Top 29 Clinical research associate Jobs in Smithfield Nc

Sr. Clinical Team Manager - FSP
Thermo Fisher Scientific —North Carolina
- Full-time
- Remote
- Microsoft Excel
- Microsoft Outlook
- English
5d
Principal Clinical Trial Coordinator - FSP
Thermo Fisher Scientific —North Carolina
- Full-time
- Remote
- Office
- Bachelor's degree
- Team management
2d
Country Approval Specialist - FSP
Thermo Fisher Scientific —North Carolina
- Full-time
- Remote
- English
- Mid-level
- Office
Manager, Clinical Operations - FSP
Thermo Fisher Scientific —North Carolina
- $115,000 - $195,500 a year
- Full-time
- Remote
- English
- Business development
- Travel
- Commuter assistance
- Paid parental leave
Clinical Research Associate II/III - US
Optimapharm d.o.o. —Raleigh, NC
- $75,000 - $100,000 a year
- Full-time
- Remote
- Nursing
- Computer literacy
- Mid-level
- Dental insurance
- Paid time off
Clinical Research Coordinator - Raleigh, NC
IQVIA —Raleigh, NC
- $35 - $42 an hour
- Part-time
- Vital signs
- Office
- Bachelor's degree
10d
Senior Clinical Research Associate - US
Optimapharm d.o.o. —Raleigh, NC
- $100,000 - $130,000 a year
- Full-time
- Remote
- Nursing
- 5 years
- Computer literacy
- Dental insurance
- Paid time off
Clinical Research Associate/Pharmacy Tech.
Southeastern Medical Oncology Center —Goldsboro, NC
- Full-time
- Ability to walk for extended periods
- Mid-level
- High school diploma or GED
- Paid holidays
- Paid time off
Quick Apply
10d
Sr Clinical Research Associate
Veranex, Inc. —Raleigh, NC
- $98,400 - $140,690 a year
- Full-time
- Remote
- Microsoft Excel
- Microsoft Outlook
- 5 years
Quick Apply
Clinical Research Coordinator I
Care Access —Raleigh, NC
- $55,000 - $85,000 a year
- Microsoft Word
- Patient monitoring
- Writing skills
- Health savings account
- Paid holidays
5d
Senior Clinical Research Associate
Ergomed —Raleigh, NC
- Full-time
- Remote
- English
- Travel
- Senior level
Quick Apply
Clinical Research Coordinator I
Ora —Raleigh, NC
- Weekends as needed
- Vital signs
- Clinic experience
- Clinic
- Dental insurance
Quick Apply
Certified Medical Assistant, POD
Southeastern Medical Oncology Center —Goldsboro, NC
- 8 hour shift
- Mid-level
- In-person
- Certified Medical Assistant
- Disability insurance
- Health insurance
Quick Apply
Global Clinical Lead / Global Lead
Parexel —Raleigh, NC
- Nursing
- 5 years
- Continuous improvement
Clinical Trials Manager
Kite Pharma —Raleigh, NC
- $133,195 - $189,640 a year
- Full-time
- 6 years
- Surgery
- RN License
- Health insurance
- Dental insurance
Senior Clinical Project Manager
Azurity Pharmaceuticals - US —Raleigh, NC
- Full-time
- Hybrid work
- 5 years
- Office
- Ability to climb stairs
- Fuel card
- Health insurance
16h
Registered Nurse
Hawthorne Health, Inc. —Raleigh, NC
- Vital signs
- RN License
- English
Quick Apply
Region Manager
Care Access —Raleigh, NC
- $95,000 - $115,000 a year
- Up to 50% travel
- Inventory management
- Pass drug screening
- Health savings account
- Paid holidays
11d
Assistant/Associate/Full Clinical or Tenure Track Professor of Radiation Oncology
North Carolina State University —Raleigh, NC
- Monday to Friday
- US work authorization
- Military encouraged
- Senior level
- Paid holidays
- Disability insurance

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Principal Clinical Trial Coordinator - FSP
Thermo Fisher Scientific —North Carolina
Support study close-out activities including final TMF Review and TMF certification form (DEV-FORM-1939) completion.
2d

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Clinical Research Assistant 2-Hematology
The Ohio State University Wexner Medical Center —Columbus, OH
Bachelor’s Degree in Biological Sciences, Health Sciences or medical field, or equivalent combination of education experience required.
4d
Clinical Research Coordinator
OhioHealth —Columbus, OH
This position performs basic day to day activities related to clinical research studies including recruit and screen participants, obtains informed consent,…

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Sr. Clinical Team Manager - FSP

Thermo Fisher Scientific -
North Carolina

Apply Now

Job Details

Full-time
5 days ago

Qualifications

Customer communication
Delegation

Full Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Senior Clinical Trial/Team Manager (CTM) - Make an Impact at the Forefront of Innovation

The Senior Clinical Trial/Team Manager (CTM) is accountable for achieving the final clinical deliverable (usually clean data from evaluable patients as specified in the study protocol) within the time period specified in the contract with the customer. Interprets data on complex issues and makes good business decisions with support from line management. The role involves working to ensure that all clinical deliverables meet the customer's time/quality/cost expectations, and maintaining profitability by ensuring clinical activity is conducted within contract scope, through efficient management of the clinical team. Typically, the Senior Clinical Trial/Team Manager (CTM) works independently on projects of moderate to high complexity and may assume regional lead or Clinical Study Manager responsibilities.

Start-up experience required. As CTM will be responsible for submissions.

What You'll Do:

Manage all clinical operational and quality aspects of allocated studies, of moderate to high complexity, in compliance with ICH GCP. In accordance to project specific requirements, may assume Lead CTM responsibilities on regional level, Clinical Study Manager (CSM) responsibilities or take on additional responsibilities, e.g. process improvements, manage complex programs, have wider management or project coordination responsibilities.
Develop clinical tools (e.g. Monitoring Plan, Monitoring Guidelines) in conjunction with the Data Quality Plan. Contribute to the development of the Master Action Plan (MAP) for providing clinical related documents. Ensure timely set up, organization, content and quality of the relevant sections of the Trial Master File (local and central). May participate in the design and development of CRFs, CRF guidelines, patient informed consent templates and other protocol specific documents as required. Collaborate with the project manager to prepare, organize, and present at client meetings, including bid defense and hand-off meetings.
Collaborate with the clinical team and other departments as needed to meet deliverables of the project. Regularly communicate with the team and leads team meetings to ensure that timelines, resources, interactions, and quality are maintained. Responsible for the implementation and training of standardized clinical monitoring processes within the study and according to corporate standard policies. Responsible for the timely archiving of documents and study materials for the department.
Ensure achievement of the final clinical deliverable within the contractual time period specified by preparing and monitoring clinical activity timelines and metrics, providing status updates to the project manager, regularly reviewing projects using tracking and management tools, implementing recovery actions, reviewing monitoring visit reports, and managing CRF collection and query resolution. Continuously monitor clinical trials to assess performance and ensure contractual obligations are met. May routinely conduct Accompanied Field Visits (AFVs) and be accountable for project financials.
Communicate with study sites regarding issues such as protocol, patient participation, case report form completion and other study-related issues.
May coordinate all start-up activities, and ensure that essential document quality meets the expectation of Regulatory Compliance Review. Ensure timely regulatory submissions (if appropriate) are addressed. Reviews and follows up on all questions raised by ethics committees. Responsibility may vary based on project timelines.
Provide input into preparation of forecast estimates for clinical activities.
Responsible for clinical resource management, assignment, delegation of clinical responsibilities and identification of additional resource requirements.
In North America, where assigned to GPHS (Government & Public Health Studies) projects, may have limited line management responsibilities.

Education & Experience Requirements:

Bachelor's degree or equivalent and relevant formal academic / vocational qualification
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 8+ 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, Abilities:

Strong leadership skills, effective at mentoring and training, and capable of motivating and integrating teams.
Strong planning and organizational skills to enable effective prioritization of workload and workload of team members
Strong interpersonal and problem solving skills to enable working in a multicultural matrix organization
Solid understanding of change management principles
Comprehensive understanding of the practices, processes, and requirements of clinical monitoring
Strong judgment, decision making, escalation, and risk management skills
Effective oral and written communication skills, including English language proficiency
Capable of evaluating own and team members workload against project budget and adjust resources accordingly
Strong financial acumen and knowledge of budgeting, forecasting and fiscal management
Strong attention to detail
In-depth understanding of relevant regulations e.g. ICH/GCP, FDA guidelines, etc.
Strong computer skills to effectively use automated systems and computerized applications such as Outlook, Excel, Word, etc.
Capable of independently managing clinical only studies.

Working Conditions and Environment:

Work is performed in an office environment with exposure to electrical office equipment.
Frequently drives to site locations and frequently travels both domestic and international.

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 breakthroughs.

Apply Now

Refine Your Search

clinical research associate jobs in smithfield nc

Sr. Clinical Team Manager - FSP

Principal Clinical Trial Coordinator - FSP

Country Approval Specialist - FSP

Manager, Clinical Operations - FSP

Clinical Research Associate II/III - US

Clinical Research Coordinator - Raleigh, NC

Senior Clinical Research Associate - US

Clinical Research Associate/Pharmacy Tech.

Sr Clinical Research Associate

Clinical Research Coordinator I

Senior Clinical Research Associate

Clinical Research Coordinator I

Certified Medical Assistant, POD

Global Clinical Lead / Global Lead

Clinical Trials Manager

Senior Clinical Project Manager

Registered Nurse

Region Manager

Assistant/Associate/Full Clinical or Tenure Track Professor of Radiation Oncology

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