Collegeville, PA · On-site
$54K - $71K/yr
Alliance Partner/ CRO ,Regulatory Affairs, Legal, Pharm Sci, Contracts and Outsourcing) to implement one or more clinical protocols, with focus on study start-up and recruitment phases. Will be an ...
Collegeville, PA · On-site
$54K - $71K/yr
Alliance Partner/ CRO ,Regulatory Affairs, Legal, Pharm Sci, Contracts and Outsourcing) to implement one or more clinical protocols, with focus on study start-up and recruitment phases. Will be an ...
Study Start-Up and Site Activation * Lead or significantly contribute to study start-up activities including site feasibility, vendor coordination, regulatory package readiness, and site activation ...
Study Start-Up and Site Activation * Lead or significantly contribute to study start-up activities including site feasibility, vendor coordination, regulatory package readiness, and site activation ...
Blue Bell, PA · Remote
Developing and implementing comprehensive strategies for study start-up, site activation, and regulatory delivery that align with organizational goals, client expectations, and evolving industry ...
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Blue Bell, PA · Remote
Developing and implementing comprehensive strategies for study start-up, site activation, and regulatory delivery that align with organizational goals, client expectations, and evolving industry ...
Blue Bell, PA · Remote
Developing and implementing comprehensive strategies for study start-up, site activation, and regulatory delivery that align with organizational goals, client expectations, and evolving industry ...
Blue Bell, PA · Remote
Developing and implementing comprehensive strategies for study start-up, site activation, and regulatory delivery that align with organizational goals, client expectations, and evolving industry ...
Blue Bell, PA · On-site
Developing and implementing comprehensive strategies for study start-up, site activation, and regulatory delivery that align with organizational goals, client expectations, and evolving industry ...
Blue Bell, PA · On-site
Developing and implementing comprehensive strategies for study start-up, site activation, and regulatory delivery that align with organizational goals, client expectations, and evolving industry ...
Reading, PA · Remote
Developing and implementing comprehensive strategies for study start-up, site activation, and regulatory delivery that align with organizational goals, client expectations, and evolving industry ...
Reading, PA · Remote
Developing and implementing comprehensive strategies for study start-up, site activation, and regulatory delivery that align with organizational goals, client expectations, and evolving industry ...
Malvern, PA · On-site
Study Start-Up and Site Activation * Lead or significantly contribute to study start-up activities including site feasibility, vendor coordination, regulatory package readiness, and site activation ...
Malvern, PA · On-site
Study Start-Up and Site Activation * Lead or significantly contribute to study start-up activities including site feasibility, vendor coordination, regulatory package readiness, and site activation ...
Train and mentor Clinical Research Associates (CRAs) to optimize their performance. * Timely Study Start-Up & Enrollment: Drive enrollment and lead study start-up activities, adhering to timelines.
Train and mentor Clinical Research Associates (CRAs) to optimize their performance. * Timely Study Start-Up & Enrollment: Drive enrollment and lead study start-up activities, adhering to timelines.
Blue Bell, PA · On-site +1
Train and mentor Clinical Research Associates (CRAs) to optimize their performance. * Timely Study Start-Up & Enrollment: Drive enrollment and lead study start-up activities, adhering to timelines.
Blue Bell, PA · On-site +1
Train and mentor Clinical Research Associates (CRAs) to optimize their performance. * Timely Study Start-Up & Enrollment: Drive enrollment and lead study start-up activities, adhering to timelines.
Support study acquisition and activation functions in collaboration with global shared services team to meet START goals for speedy study start up and network-wide study acquisition functions ...
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Support study acquisition and activation functions in collaboration with global shared services team to meet START goals for speedy study start up and network-wide study acquisition functions ...
Support study acquisition and activation functions in collaboration with global shared services team to meet START goals for speedy study start up and network-wide study acquisition functions ...
Support study acquisition and activation functions in collaboration with global shared services team to meet START goals for speedy study start up and network-wide study acquisition functions ...
Support study acquisition and activation functions in collaboration with global shared services team to meet START goals for speedy study start up and network-wide study acquisition functions ...
Support study acquisition and activation functions in collaboration with global shared services team to meet START goals for speedy study start up and network-wide study acquisition functions ...
Blue Bell, PA · On-site +1
May manage the study start up process in countries assigned (where SUPM not assigned) and/or ... Effective verbal and written communication skills in relating to colleagues and associates both ...
Blue Bell, PA · On-site +1
May manage the study start up process in countries assigned (where SUPM not assigned) and/or ... Effective verbal and written communication skills in relating to colleagues and associates both ...
May manage the study start up process in countries assigned (where SUPM not assigned) and/or ... Effective verbal and written communication skills in relating to colleagues and associates both ...
May manage the study start up process in countries assigned (where SUPM not assigned) and/or ... Effective verbal and written communication skills in relating to colleagues and associates both ...
May manage the study start up process in countries assigned (where SUPM not assigned) and/or ... Effective verbal and written communication skills in relating to colleagues and associates both ...
Quick apply
May manage the study start up process in countries assigned (where SUPM not assigned) and/or ... Effective verbal and written communication skills in relating to colleagues and associates both ...
Monroeville, PA · On-site
$24 - $32/hr
Coordinate and manage day-to-day clinical trial activities from study start-up through close-out * Schedule and conduct study visits in accordance with protocol requirements * Ensure proper informed ...
Monroeville, PA · On-site
$24 - $32/hr
Coordinate and manage day-to-day clinical trial activities from study start-up through close-out * Schedule and conduct study visits in accordance with protocol requirements * Ensure proper informed ...
The Study Specialist will augment activities performed by existing study team members whether from ... Removing site obstacles to site start-up, maintenance and close-out while maintaining awareness of ...
The Study Specialist will augment activities performed by existing study team members whether from ... Removing site obstacles to site start-up, maintenance and close-out while maintaining awareness of ...
Monroeville, PA · On-site
$53K - $58K/yr
Coordinate and manage day-to-day clinical trial activities from study start-up through close-out * Schedule and conduct study visits in accordance with protocol requirements * Ensure proper informed ...
Monroeville, PA · On-site
$53K - $58K/yr
Coordinate and manage day-to-day clinical trial activities from study start-up through close-out * Schedule and conduct study visits in accordance with protocol requirements * Ensure proper informed ...
Monroeville, PA · On-site
$24 - $32/hr
Coordinate and manage day-to-day clinical trial activities from study start-up through close-out * Schedule and conduct study visits in accordance with protocol requirements * Ensure proper informed ...
Quick apply
Monroeville, PA · On-site
$24 - $32/hr
Coordinate and manage day-to-day clinical trial activities from study start-up through close-out * Schedule and conduct study visits in accordance with protocol requirements * Ensure proper informed ...
Fountain Hill, PA · On-site
$57.50 - $69.25/hr
Attend Site Initiation Visits (SIVs) to support investigational drug product planning, study start-up, site readiness, and activation. * Attend and contribute to Study Feasibility and Billing ...
Fountain Hill, PA · On-site
$57.50 - $69.25/hr
Attend Site Initiation Visits (SIVs) to support investigational drug product planning, study start-up, site readiness, and activation. * Attend and contribute to Study Feasibility and Billing ...
$12.77 - $16.65
3% of jobs
$16.65 - $20.53
18% of jobs
$21.29 is the 25th percentile. Wages below this are outliers.
$20.53 - $24.40
20% of jobs
The median wage is $26.76 / hr.
$24.40 - $28.28
15% of jobs
$28.28 - $32.16
11% of jobs
$32.16 - $36.03
4% of jobs
$39.33 is the 75th percentile. Wages above this are outliers.
$36.03 - $39.91
5% of jobs
$39.91 - $43.79
8% of jobs
$43.79 - $47.67
6% of jobs
$47.67 - $51.54
6% of jobs
$51.54 - $55.42
3% of jobs
$12
$31
$55
| 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 Pennsylvania, the most frequently searched job titles are:
The top searched job categories for Study Start Up Associate jobs in Pennsylvania are:
Cities in Pennsylvania with the most Study Start Up Associate job openings:
Collegeville, PA • On-site
$54K - $71K/yr
Contractor
Re-posted 26 days ago
A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.
This is Direct Hire Position with one of our Clients (7 to 10 Years of Total Experience)
Responsible for working collaboratively with the Lead Study Clinician, Clinical Operations Study Team Lead (COSTL), and other members of the Study Team (e.g. Alliance Partner/ CRO ,Regulatory Affairs, Legal, Pharm Sci, Contracts and Outsourcing) to implement one or more clinical protocols, with focus on study start-up and recruitment phases.
Will be an integral study team member and key member of study feasibility team to identify, evaluate and select clinical sites and investigators.
May be responsible for developing a site back-up plan that can be executed to support agreed timelines for study completion.
Primary focus will be site communication to ensure site is knowledgeable on protocol requirements, recruitment and retention planning, solution and relationship building during the study start-up phase to optimize completion time for the clinical trial start-up phase and ensure site is ready to screen subjects immediately after initiation occurs. Work closely with sites to proactively identify, manage and timely resolve study start-up up challenges, bottlenecks, site concerns.
Mid-level - Prefer ~5+ years 'experience in clinical trial execution .
Must have thorough understanding local and international regulations applicable to clinical trials.
The candidate experience should not solely be operational but rather have experience in alignment with our current Clinician position roles and responsibilities .
The candidate must have EXCELLENT communication skills and be thoroughly comfortable in speaking with prospective PIs and Study Coordinators.
Must be proficient in collaborative problem-solving skills (A prior CRA or someone with Study Coordinator experience would be a good fit for this position.)
BA/BS or Higher Degree preferred (M.S/PhD/PharmD/MD)
4-7 years of experience in Good Clinical Practices (GCP)
4-7 years of experience in Clinical Trials Safety Reporting
Contact-
Ricky Bansal
732-429-1925
Sourced by ZipRecruiter
Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.
Recruiting and staffing services
51 - 200 Employees
Edison, NJ, US
1996
