Participant Recruitment & Study Startup Manager ClariMed is seeking a Participant Recruitment ... Experience in participant recruitment, human factors research, clinical research, market research ...
Participant Recruitment & Study Startup Manager ClariMed is seeking a Participant Recruitment ... Experience in participant recruitment, human factors research, clinical research, market research ...
PA · On-site
Participant Recruitment & Study Startup Manager About ClariMed, Inc. ClariMed is a human-centered ... clinical operations. Visit us at www.ClariMed.com. At ClariMed * We believe in excellence ...
PA · On-site
Participant Recruitment & Study Startup Manager About ClariMed, Inc. ClariMed is a human-centered ... clinical operations. Visit us at www.ClariMed.com. At ClariMed * We believe in excellence ...
... clinical operations. Visit us at www.ClariMed.com. At ClariMed * We believe in excellence ... The Participant Recruitment & Study Startup Manager will serve as a key operational leader ...
... clinical operations. Visit us at www.ClariMed.com. At ClariMed * We believe in excellence ... The Participant Recruitment & Study Startup Manager will serve as a key operational leader ...
The ideal candidate will possess strong project management, stakeholder coordination, communication ... in study startup, clinical trial operations, and/or clinical trial management. * Strong ...
Quick apply
The ideal candidate will possess strong project management, stakeholder coordination, communication ... in study startup, clinical trial operations, and/or clinical trial management. * Strong ...
Clinical Trial Study Startup Specialist
New Brunswick, NJ · On-site
$75K - $90K/yr
The ideal candidate will possess strong project management, stakeholder coordination, communication ... in study startup, clinical trial operations, and/or clinical trial management. * Strong ...
Clinical Trial Study Startup Specialist
New Brunswick, NJ · On-site
$75K - $90K/yr
The ideal candidate will possess strong project management, stakeholder coordination, communication ... in study startup, clinical trial operations, and/or clinical trial management. * Strong ...
Clinical Trial Study Startup Specialist
New Brunswick, NJ · On-site
$75K - $90K/yr
The ideal candidate will possess strong project management, stakeholder coordination, communication ... in study startup, clinical trial operations, and/or clinical trial management. * Strong ...
Clinical Trial Study Startup Specialist
New Brunswick, NJ · On-site
$75K - $90K/yr
The ideal candidate will possess strong project management, stakeholder coordination, communication ... in study startup, clinical trial operations, and/or clinical trial management. * Strong ...
Clinical Trial Study Startup Specialist
New Brunswick, NJ · On-site
$75K - $90K/yr
The ideal candidate will possess strong project management, stakeholder coordination, communication ... in study startup, clinical trial operations, and/or clinical trial management. * Strong ...
Quick apply
Clinical Trial Study Startup Specialist
New Brunswick, NJ · On-site
$75K - $90K/yr
The ideal candidate will possess strong project management, stakeholder coordination, communication ... in study startup, clinical trial operations, and/or clinical trial management. * Strong ...
Clinical Trial Study Startup Navigator
New Brunswick, NJ · On-site
$75K - $95K/yr
The ideal candidate will possess strong project management, stakeholder coordination, communication ... in study startup, clinical trial operations, and/or clinical trial management. * Strong ...
Clinical Trial Study Startup Navigator
New Brunswick, NJ · On-site
$75K - $95K/yr
The ideal candidate will possess strong project management, stakeholder coordination, communication ... in study startup, clinical trial operations, and/or clinical trial management. * Strong ...
Clinical Study Operations Manager
Boston, MA · On-site +1
$90K - $110K/yr
As a Clinical Study Operations Manager within the Clinical Study Operations team, you will be ... You will oversee study startup planning, site onboarding and training, and ongoing operational ...
Clinical Study Operations Manager
Boston, MA · On-site +1
$90K - $110K/yr
As a Clinical Study Operations Manager within the Clinical Study Operations team, you will be ... You will oversee study startup planning, site onboarding and training, and ongoing operational ...
Develop and execute study startup strategy and maintain accountability for site activation progress ... Experience managing clinical trial timelines, budgets, operational deliverables, and external ...
Quick apply
Develop and execute study startup strategy and maintain accountability for site activation progress ... Experience managing clinical trial timelines, budgets, operational deliverables, and external ...
Title: Senior Clinical Trials Manager - European Medical Device Studies Status: Exempt, Remote ... study startup strategy and maintain accountability for site activation progress across ...
Title: Senior Clinical Trials Manager - European Medical Device Studies Status: Exempt, Remote ... study startup strategy and maintain accountability for site activation progress across ...
Develop and execute study startup strategy and maintain accountability for site activation progress ... Experience managing clinical trial timelines, budgets, operational deliverables, and external ...
Develop and execute study startup strategy and maintain accountability for site activation progress ... Experience managing clinical trial timelines, budgets, operational deliverables, and external ...
Clinical Study Operations Manager
Boston, MA · On-site +1
$90K - $110K/yr
As a Clinical Study Operations Manager within the Clinical Study Operations team, you will be ... You will oversee study startup planning, site onboarding and training, and ongoing operational ...
Clinical Study Operations Manager
Boston, MA · On-site +1
$90K - $110K/yr
As a Clinical Study Operations Manager within the Clinical Study Operations team, you will be ... You will oversee study startup planning, site onboarding and training, and ongoing operational ...
Clinical Study Site Lead
Tempe, AZ · On-site
... startup activities and successful enrollment in sponsor supported Clinical Studies, with specific focus on the current BRIDGES trial. Positioned between traditional clinical study site management and ...
Quick apply
Clinical Study Site Lead
Tempe, AZ · On-site
... startup activities and successful enrollment in sponsor supported Clinical Studies, with specific focus on the current BRIDGES trial. Positioned between traditional clinical study site management and ...
The Senior Clinical Research Associate (CRA) will own site activation, clinical study startup, site management, enrollment performance, and protocol execution across VahatiCor's cardiovascular ...
The Senior Clinical Research Associate (CRA) will own site activation, clinical study startup, site management, enrollment performance, and protocol execution across VahatiCor's cardiovascular ...
The Senior Manager, Study Start-up partners closely with the Clinical Operations study team leading ... Oversee the analysis of clinical trial data and its application to conduct accurate study startup ...
The Senior Manager, Study Start-up partners closely with the Clinical Operations study team leading ... Oversee the analysis of clinical trial data and its application to conduct accurate study startup ...
The Senior Clinical Research Associate (CRA) will own site activation, clinical study startup, site management, enrollment performance, and protocol execution across VahatiCor's cardiovascular ...
The Senior Clinical Research Associate (CRA) will own site activation, clinical study startup, site management, enrollment performance, and protocol execution across VahatiCor's cardiovascular ...
The Senior Clinical Research Associate (CRA) will own site activation, clinical study startup, site management, enrollment performance, and protocol execution across VahatiCor's cardiovascular ...
Quick apply
The Senior Clinical Research Associate (CRA) will own site activation, clinical study startup, site management, enrollment performance, and protocol execution across VahatiCor's cardiovascular ...
TheSenior Clinical Research Associate (CRA)will own site activation,clinical study startup, site management, enrollment performance, and protocol execution across VahatiCor'scardiovascular medical ...
TheSenior Clinical Research Associate (CRA)will own site activation,clinical study startup, site management, enrollment performance, and protocol execution across VahatiCor'scardiovascular medical ...
Global Study Managers (GSMs) provide operational leadership across the full clinical study ... Accountable for the development of realistic detailed study startup and/or study management ...
Global Study Managers (GSMs) provide operational leadership across the full clinical study ... Accountable for the development of realistic detailed study startup and/or study management ...
Clinical Study Startup Manager information
See salary details
$28.85 - $34.97
4% of jobs
$34.97 - $41.08
6% of jobs
$41.08 - $47.20
7% of jobs
$51.79 is the 25th percentile. Wages below this are outliers.
$47.20 - $53.32
9% of jobs
$53.32 - $59.44
15% of jobs
The median wage is $62.14 / hr.
$59.44 - $65.56
18% of jobs
$69.92 is the 75th percentile. Wages above this are outliers.
$65.56 - $71.68
21% of jobs
$71.68 - $77.80
7% of jobs
$77.80 - $83.92
6% of jobs
$83.92 - $90.03
3% of jobs
$90.03 - $96.15
2% of jobs
$28
$62
$96
How much do clinical study startup manager jobs pay per hour?
What does a clinical study startup manager do?
What are the key skills and qualifications needed to thrive as a clinical study startup manager?
What are some common challenges faced by clinical study startup managers during the site activation process?
What is the difference between Clinical Study Startup Manager vs Clinical Research Coordinator?
| Aspect | Clinical Study Startup Manager | Clinical Research Coordinator |
|---|---|---|
| Responsibilities | Oversees study initiation, site selection, regulatory submissions, and startup activities | Manages participant recruitment, data collection, and day-to-day study operations at sites |
| Required Credentials | Bachelor's degree, clinical research experience, knowledge of regulations | Bachelor's degree, clinical research experience, good clinical practice (GCP) training |
| Work Environment | Corporate or sponsor offices, clinical trial sites | Clinical trial sites, hospitals, research centers |
The Clinical Study Startup Manager focuses on preparing and initiating clinical trials, ensuring regulatory compliance and site readiness. In contrast, the Clinical Research Coordinator handles the daily operations at trial sites, managing participant interactions and data collection. Both roles require similar credentials and work in related environments, but their core responsibilities differ significantly.
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Cities with the most Clinical Study Startup Manager job openings:
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States with the most job openings for Clinical Study Startup Manager jobs include:
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For Clinical Study Startup Manager jobs, the most frequently searched job titles are:

Participant Recruitment & Study Startup Manager
Chadds Ford, PA • On-site
Other
Re-posted 8 days ago
Job description
ClariMed is seeking a Participant Recruitment & Study Startup Manager to oversee participant recruitment and study startup activities for our human factors research studies. This role is responsible for ensuring studies are operationally prepared, participant recruitment goals are achieved, and study timelines stay on track from planning through study launch.
This position is focused on recruiting participants for research studies and is not an employee recruiting, talent acquisition, or staffing role.
The Participant Recruitment & Study Startup Manager will serve as a key operational leader, partnering closely with project managers, teams, and clients to ensure studies are successfully planned, staffed with qualified participants, and executed on schedule. This individual will oversee the participant recruitment function, provide leadership to the recruitment team, and continuously improve recruitment strategies, study startup processes, and operational efficiency.
This is an on-site position based in Chadds Ford, Pennsylvania.
Participant Recruitment- Lead participant recruitment efforts across multiple concurrent human factors research studies.
- Develop recruitment strategies based on study objectives, participant profiles, timelines, and enrollment goals.
- Oversee participant sourcing, outreach, pre-screening, scheduling, and enrollment.
- Ensure recruitment goals are met while maintaining a positive participant experience.
- Monitor recruitment metrics and adjust strategies to address enrollment challenges.
- Build and maintain relationships with participant databases, community organizations, recruitment partners, and other sourcing channels.
- Ensure participant records are accurate, organized, and maintained in accordance with company procedures and applicable privacy requirements.
- Identify opportunities to improve recruitment processes, tools, and participant engagement.
- Partner with project leads and teams during study startup to understand study requirements and operational needs.
- Develop recruitment timelines and startup plans to support successful study execution.
- Coordinate participant recruitment activities with overall study schedules.
- Ensure recruitment readiness before study launch.
- Identify operational risks and proactively recommend solutions to keep studies on schedule.
- Collaborate across departments to ensure smooth communication and execution throughout the startup process.
- Provide day-to-day leadership, coaching, and support to participant recruitment team members.
- Prioritize workload across multiple studies and allocate recruitment resources effectively.
- Establish performance expectations and provide ongoing coaching and feedback.
- Assist with hiring, onboarding, and training new recruitment team members.
- Foster a collaborative, positive, and accountable team environment.
- Develop standardized recruitment processes and best practices to support future growth.
- Recommend improvements to staffing, workflows, systems, and operational efficiency.
- Work closely with project leads, teams, clients, and other internal stakeholders throughout the study lifecycle.
- Maintain a high level of organization while managing multiple priorities in a fast-paced environment.
- Prepare recruitment updates and communicate study progress to internal teams.
- Support continuous improvement initiatives that enhance study startup, participant recruitment, and operational effectiveness.
- Perform other related duties as assigned.
- Experience in participant recruitment, human factors research, clinical research, market research, research operations, study coordination, or a related field.
- Previous leadership or management experience preferred.
- Experience managing multiple projects, priorities, and deadlines simultaneously.
- Strong organizational, planning, and problem-solving skills.
- Excellent written and verbal communication skills.
- Strong interpersonal skills with the ability to build relationships with participants, clients, and internal teams.
- Ability to think strategically while remaining hands-on in day-to-day operations.
- Experience developing recruitment strategies for diverse participant populations.
- Comfortable working in a collaborative, fast-paced environment with changing priorities.
- Experience with participant databases, CRM systems, scheduling platforms, or research management software is a plus.
- A passion for creating exceptional participant experiences.
- The ability to anticipate challenges and develop creative solutions.
- Strong leadership skills with a collaborative, team-first mindset.
- A continuous improvement mentality and desire to build scalable processes.
- A proactive, organized approach with exceptional attention to detail.