... clinical trials from startup to closeout Liaise with other functional areas to identify issues ... Communicate with Principle Investigator, Study Co-Coordinator, and/ CRO (if applicable) to ...
... clinical trials from startup to closeout Liaise with other functional areas to identify issues ... Communicate with Principle Investigator, Study Co-Coordinator, and/ CRO (if applicable) to ...
... clinical trials from startup to closeout Liaise with other functional areas to identify issues ... Communicate with Principle Investigator, Study Co-Coordinator, and/ CRO (if applicable) to ...
... clinical trials from startup to closeout Liaise with other functional areas to identify issues ... Communicate with Principle Investigator, Study Co-Coordinator, and/ CRO (if applicable) to ...
Clinical Study Manager
Cleveland, OH · On-site
$90K - $120K/yr
Manage end-to-end lifecycle of assigned IVD clinical research projects, including startup, site ... Build study budgets and timelines, establish milestones, and coordinate site selection and ...
Clinical Study Manager
Cleveland, OH · On-site
$90K - $120K/yr
Manage end-to-end lifecycle of assigned IVD clinical research projects, including startup, site ... Build study budgets and timelines, establish milestones, and coordinate site selection and ...
Clinical Study Manager
Cleveland, OH · On-site
$90K - $120K/yr
Manage end-to-end lifecycle of assigned IVD clinical research projects, including startup, site ... Build study budgets and timelines, establish milestones, and coordinate site selection and ...
Clinical Study Manager
Cleveland, OH · On-site
$90K - $120K/yr
Manage end-to-end lifecycle of assigned IVD clinical research projects, including startup, site ... Build study budgets and timelines, establish milestones, and coordinate site selection and ...
Regulatory Coordinator I - Study Activation
Saint Petersburg, FL · On-site
$23 - $30.50/hr
This position is grant-funded for a period of five years and is therefore considered temporary in ... startup process OR * * Associate's degree PLUS * 6 years of experience in clinical research ...
Regulatory Coordinator I - Study Activation
Saint Petersburg, FL · On-site
$23 - $30.50/hr
This position is grant-funded for a period of five years and is therefore considered temporary in ... startup process OR * * Associate's degree PLUS * 6 years of experience in clinical research ...
Director, Clinical Science
New York, NY · On-site
$200K - $240K/yr
You own protocol development, data review, clinical document authorship, and site-level scientific support from study startup through closeout. You will work closely with Clinical Operations ...
Director, Clinical Science
New York, NY · On-site
$200K - $240K/yr
You own protocol development, data review, clinical document authorship, and site-level scientific support from study startup through closeout. You will work closely with Clinical Operations ...
... clinical trials from startup to closeout Liaise with other functional areas to identify issues ... Communicate with Principle Investigator, Study Co-Coordinator, and/ CRO (if applicable) to ...
... clinical trials from startup to closeout Liaise with other functional areas to identify issues ... Communicate with Principle Investigator, Study Co-Coordinator, and/ CRO (if applicable) to ...
Clinical Study Coordinator/Manager
Milford, MA · On-site
$25 - $30/hr
- Clinical Study Manager/Coordinator About the Company: Propedix is a biopharma and consumer health ... paced startup environment. Key Responsibilities: Study Start-Up & Regulatory · Support and ...
Quick apply
Clinical Study Coordinator/Manager
Milford, MA · On-site
$25 - $30/hr
- Clinical Study Manager/Coordinator About the Company: Propedix is a biopharma and consumer health ... paced startup environment. Key Responsibilities: Study Start-Up & Regulatory · Support and ...
Regulatory Coordinator I - Study Activation
Saint Petersburg, FL · On-site
$23.25 - $31/hr
This position is grant-funded for a period of five years and is therefore considered temporary in ... startup process OR * Associate's degree PLUS * 6 years of experience in clinical research ...
Regulatory Coordinator I - Study Activation
Saint Petersburg, FL · On-site
$23.25 - $31/hr
This position is grant-funded for a period of five years and is therefore considered temporary in ... startup process OR * Associate's degree PLUS * 6 years of experience in clinical research ...
Temporary / Contract Pay: $46/hr - $48/hr on W2(Inclusive all) Position Summary Client is seeking ... study startup through study closeout. This role will be responsible for ensuring the quality ...
Quick apply
Temporary / Contract Pay: $46/hr - $48/hr on W2(Inclusive all) Position Summary Client is seeking ... study startup through study closeout. This role will be responsible for ensuring the quality ...
Clinical Study Coordinator/Manager
Milford, MA · On-site
$25 - $30/hr
- Clinical Study Manager/Coordinator About the Company: Propedix is a biopharma and consumer health ... paced startup environment. Key Responsibilities: Study Start-Up & Regulatory · Support and ...
Quick apply
Clinical Study Coordinator/Manager
Milford, MA · On-site
$25 - $30/hr
- Clinical Study Manager/Coordinator About the Company: Propedix is a biopharma and consumer health ... paced startup environment. Key Responsibilities: Study Start-Up & Regulatory · Support and ...
Lead study startup activities including CRO RFP coordination, proposal evaluation, and contract ... Minimum 8 years of clinical trial operations experience in the pharmaceutical or biotechnology ...
Quick apply
Lead study startup activities including CRO RFP coordination, proposal evaluation, and contract ... Minimum 8 years of clinical trial operations experience in the pharmaceutical or biotechnology ...
Clinical Scientist Location: Palo Alto, CA As a Clinical Scientist, you will support the Clinical ... Support study startup activities, including IRB submissions and coordination with internal teams
Clinical Scientist Location: Palo Alto, CA As a Clinical Scientist, you will support the Clinical ... Support study startup activities, including IRB submissions and coordination with internal teams
Clinical Scientist
Guilford, CT · On-site
Clinical Scientist Location: Guilford, CT (Onsite) As a Clinical Scientist, you will support the ... Support study startup activities, including IRB submissions and coordination with internal teams
Clinical Scientist
Guilford, CT · On-site
Clinical Scientist Location: Guilford, CT (Onsite) As a Clinical Scientist, you will support the ... Support study startup activities, including IRB submissions and coordination with internal teams
Role Overview The Sr. Manager, Clinical Trial Operations Planning & Analytics is responsible for ... This role will establish scalable approaches for feasibility, site identification, study startup ...
Role Overview The Sr. Manager, Clinical Trial Operations Planning & Analytics is responsible for ... This role will establish scalable approaches for feasibility, site identification, study startup ...
Regulatory Specialist II (Office of Clinical Trials)
Baltimore, MD · On-site
$41K - $72K/yr
... clinical trials ... Startup activities include coordination of internal partners (study teams, central research ...
Regulatory Specialist II (Office of Clinical Trials)
Baltimore, MD · On-site
$41K - $72K/yr
... clinical trials ... Startup activities include coordination of internal partners (study teams, central research ...
Clinical Scientist
Guilford, CT · On-site
Clinical Scientist Location:Guilford, CT (Onsite) As a Clinical Scientist, you will support the ... Support study startup activities, including IRB submissions and coordination with internal teams
Clinical Scientist
Guilford, CT · On-site
Clinical Scientist Location:Guilford, CT (Onsite) As a Clinical Scientist, you will support the ... Support study startup activities, including IRB submissions and coordination with internal teams
Clinical Scientist Location: Palo Alto, CA As a Clinical Scientist, you will support the Clinical ... Support study startup activities, including IRB submissions and coordination with internal teams
Quick apply
Clinical Scientist Location: Palo Alto, CA As a Clinical Scientist, you will support the Clinical ... Support study startup activities, including IRB submissions and coordination with internal teams
Associate Director, Clinical Data Management
Bothell, WA · On-site
$190K - $205K/yr
Ensure CRO adherence to project timelines, from study startup through study closeout. * Collaborate with clinical study teams and vendors to ensure project deliverables are met with clinical study ...
Associate Director, Clinical Data Management
Bothell, WA · On-site
$190K - $205K/yr
Ensure CRO adherence to project timelines, from study startup through study closeout. * Collaborate with clinical study teams and vendors to ensure project deliverables are met with clinical study ...
This role supports clinical trial study startup, database build, edit check programming, system configuration, user acceptance testing, issue resolution, and production support. The ideal candidate ...
This role supports clinical trial study startup, database build, edit check programming, system configuration, user acceptance testing, issue resolution, and production support. The ideal candidate ...
Temporary Clinical Study Startup information
See salary details
$11.54 - $16.74
4% of jobs
$16.74 - $21.94
15% of jobs
$24.54 is the 25th percentile. Wages below this are outliers.
$21.94 - $27.14
13% of jobs
$27.14 - $32.34
8% of jobs
The median wage is $35.23 / hr.
$32.34 - $37.54
19% of jobs
$37.54 - $42.74
13% of jobs
$44.83 is the 75th percentile. Wages above this are outliers.
$42.74 - $47.95
10% of jobs
$47.95 - $53.15
5% of jobs
$53.15 - $58.35
11% of jobs
$58.35 - $63.55
1% of jobs
$63.55 - $68.75
1% of jobs
$11
$37
$68
How much do temporary clinical study startup jobs pay per hour?
As of Jul 13, 2026, the average hourly pay for temporary clinical study startup in the United States is $37.67, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $48.08 per hour, depending on experience, location, and employer.
What cities are hiring for Temporary Clinical Study Startup jobs? Cities with the most Temporary Clinical Study Startup job openings:
What are the most commonly searched types of Clinical Study Startup jobs? The most popular types of Clinical Study Startup jobs are:
What states have the most Temporary Clinical Study Startup jobs? States with the most job openings for Temporary Clinical Study Startup jobs include:
Other
Re-posted 8 days ago
Job description
Company Description
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.
Job Description
Provide operational leadership for assigned trials executing them on time and within budget
Overall coordination and management of clinical trials from startup to closeout
Liaise with other functional areas to identify issues, evaluate and make sound business decisions and ensure implementation of timely solutions.
Identify and select high-quality clinical vendors in conjunction with the appropriate team members
Work with the contracting/budgeting team to ensure that vendor responsibilities and payment terms are clearly defined.
Manage and effectively provide oversight of assigned clinical vendors and functional service providers to ensure data integrity and adherence with regulatory requirements.
Assure that team is receiving high quality, on time deliverables from internal and external vendors.
Collaborate with other team members to coordinate the development and finalization of key study documents including protocols, case reports forms, informed consent documents, study management plans and final clinical study reports.
Work with finance manager on financial aspects of the project(s), including milestone payments, and monthly pass through invoices
Lead or facilitate teleconferences with internal or external group.
Oversee Clinical Trial Coordinator for assigned project to ensure successful management of project(s), including development of the project plan, maintenance of trackers, and generation of metrics reports
Assume co-monitoring responsibilities as needed.
Communicate with Principle Investigator, Study Co-Coordinator, and/ CRO (if applicable) to proactively recognize problem situations and work with other team members as required to resolve issues
Manage the publication process in conjunction with the publications team to assure that submission timelines are met.
Monitor and report clinical trial status using standard and adhoc review & reporting procedures and identify issues that affect functions. Ensure that each function is accountable for their deliverables.
In collaboration with Project Management and utilizing various tracking mechanisms, manage clinical trial project milestones and budget. Proactively identify issues and escalate to appropriate managers.
Qualifications
Minimum BS or BA in related field; focusing on biological science or nursing preferred or equivalent. Advanced Degree preferred
At least 10 years of experience in the management of clinical trials, significant knowledge of overall clinical drug development and general clinical research operations in Big Pharma.
Ability to manage multiple projects simultaneously with strong organizational and planning skills.
Well-developed analytical and problem solving skills. Communicates issues to Director with action plans for resolution.
Knowledgeable in all required regulatory and compliance standards and guidelines including ICH-GCP.
Additional Information
Feel free to forward my email to your friends/colleagues who might be available. We do offer a referral bonus!!
Thank you for your time and for consideration. I look forward to hearing from you
Thanks!!
Regards,
Jasmine Jogewar
Sr. Clinical Recruiter
Integrated Resources, Inc.
IT Life Sciences Allied Healthcare CRO
Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I
(Direct) 732-844-8720| (F) 732-549-5549
www.irionline.com , www.linkedin.com/in/Jasmine-Jogewar
About Integrated Resources
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.
Industry
Recruiting and staffing services
Company size
51 - 200 Employees
Headquarters location
Edison, NJ, US
Year founded
1996