Durham, NC · On-site
$47K - $123K/yr
... SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project ... Perform start up and site activation activities according to applicable regulations, SOPs and work ...
Durham, NC · On-site
$47K - $123K/yr
... SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project ... Perform start up and site activation activities according to applicable regulations, SOPs and work ...
Raleigh, NC · On-site
$23.50 - $31.25/hr
Ensure protocol compliance and participant safety throughout the study. Assist with study start-up, close-out activities, and regulatory submissions. Required Qualifications Bachelor's or Master ...
Quick apply
Raleigh, NC · On-site
$23.50 - $31.25/hr
Ensure protocol compliance and participant safety throughout the study. Assist with study start-up, close-out activities, and regulatory submissions. Required Qualifications Bachelor's or Master ...
... study start-up activities such as working with sites to collect appropriate regulatory documents ... Associate * 4-year universitydegree OR Nursing Degree * Experience in Oncology is required
... study start-up activities such as working with sites to collect appropriate regulatory documents ... Associate * 4-year universitydegree OR Nursing Degree * Experience in Oncology is required
Durham, NC · On-site
... study start-up activities such as working with sites to collect appropriate regulatory documents ... Associate * 4-year university degree OR Nursing Degree * Experience in Oncology is required
Durham, NC · On-site
... study start-up activities such as working with sites to collect appropriate regulatory documents ... Associate * 4-year university degree OR Nursing Degree * Experience in Oncology is required
Ensure that proper guidelines for communication are set at study start-up and maintained throughout a study by creating and updating the study specific Communication and Escalation Plan. Ensure ...
Ensure that proper guidelines for communication are set at study start-up and maintained throughout a study by creating and updating the study specific Communication and Escalation Plan. Ensure ...
Durham, NC · On-site
$66K - $83K/yr
Graduation from an accredited BSN program , or Associate Degree in Nursing, or Nursing Diploma ... Coordinate and manage complex oncology clinical trials , including study start-up, participant ...
Durham, NC · On-site
$66K - $83K/yr
Graduation from an accredited BSN program , or Associate Degree in Nursing, or Nursing Diploma ... Coordinate and manage complex oncology clinical trials , including study start-up, participant ...
Durham, NC · On-site
$66K - $83K/yr
Graduation from an accredited BSN program , or Associate Degree in Nursing, or Nursing Diploma ... Coordinate and manage complex oncology clinical trials , including study start-up, participant ...
Durham, NC · On-site
$66K - $83K/yr
Graduation from an accredited BSN program , or Associate Degree in Nursing, or Nursing Diploma ... Coordinate and manage complex oncology clinical trials , including study start-up, participant ...
Raleigh, NC · On-site +1
With operations in 40+ countries and 2x the patient reach of the average mid-sized CRO, we enable accelerated regulatory pathways, faster study start-up, and access to diverse patient populations ...
Raleigh, NC · On-site +1
With operations in 40+ countries and 2x the patient reach of the average mid-sized CRO, we enable accelerated regulatory pathways, faster study start-up, and access to diverse patient populations ...
Durham, NC · On-site
$23.50 - $31.25/hr
... as study start up and close out, IRB tasks, etc.). You will have an essential role in the ... Completion of an Associate's degree Experience * Work requires a minimum of two years of relevant ...
Durham, NC · On-site
$23.50 - $31.25/hr
... as study start up and close out, IRB tasks, etc.). You will have an essential role in the ... Completion of an Associate's degree Experience * Work requires a minimum of two years of relevant ...
Durham, NC · On-site
$23.50 - $31.25/hr
... as study start up and close out, IRB tasks, etc.). You will have an essential role in the ... Completion of an Associate's degree Experience * Work requires a minimum of two years of relevant ...
Durham, NC · On-site
$23.50 - $31.25/hr
... as study start up and close out, IRB tasks, etc.). You will have an essential role in the ... Completion of an Associate's degree Experience * Work requires a minimum of two years of relevant ...
Durham, NC · On-site +1
With operations in 40+ countries and 2x the patient reach of the average mid-sized CRO, we enable accelerated regulatory pathways, faster study start-up, and access to diverse patient populations ...
Durham, NC · On-site +1
With operations in 40+ countries and 2x the patient reach of the average mid-sized CRO, we enable accelerated regulatory pathways, faster study start-up, and access to diverse patient populations ...
Durham, NC · On-site +1
Serve as the primary point of accountability for site activation and start-up activities on assigned studies. * Oversee cross-functional site activation activities to ensure milestones are achieved ...
Durham, NC · On-site +1
Serve as the primary point of accountability for site activation and start-up activities on assigned studies. * Oversee cross-functional site activation activities to ensure milestones are achieved ...
Durham, NC · On-site
$23.50 - $31.25/hr
As a valued member of our research team, you will independently coordinate and manage clinical research studies from study start-up through closeout while ensuring compliance with institutional ...
Durham, NC · On-site
$23.50 - $31.25/hr
As a valued member of our research team, you will independently coordinate and manage clinical research studies from study start-up through closeout while ensuring compliance with institutional ...
Ensure that proper guidelines for communication are set at study start-up and maintained throughout a study by creating and updating the study specific Communication and Escalation Plan. Ensure ...
Quick apply
Ensure that proper guidelines for communication are set at study start-up and maintained throughout a study by creating and updating the study specific Communication and Escalation Plan. Ensure ...
Provide oversight and direction to study team members for study deliverables, study start up and oversight: Accountable for the identification, bid process, and final selection of vendor(s), oversee ...
Provide oversight and direction to study team members for study deliverables, study start up and oversight: Accountable for the identification, bid process, and final selection of vendor(s), oversee ...
Durham, NC · On-site
$23.50 - $31.25/hr
As a valued member of our research team, you will independently coordinate and manage clinical research studies from study start-up through closeout while ensuring compliance with institutional ...
Durham, NC · On-site
$23.50 - $31.25/hr
As a valued member of our research team, you will independently coordinate and manage clinical research studies from study start-up through closeout while ensuring compliance with institutional ...
Durham, NC · On-site
Provide oversight and direction to study team members for study deliverables, study start up and oversight: Accountable for the identification, bid process, and final selection of vendor(s), oversee ...
Durham, NC · On-site
Provide oversight and direction to study team members for study deliverables, study start up and oversight: Accountable for the identification, bid process, and final selection of vendor(s), oversee ...
Durham, NC · On-site
Provide oversight and direction to study team members for study deliverables, study start up and oversight: Accountable for the identification, bid process, and final selection of vendor(s), oversee ...
Durham, NC · On-site
Provide oversight and direction to study team members for study deliverables, study start up and oversight: Accountable for the identification, bid process, and final selection of vendor(s), oversee ...
Durham, NC · On-site
Provide oversight and direction to study team members for study deliverables, study start up and oversight: Accountable for the identification, bid process, and final selection of vendor(s), oversee ...
Durham, NC · On-site
Provide oversight and direction to study team members for study deliverables, study start up and oversight: Accountable for the identification, bid process, and final selection of vendor(s), oversee ...
Durham, NC · On-site
Provide oversight and direction to study team members for study deliverables, study start up and oversight: Accountable for the identification, bid process, and final selection of vendor(s), oversee ...
Durham, NC · On-site
Provide oversight and direction to study team members for study deliverables, study start up and oversight: Accountable for the identification, bid process, and final selection of vendor(s), oversee ...
$12.38 - $16.14
3% of jobs
$16.14 - $19.90
18% of jobs
$20.65 is the 25th percentile. Wages below this are outliers.
$19.90 - $23.66
20% of jobs
The median wage is $25.95 / hr.
$23.66 - $27.42
15% of jobs
$27.42 - $31.18
11% of jobs
$31.18 - $34.94
4% of jobs
$38.14 is the 75th percentile. Wages above this are outliers.
$34.94 - $38.70
5% of jobs
$38.70 - $42.46
8% of jobs
$42.46 - $46.22
6% of jobs
$46.22 - $49.98
6% of jobs
$49.98 - $53.74
3% of jobs
$12
$30
$53
| Aspect | Study Start Up Associate | Clinical Trial Coordinator |
|---|---|---|
| Required Credentials | Bachelor's degree, knowledge of regulatory requirements | Bachelor's degree, familiarity with clinical procedures |
| Work Environment | Regulatory and site initiation activities | Participant management and site coordination |
| Employer & Industry Usage | Pharmaceuticals, biotech, CROs | Hospitals, research centers, CROs |
The Study Start Up Associate primarily focuses on regulatory submissions, site qualification, and initiation processes, ensuring trial readiness. In contrast, the Clinical Trial Coordinator manages participant recruitment, scheduling, and data collection. Both roles are essential in clinical research but differ in their core responsibilities and focus areas.
For Study Start Up Associate jobs in Raleigh, NC, the most frequently searched job titles are:
The top searched job categories for Study Start Up Associate jobs in Raleigh, NC are:
Cities near Raleigh, NC with the most Study Start Up Associate job openings:
Durham, NC • On-site
$47K - $123K/yr
Full-time
Posted 12 days ago
Perform site activation and start-up activities in accordance with regulations, SOPs, and project requirements.
Serve as Single Point of Contact (SPOC) for investigative sites, project teams, and other departments, ensuring communication and document distribution.
Review, track, and ensure the completion and accuracy of regulatory documents, site performance metrics, and project timelines.
8.1
Based on 53 frontline employees who took The Breakroom Quiz
Job Overview
Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities.
Essential Functions
Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary. Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of designated deliverables and project timelines.
Perform start up and site activation activities according to applicable regulations, SOPs and work instructions. Distribute completed documents to sites and internal project team members.
Prepare site regulatory documents, reviewing for completeness and accuracy.
Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information.
Review and provide feedback to management on site performance metrics.
Review, establish and agree on project planning and project timelines. Ensure monitoring measures are in place and implement contingency plan as needed.
Inform team members of completion of regulatory and contractual documents for individual sites.
Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents, in line with project timelines.
Provide local expertise to SAMs and project team during initial and on-going project timeline planning.
Perform quality control of documents provided by sites.
May have direct contact with sponsors on specific initiatives.
Qualifications
1 year clinical research experience. Equivalent combination of education, training and experience.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role, when annualized, is $47,700.00 - $123,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
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At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.
Health care and social assistance
10,000+ Employees
Durham, NC, US
