Lead (Remote - US) MMSREMS Operations & Implementation Lead (Remote - US)Raleigh, NCRemoteThis role is responsible for gathering, analyzing, and translating client requirements into detailed business and functional requirements, while coordinating cross-functional projects to ensure compliant REMS websites and technology solutions are delivered on time, and in accordance with regulatory requirements. The REMS Business Analyst serves as the critical liaison between business stakeholders, sponsors, and IT teams to ensure the successful delivery of Risk Evaluation and Mitigation Strategy (REMS) programs and supporting REMS solutions.