Top 77 Clinical study manager Jobs in Durham Nc

Start-up Team Manager (STM) - FSP
Thermo Fisher Scientific —North Carolina
- Weekends as needed
- Remote
- Mid-level
- Clinic
- Bachelor's degree
- Health insurance
3d
Manager, Clinical Operations
IQVIA —Durham, NC
- $86,500 - $216,000 a year
- Full-time
- Remote
- Microsoft Excel
- English
- Mid-level
- Work from home
Senior Clinical Trial Manager - Metabolic
Worldwide Clinical Trials —Research Triangle Park, NC
- $112,000 - $222,000 a year
- Full-time
- Nursing
- English
- Bachelor's degree
12d
Clinical Project Manager- IVD
IQVIA —Durham, NC
- $93,100 - $232,800 a year
- Full-time
- Remote
- Bachelor's degree
- 1 year
- Senior level
- Work from home
RWE Clinical Project Manager (FSP)
IQVIA —Durham, NC
- $93,100 - $232,800 a year
- Full-time
- Remote
- Mid-level
- Bachelor's degree
- Continuous improvement
- Work from home
Manager, Site Contracts with Clinical Trials experience Hybrid or Remote in USA-NC
Syneos - Clinical and Corporate - Prod —Morrisville, NC
- $79,800 - $139,600 a year
- Full-time
- Remote
- Nursing
- Bachelor's degree
- Continuous improvement
- Employee stock purchase plan
- Health insurance
Clinical Program Manager
bioventus —Durham, NC
- Full-time
- Anatomy knowledge
- Bachelor of Science
- Master's degree
7d
Clinical Study Design Manager
Science 37 —Raleigh, NC
- Remote
- Mid-level
- Analysis skills
- Bachelor's degree
Quick Apply
(Senior) Clinical Study Manager, Clinical Development
Tempus —Research Triangle Park, NC
- $100,000 - $140,000 a year
- Full-time
- Nursing
- 5 years
- HIPAA
- Health insurance
Clinical Project Manager
IQVIA —Durham, NC
- $93,100 - $232,800 a year
- Full-time
- Remote
- Microsoft Excel
- Customer service
- English
- Work from home
11d
Senior Clinical Trial Manager - Oncology
Worldwide Clinical Trials —Durham, NC
- $112,000 - $222,000 a year
- Full-time
- Nursing
- English
- Bachelor's degree
4d
Manager, Site Contracts with Clinical Trials experience Hybrid or Remote in USA-NC
サイネオス・ヘルス —Morrisville, NC
- $79,800 - $139,600 a year
- Remote
- Nursing
- Bachelor's degree
- Continuous improvement
- Employee stock purchase plan
- Health insurance
Clinical Lead- CVRM/MASH
IQVIA —Durham, NC
- $93,100 - $232,800 a year
- Full-time
- Remote
- Microsoft Excel
- 5 years
- English
- Work from home
Clinical Project Manager Director (MASH)
IQVIA —Durham, NC
- $125,900 - $350,900 a year
- Full-time
- Remote
- Microsoft Excel
- English
- 8 years
- Work from home
5d
Senior Clinical Project Manager, Immuno-Oncology, IQVIA Biotech
IQVIA —Durham, NC
- $93,100 - $232,800 a year
- Full-time
- Remote
- 7 years
- Microsoft Office
- Bachelor's degree
- Work from home
Associate Clinical Lead Director
IQVIA —Durham, NC
- $102,500 - $285,500 a year
- Full-time
- Remote
- Microsoft Excel
- English
- Bachelor's degree
- Work from home
Associate Manager / Manager, Project Services - Laboratories (Remote - East Coast)
IQVIA —Durham, NC
- $64,200 - $173,000 a year
- Full-time
- Remote
- Microsoft Excel
- Computer literacy
- Data analysis skills
- Work from home
Senior Global Clinical Study Manager
IQVIA —Durham, NC
- $93,100 - $232,800 a year
- Full-time
- Remote
- Bachelor's degree
- Continuous improvement
- Mentoring
- Work from home
Global Study Associate Director
AstraZeneca —Durham, NC
- $137,937.60 - $206,906.40 a year
- Office
- Master's degree
- Bachelor's degree
- Health insurance
- Dental insurance
10d
Site Activation Manager
IQVIA —Durham, NC
- $86,500 - $216,000 a year
- Full-time
- Remote
- Bachelor's degree
- Team management
- Mentoring
- Work from home

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Start-up Team Manager (STM) - FSP

Thermo Fisher Scientific -
North Carolina

Apply Now

Job Details

Full-time
3 days ago

Benefits

Health insurance

Qualifications

Project team coordination
Project reporting
Research project management
Project development phase management
Customer relationship building
Managing healthcare project budgets
Regulatory compliance
Operations coordination planning
Contract performance monitoring
Metrics Reporting
Mid-level
Client relationship development
Clinical research compliance
Cultural competency
Financial operations management
Bachelor's degree
Managing clinical research teams
Contingency planning
Data interpretation
Contracts
Leading team collaboration initiatives
Compliance support tasks
Project budget management
Computer skills
Contract risk assessment
Project resource management
Project contract management
Cross-functional team management
Medical terminology
Project planning phase

Full Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join us as Start-up Team Manager - To manage complex site operations, ensure compliance with regulatory standards, support site recruitment and training efforts, and facilitate smooth collaboration between trial sites and internal teams to drive the success of clinical studies.

What You’ll Do:

Collaborate with multiple team members in a matrix environment for the effective delivery of site activation within the assigned projects.
May oversee site activation for assigned projects according to timelines and quality standard.
Assist with coordination of the flow of information between PPD teams, clients, or functional departments involved in site activation.
Develop recommended plans/guidelines for project implementation using PPD tools
Monitor and analyze project status to ensure successful progress and completion of all assigned projects and provide metrics to upper management.
Perform risk identification and provide contingency planning.
Collaborate with PPD teams to manage all financial and contractual aspects of studies related to site activation.
Work within the team to establish appropriate controls to ensure that project resources and expenses are aligned with budgets with accountability to Global

Project Management.

Administer the technical and operational aspects of the site activation portion of assigned projects, including coordination of feasibility, site contracts, and

country teams in a matrix environment and manages the assigned scope of work against timelines, costs, and quality.

Participating in a functional area leads to identifying and evaluating fundamental issues pertaining to successful site activation, interpreting data on complex issues,

make good business decisions and ensure solutions are implemented.

Develop customer relationships in alignment with assigned projects.

Education and Experience:

Bachelor's degree or equivalent and relevant formal academic / vocational qualification
Previous experience to provide the knowledge, skills, and abilities to perform the job (comparable to 5+ years’).
In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills and Abilities:

Able to work well and efficiently with cross-functional teams
Consistently demonstrates knowledge of the key principles of cross functional project management
Demonstrated organizational and multitasking skills
Demonstrated attention to detail
Ability to identify and remedy risks related to contractual deliverables and provides appropriate solutions
Demonstrates sound understanding of cross-cultural awareness and can adapt appropriately
Comprehensive understanding and appreciation of clinical research/ development, including medical and therapeutic areas, phases and medical terminology
Demonstrates ability to lead, liaise and coordinate cross-functional project teams
Comprehensive knowledge/understanding of clinical development guidelines and Directives

Working Conditions and Environment:

Work is performed in an office/ laboratory and/or a clinical environment.
Exposure to biological fluids with potential exposure to infectious organisms.
Exposure to electrical office equipment.
Personal protective equipment is required such as protective eyewear, garments and gloves.
Occasional travel, up to 20% of the time, includes travel to site locations both domestic and international. May include travel time outside of normal business hours and/or on weekends.

Physical Requirements:

Ability to work in an upright and /or stationary position for 6-8 hours per day.
Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.
Frequent mobility required.
Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.
Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
Ability to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences.
Frequently interacts with others to obtain or relate information to diverse groups.
Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to perform under stress. Ability to multi-task.
Regular and consistent attendance.

Why Join Us?
When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience – and where your contributions truly make a difference.

Apply today to help us deliver tomorrow’s breakthrough.

Apply Now

Refine Your Search

clinical study manager jobs in durham nc

Start-up Team Manager (STM) - FSP

Manager, Clinical Operations

Senior Clinical Trial Manager - Metabolic

Clinical Project Manager- IVD

RWE Clinical Project Manager (FSP)

Manager, Site Contracts with Clinical Trials experience Hybrid or Remote in USA-NC

Clinical Program Manager

Clinical Study Design Manager

(Senior) Clinical Study Manager, Clinical Development

Clinical Project Manager

Senior Clinical Trial Manager - Oncology

Manager, Site Contracts with Clinical Trials experience Hybrid or Remote in USA-NC

Clinical Lead- CVRM/MASH

Clinical Project Manager Director (MASH)

Senior Clinical Project Manager, Immuno-Oncology, IQVIA Biotech

Associate Clinical Lead Director

Associate Manager / Manager, Project Services - Laboratories (Remote - East Coast)

Senior Global Clinical Study Manager

Global Study Associate Director

Site Activation Manager

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