Top 379 Research scientist Jobs in Durham Nc

Clinical Study Manager
Kaztronix —Durham, NC
- Contract
- Office
- Bachelor's degree
- Contracts
Quick Apply
Entry Level Engineers/Scientists/Chemists/Technicians
ERG —Durham, NC
- $50,000 - $60,000 a year
- Online Application
- Bachelor of Science
- CDL
- Analysis skills
- Profit sharing
- Paid holidays
Quick Apply
Molecular Scientist
Battelle —Durham, NC
- $80,000 - $105,000 a year
- Full-time
- Hybrid work
- Bachelor of Science
- Bachelor's degree
- Travel
- Wellness program
- Health insurance
Psychometrician
AICPA-CIMA —Durham, NC
- $80,000 - $95,000 a year
- Email
- Remote
- Analysis skills
- Continuous improvement
- Doctor of Philosophy
- Health insurance
- Paid time off
Bachelor's-level Health Economist - Health Policy
RTI International —Durham, NC
- $60,000 - $70,000 a year
- Full-time
- Remote
- Microsoft Word
- Microsoft Excel
- Computer Science
- Paid parental leave
- Disability insurance
Scientist - Upstream Cell Culture
Novartis —Durham, NC
- $93,800 - $174,200 a year
- Full-time
- English
- Master's degree
- Bachelor's degree
- Health insurance
- 401(k) matching
Clinical Research Associate 2, IQVIA
IQVIA —Durham, NC
- $71,900 - $189,000 a year
- Full-time
- Microsoft Excel
- Computer literacy
- English
Clinical Lab Scientist I
Galaxy Diagnostics, Inc. —Research Triangle Park, NC
- Full-time
- OSHA
- Bachelor of Science
- HIPAA
Quick Apply
Safety Associate
IQVIA —Durham, NC
- $44,900 - $112,100 a year
- Full-time
- Mid-level
- High school diploma or GED
- Travel
- Work from home
4d
Junior Engineers/Scientists/Technicians
ERG —Durham, NC
- $60,000 - $75,000 a year
- Online Application
- Bachelor of Science
- 3 years
- Analysis skills
- Profit sharing
- Paid holidays
Quick Apply
Row Crop Trait Discovery Research Scientist
Pairwise Plant Service, Inc. —Durham, NC
- Full-time
- Doctor of Philosophy
- Organizational skills
- Senior level
- Health savings account
- Disability insurance
11d
Clinical Service Evaluator II (Full-Time Remote, North Carolina Based)
Alliance Health —Morrisville, NC
- $61,439 - $79,871 a year
- Full-time
- Remote
- Microsoft Access
- 5 years
- Mid-level
- Disability insurance
- Health insurance
EDC Clinical Trial Designer
IQVIA —Durham, NC
- $68,500 - $171,100 a year
- Full-time
- Remote
- Customer service
- Bachelor of Science
- Mid-level
- Work from home
Epidemiologist, Virology, Real World Evidence (FSP Sponsor Dedicated)
IQVIA —Durham, NC
- $109,200 - $273,000 a year
- Full-time
- Remote
- 5 years
- Master's degree
- Analysis skills
- Work from home
Research Analyst
Metabolon, Inc. —Morrisville, NC
- Full-time
- Hybrid work
- Mid-level
- Office
- Analysis skills
KBI: US - Research Associate II
KBI Biopharma —Durham, NC
- $63,000 - $80,000 a year
- Full-time
- Mid-level
- Master's degree
- Analysis skills
- Paid holidays
- Health insurance
Master's-level Health Economist - Health Policy
RTI International —Durham, NC
- $74,000 - $90,000 a year
- Microsoft Word
- Microsoft Excel
- Computer Science
- Paid parental leave
- Disability insurance
Clinical Research Associate, Sponsor Dedicated, Oncology
IQVIA —Durham, NC
- $90,200 - $197,500 a year
- Full-time
- Bachelor of Science
- Bachelor's degree
- Communication skills
9d
Study Coordinator
University of North Carolina at Chapel Hill —Chapel Hill, NC
- $62,000 - $72,000 a year
- Full-time
- Mid-level
- Bachelor's degree
- 1 year
- Health insurance
- Retirement plan
12d
Clincal Research Coordinator - Respiratory Therapy
Duke Health —Durham, NC
- Full-time
- Inpatient
- Mid-level
- Outpatient experience

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Clinical Study Manager

Kaztronix -
Durham, NC

Quick Apply

Job Details

Contract

Qualifications

Document control experience within pharmaceutical industry
Clinical trial risk management
ICH guidelines
Managing clinical research teams
Vendor relationship management
Clinical trial standard operating procedures
Productivity software
Clinical quality assurance standards
Research and development project management
Cross-functional collaboration
Cross-functional team management
Standard operating procedures (SOPs)
Cross-functional communication

Full Job Description

Contract Clinical Study Manager
M-F, 1st shift - hybrid - 3 days in office in RTP

The Contract Clinical Study Manager provides operational leadership, coordination, and oversight for assigned clinical studies. This role supports the successful execution of study activities in accordance with ICH/GCP guidelines, applicable regulatory requirements, company SOPs, study protocols, and study-specific plans. The Contract Clinical Study Manager works closely with internal cross-functional teams, CROs, vendors, investigators, and study site personnel to ensure study deliverables are completed with quality, within expected timelines, and in alignment with study objectives.

Primary Responsibilities
" Provide day-to-day study management support and oversight for assigned clinical study activities from start-up through close-out.
" Coordinate with internal project team members, CROs, vendors, investigators, and study coordinators to support milestone achievement and timely delivery of study activities.
" Monitor adherence to essential document collection processes, site activation requirements, clinical supply release requirements, and study-specific tracking tools.
" Support and/or lead meetings with CROs, vendors, and cross-functional teams to review study progress, risks, issues, action items, and deliverables.
" Track and support development of study-specific timelines, deliverables, and mitigation plans to address study delays or operational risks.
" Assist in vendor selection activities, including contribution to RFPs, scopes of work, vendor budgets, and study/vendor-specific planning documents.
" Evaluate CRO and vendor performance and support early identification, escalation, mitigation, and resolution of potential issues.
" Develop, implement, and follow up on corrective and preventive action plans, as appropriate.
" Coordinate and verify study-specific training for CRO staff, vendors, investigators, study coordinators, and other relevant study team members.
" Support oversight of vendor staff qualification, training, turnover documentation, and ongoing performance against study milestones and KPIs.
" Assist in the management and maintenance of the Trial Master File, including accurate filing, reconciliation, ongoing review, and execution of quality control activities.
" Draft, review, and/or approve study-related documents, including informed consent forms, site worksheets, vendor/site manuals, pharmacy manuals, laboratory manuals, monitoring plans, and monitoring reports, as applicable.
" Review and support responses to site audits, monitoring findings, and other escalated study conduct issues.
" Provide clinical and operational responses to study centers, CROs, vendors, IRBs/ECs, and internal stakeholders, escalating issues when appropriate.
" Ensure study documentation supports inspection readiness and compliance with applicable regulatory requirements, company SOPs, and study protocols.
" Oversee CTMS tracking and study status reporting to support evaluation and management of study set-up, conduct, follow-up, and close-out activities.
" Review clinical data, data listings, vendor reports, monitoring trends, and other study outputs to support data integrity and GCP compliance.
" Provide clinical input into case report forms, data management plans, data transfer plans, and clinical data review activities.
" Collaborate with data management, safety, regulatory, clinical supplies, contracts, biostatistics, and other functional groups to support study execution.
" Prepare key reports on study progress, risks, issues, action items, and delegated clinical study management responsibilities.
" Provide input into study, site, and vendor budgets, as needed.
" Review site and vendor invoices to ensure expenses are consistent with work performed, approved budgets, and study agreements.
" Support investigator budget templates, vendor scopes of work, contract-related inputs, and study financial tracking activities.
" Managers and supervisors may assign other duties as needed.

Required Knowledge, Skills, and Abilities
" Strong knowledge of clinical trial operations, study start-up, maintenance, and close-out activities.
" Strong knowledge of ICH/GCP guidelines, applicable regulatory requirements, clinical study protocols, and company SOPs.
" Demonstrated ability to manage CROs, vendors, study timelines, risks, action items, and cross-functional deliverables.
" Ability to identify issues, evaluate options, make sound recommendations, and drive timely resolution.
" Strong verbal, written, organizational, and interpersonal communication skills.
" Ability to manage competing priorities, work independently, and collaborate effectively with internal and external stakeholders.
" Experience using clinical systems and tools such as CTMS, eTMF, EDC, Microsoft Office, and study-specific tracking tools.

Education and Experience
" Bachelor s degree in a life science, health-related, or related field preferred; equivalent directly related experience may be considered.
" At least eight years of clinical research experience, including at least two years of experience in clinical study management, clinical operations, or related clinical trial roles.
" Experience working with CROs, vendors, clinical sites, and cross-functional study teams is required.
" Experience in sponsor-side study management, vendor oversight, TMF management, audit/inspection readiness, and clinical study documentation is preferred.

Quick Apply

Refine Your Search

research scientist jobs in durham nc

Clinical Study Manager

Entry Level Engineers/Scientists/Chemists/Technicians

Molecular Scientist

Psychometrician

Bachelor's-level Health Economist - Health Policy

Scientist - Upstream Cell Culture

Clinical Research Associate 2, IQVIA

Clinical Lab Scientist I

Safety Associate

Junior Engineers/Scientists/Technicians

Row Crop Trait Discovery Research Scientist

Clinical Service Evaluator II (Full-Time Remote, North Carolina Based)

EDC Clinical Trial Designer

Epidemiologist, Virology, Real World Evidence (FSP Sponsor Dedicated)

Research Analyst

KBI: US - Research Associate II

Master's-level Health Economist - Health Policy

Clinical Research Associate, Sponsor Dedicated, Oncology

Study Coordinator

Clincal Research Coordinator - Respiratory Therapy

I want to receive the latest job alert for research scientist in durham nc

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