Corporate SGA - HOUSTON, TX 77064 The Study Start-Up (SSU) Manager is responsible for overseeing and driving operational study startup activities across the clinical research network from study award ...
Corporate SGA - HOUSTON, TX 77064 The Study Start-Up (SSU) Manager is responsible for overseeing and driving operational study startup activities across the clinical research network from study award ...
The Study Start-Up (SSU) Manager is responsible for overseeing and driving operational study startup activities across the clinical research network from study award through activation. This role ...
The Study Start-Up (SSU) Manager is responsible for overseeing and driving operational study startup activities across the clinical research network from study award through activation. This role ...
The Study Start-Up (SSU) Manager is responsible for overseeing and driving operational study startup activities across the clinical research network from study award through activation. This role ...
The Study Start-Up (SSU) Manager is responsible for overseeing and driving operational study startup activities across the clinical research network from study award through activation. This role ...
Study Start-Up Lead, APAC
Pacific, MO · On-site
$150 - $200/hr
Minimum 5 years of clinical research experience, with 2+ years in SSU or regulatory submissions, including CTIS experience. * Strong understanding of global and local regulatory requirements.
Study Start-Up Lead, APAC
Pacific, MO · On-site
$150 - $200/hr
Minimum 5 years of clinical research experience, with 2+ years in SSU or regulatory submissions, including CTIS experience. * Strong understanding of global and local regulatory requirements.
$150 - $200/hr
Minimum 5 years of clinical research experience, with 2+ years in SSU or regulatory submissions, including CTIS experience. * Strong understanding of global and local regulatory requirements.
$150 - $200/hr
Minimum 5 years of clinical research experience, with 2+ years in SSU or regulatory submissions, including CTIS experience. * Strong understanding of global and local regulatory requirements.
Premier Research is looking for a Senior Clinical Research Associate, Neuroscience (Contract) to join our Clinical Monitoring, Site Management and SSU team. You will help biotech, medtech, and ...
Premier Research is looking for a Senior Clinical Research Associate, Neuroscience (Contract) to join our Clinical Monitoring, Site Management and SSU team. You will help biotech, medtech, and ...
... research professional responsible for supporting and driving key operational activities across Clinical Operations, Study Start-Up (SSU), Trial Master File (TMF) Management, Data Management, Vendor ...
... research professional responsible for supporting and driving key operational activities across Clinical Operations, Study Start-Up (SSU), Trial Master File (TMF) Management, Data Management, Vendor ...
Premier Research is looking for a Senior Clinical Research Associate, Neuroscience (Contract) to join our Clinical Monitoring, Site Management and SSU team. You will help biotech, medtech, and ...
Premier Research is looking for a Senior Clinical Research Associate, Neuroscience (Contract) to join our Clinical Monitoring, Site Management and SSU team. You will help biotech, medtech, and ...
... research professional responsible for supporting and driving key operational activities across Clinical Operations, Study Start-Up (SSU), Trial Master File (TMF) Management, Data Management, Vendor ...
... research professional responsible for supporting and driving key operational activities across Clinical Operations, Study Start-Up (SSU), Trial Master File (TMF) Management, Data Management, Vendor ...
Clinical Operations Associate (Pool)
CA · Remote
$70K - $80K/yr
Vanguard Clinical, Inc. is a Contract Research Organization (CRO) headquartered in San Diego, CA ... Study Start-Up (SSU) Support * Support collection, tracking, and review of essential documents ...
Clinical Operations Associate (Pool)
CA · Remote
$70K - $80K/yr
Vanguard Clinical, Inc. is a Contract Research Organization (CRO) headquartered in San Diego, CA ... Study Start-Up (SSU) Support * Support collection, tracking, and review of essential documents ...
Clinical Study Administrator
Wilmington, DE · On-site
$93K - $139K/yr
The SSU CSA works under the guidance of the SSU Manager to support timely site activation while ... Experience: 1-3 years of relevant experience in clinical research, study start-up, or regulated ...
Clinical Study Administrator
Wilmington, DE · On-site
$93K - $139K/yr
The SSU CSA works under the guidance of the SSU Manager to support timely site activation while ... Experience: 1-3 years of relevant experience in clinical research, study start-up, or regulated ...
Study Start Up Associate II
Cary, NC · On-site
$31 - $42.50/hr
... clinical research organisation united by a mission to bring new medicines and treatments to ... Support the day-to-day operations of assigned activities within SSU to ensure completion per ...
Study Start Up Associate II
Cary, NC · On-site
$31 - $42.50/hr
... clinical research organisation united by a mission to bring new medicines and treatments to ... Support the day-to-day operations of assigned activities within SSU to ensure completion per ...
Study Start Up Associate II
Pittsburgh, PA · On-site
$32.50 - $44.50/hr
... clinical research organisation united by a mission to bring new medicines and treatments to ... Support the day-to-day operations of assigned activities within SSU to ensure completion per ...
Study Start Up Associate II
Pittsburgh, PA · On-site
$32.50 - $44.50/hr
... clinical research organisation united by a mission to bring new medicines and treatments to ... Support the day-to-day operations of assigned activities within SSU to ensure completion per ...
Study Start Up Associate II
North Wales, PA · On-site
$32.50 - $44.25/hr
... clinical research organisation united by a mission to bring new medicines and treatments to ... Support the day-to-day operations of assigned activities within SSU to ensure completion per ...
Study Start Up Associate II
North Wales, PA · On-site
$32.50 - $44.25/hr
... clinical research organisation united by a mission to bring new medicines and treatments to ... Support the day-to-day operations of assigned activities within SSU to ensure completion per ...
Clinical Study Administrator
Wilmington, DE · On-site
$93K - $139K/yr
The SSU CSA works under the guidance of the SSU Manager to support timely site activation while ... Experience: 1-3 years of relevant experience in clinical research, study start-up, or regulated ...
Clinical Study Administrator
Wilmington, DE · On-site
$93K - $139K/yr
The SSU CSA works under the guidance of the SSU Manager to support timely site activation while ... Experience: 1-3 years of relevant experience in clinical research, study start-up, or regulated ...
Manager, Clinical Operations
$110K/yr
Premier Research is looking for a Manager, Clinical Operations to join our Clinical Monitoring, Site Management and SSU team. You will help biotech, medtech, and specialty pharma companies transform ...
Manager, Clinical Operations
$110K/yr
Premier Research is looking for a Manager, Clinical Operations to join our Clinical Monitoring, Site Management and SSU team. You will help biotech, medtech, and specialty pharma companies transform ...
Clinical Study Administrator
Wilmington, DE · On-site
$93K - $139K/yr
The SSU CSA works under the guidance of the SSU Manager to support timely site activation while ... Experience: 1-3 years of relevant experience in clinical research, study start-up, or regulated ...
Clinical Study Administrator
Wilmington, DE · On-site
$93K - $139K/yr
The SSU CSA works under the guidance of the SSU Manager to support timely site activation while ... Experience: 1-3 years of relevant experience in clinical research, study start-up, or regulated ...
Clinical Lead II (Dermatology)
$116K/yr
Premier Research is looking for a Clinical Lead II (Dermatology) to join our Clinical Monitoring, Site Management and SSU team. You will help biotech, medtech, and specialty pharma companies ...
Clinical Lead II (Dermatology)
$116K/yr
Premier Research is looking for a Clinical Lead II (Dermatology) to join our Clinical Monitoring, Site Management and SSU team. You will help biotech, medtech, and specialty pharma companies ...
Study Start Up Associate II
Philadelphia, PA · On-site
$33.75 - $46.25/hr
... clinical research organisation united by a mission to bring new medicines and treatments to ... Support the day-to-day operations of assigned activities within SSU to ensure completion per ...
Study Start Up Associate II
Philadelphia, PA · On-site
$33.75 - $46.25/hr
... clinical research organisation united by a mission to bring new medicines and treatments to ... Support the day-to-day operations of assigned activities within SSU to ensure completion per ...
NY · On-site
$110K/yr
About Premier Research Premier Research is looking for a Manager, Clinical Operations to join our Clinical Monitoring, Site Management and SSU team. You will help biotech, medtech, and specialty ...
NY · On-site
$110K/yr
About Premier Research Premier Research is looking for a Manager, Clinical Operations to join our Clinical Monitoring, Site Management and SSU team. You will help biotech, medtech, and specialty ...
Clinical Research Ssu information
See salary details
$36K - $45.8K
8% of jobs
$45.8K - $55.5K
8% of jobs
$60.4K is the 25th percentile. Wages below this are outliers.
$55.5K - $65.3K
17% of jobs
$65.3K - $75.1K
10% of jobs
$75.1K - $84.9K
3% of jobs
The median wage is $94.6K / yr.
$84.9K - $94.6K
3% of jobs
$94.6K - $104.4K
6% of jobs
$104.4K - $114.2K
8% of jobs
$114.2K - $124K
7% of jobs
$125.3K is the 75th percentile. Wages above this are outliers.
$124K - $133.7K
23% of jobs
$133.7K - $143.5K
5% of jobs
$36K
$94.3K
$143.5K
How much do clinical research ssu jobs pay per year?
What does a clinical research SSU do?
What are some common challenges faced by clinical research SSU professionals during study start-up, and how can they be managed?
What are the key skills and qualifications needed to thrive as a clinical research SSU specialist, and why are they important?
What is the difference between Clinical Research Ssu vs Clinical Research Coordinator?
| Aspect | Clinical Research Ssu | Clinical Research Coordinator |
|---|---|---|
| Certifications | Often requires GCP training, basic research certifications | Typically requires GCP training, research certifications |
| Work Environment | Supports clinical trials, often in hospitals or research centers | Manages daily trial activities, in clinics or research sites |
| Employer & Industry | Pharmaceutical companies, CROs, hospitals | Academic institutions, hospitals, research sites |
Both roles involve supporting clinical trials and require similar certifications. However, Clinical Research SSUs often focus on data management and regulatory support, while Clinical Research Coordinators handle patient interactions and trial logistics. Understanding these differences helps in choosing the right career path or job search focus.
What are popular job titles related to Clinical Research Ssu jobs?
For Clinical Research Ssu jobs, the most frequently searched job titles are:

Study Start-Up (SSU) Manager (4145)
Houston, TX • On-site
Other
Posted 23 days ago
Job description
Job Location: Corporate SGA - HOUSTON, TX 77064
The Study Start-Up (SSU) Manager is responsible for overseeing and driving operational study startup activities across the clinical research network from study award through activation. This role ensures startup timelines, deliverables, dependencies, and cross-functional activities remain aligned to support efficient, compliant, and scalable study activation.
The Study Start-Up Manager serves as the primary operational lead for startup execution, coordinating closely with Regulatory, Clinical Operations, Clinical Data, sponsors, CROs, investigators, and site teams to maintain startup momentum and proactively address barriers impacting activation timelines. This role is responsible for startup performance oversight, milestone management, issue escalation, operational reporting, and process optimization to ensure consistent startup execution across the network.
DUTIES & RESPONSIBILITIES- Study Start-Up Operations & Activation Management
- Oversee and coordinate operational startup activities across assigned studies and network sites
- Drive startup timelines from study award through Site Initiation Visit (SIV) and activation readiness
- Maintain oversight of startup milestones, dependencies, deliverables, and critical path activities
- Ensure startup activities progress according to sponsor expectations and internal timelines
- Coordinate activation readiness across sites, vendors, sponsors, and internal departments
- Maintain startup trackers, activation reports, and milestone documentation
- Escalate delays, risks, or operational barriers impacting startup timelines
- Cross-Functional Startup Coordination
- Coordinate closely with Regulatory, Clinical Operations, Clinical Data, PMO, and site teams throughout the startup lifecycle
- Ensure alignment between regulatory progress, operational readiness, and sponsor deliverables
- Facilitate startup meetings, milestone reviews, and escalation discussions
- Maintain clear communication across stakeholders regarding startup progress, risks, and priorities
- Partner with startup stakeholders to proactively resolve operational gaps or delays
- Coordinate sponsor, CRO, vendor, and site communications related to startup activities
- Startup Performance Oversight & Reporting
- Monitor startup KPIs, activation timelines, and milestone adherence across studies and sites
- Identify startup bottlenecks, workflow inefficiencies, and operational risks impacting activation
- Track pending items, aging deliverables, outstanding approvals, and startup dependencies
- Provide regular startup status reports, escalation summaries, and operational updates to leadership
- Ensure startup reporting accuracy and visibility across systems and operational dashboards
- Support forecasting and startup pipeline visibility across the network
- Risk Management & Escalation
- Identify and proactively address startup risks, delays, and operational barriers
- Escalate critical startup concerns impacting activation timelines or sponsor expectations
- Collaborate with stakeholders to develop mitigation strategies and action plans
- Monitor issue resolution timelines and ensure appropriate follow-through
- Support operational readiness and startup quality standards across all assigned studies
- Process Optimization & Standardization
- Support continuous improvement of startup workflows, operational processes, and activation practices
- Assist with the development and maintenance of startup guidance documents, trackers, and workflow tools
- Promote consistency in startup execution, communication, and reporting practices across the network
- Support onboarding and training initiatives for startup staff and operational stakeholders
- Participate in process improvement initiatives focused on activation efficiency and operational scalability
- Team Development, Training & Operational Readiness
- Support onboarding and operational training of new SSU team members
- Reinforce standardized startup workflows, escalation pathways, and operational expectations across the team
- Provide ongoing coaching and guidance related to startup processes, systems, sponsor expectations, and activation workflows
- Identify training gaps and operational development needs impacting startup execution or performance
- Promote accountability, consistency, and operational excellence within the SSU function
- Assist with the development and maintenance of startup training materials, process guides, and workflow documentation
- Other Duties
- Perform additional operational or leadership responsibilities as assigned by management
- Preferred: Bachelor's degree in Business Administration, Healthcare Administration, Life Sciences, or a related field
- An equivalent combination of operational experience and clinical research education may also be considered
- 5+ years of clinical research experience required
- 3+ years of direct experience in Study Start-Up, Site Activation, Clinical Operations coordination, or Regulatory startup support required
- Experience managing startup timelines, activation milestones, and cross-functional operational workflows required
- Experience working within a clinical research site network, CRO, sponsor, or multi-site research environment preferred
- Prior experience coordinating across Regulatory, Clinical Operations, sponsors, CROs, and site teams preferred
- Experience managing multiple concurrent studies and startup priorities in a fast-paced operational environment is required
- Previous experience in onboarding, training, or mentoring startup staff preferred
- ACRP, SOCRA, PMP or related clinical research/project management certification preferred
- Strong understanding of clinical trial startup workflows and site activation processes
- Working knowledge of IRB/EC processes, regulatory documentation, and essential startup requirements
- Strong operational coordination and project management capabilities
- Ability to manage multiple studies, competing priorities, and aggressive startup timelines simultaneously
- Strong organizational, analytical, and problem-solving skills
- Ability to identify operational risks, bottlenecks, and timeline impacts proactively
- Excellent verbal and written communication skills
- Strong stakeholder management and cross-functional collaboration abilities
- Ability to lead startup discussions, escalation meetings, and operational follow-up effectively
- Experience with CTMS, startup trackers, eRegulatory systems, or operational workflow platforms preferred
- Strong proficiency with Microsoft Office Suite, Google Workspace, reporting tools, and operational dashboards
- Ability to function effectively in a fast-paced, evolving, and metrics-driven operational environment
- Ability to coach and support team members while promoting accountability and operational consistency
- Site Selection to Site Initiation Visit (SIV) Timeline: less than/equal to 15–20 days
- SIV to First Patient First Visit (FPFV): less than/equal to 30–45 days
- Startup Milestone Adherence: greater than/equal to 90%
- On-Time Study Activation Rate: greater than/equal to 90%
- Startup Timeline Variance Across Sites: less than/equal to 15%
- Activation Readiness Prior to SIV: greater than/equal to 90%
- Essential Startup Deliverables Completed Prior to Activation: 100%
- Outstanding Startup Dependency Aging: less than/equal to 5 business days
- Startup Escalation Resolution Timeliness: less than/equal to 2 business days
- Cross-Functional Follow-Up Completion Rate: greater than/equal to 95%
- Startup Tracker/Data Accuracy: greater than/equal to 98%
- Reporting Timeliness & Status Update Compliance: greater than/equal to 95%
- Startup Risk Identification & Escalation Compliance: greater than/equal to 95%
- Sponsor/CRO Startup Communication Responsiveness: less than/equal to 1 business day average response time
- SOP/Workflow Adherence Across Startup Activities: greater than/equal to 95%
- New Team Member Onboarding & Training Completion: 100% within designated onboarding timeline
- Startup Process Deviation Reduction Year Over Year
- Team Task Accountability & Milestone Follow Through: greater than/equal to 95%