1

Clinical Data Coordinator Jobs in Spring, TX (NOW HIRING)

Be Seen First

Clinical Research Coordinator (CRC) Kingwood, Texas | On-site We are seeking a motivated and detail ... Perform clinical assessments and collect study data * Assist with and support surgical procedures ...

Be Seen First

Clinical Research Coordinator (CRC) Kingwood, Texas | On-site We are seeking a motivated and detail ... Perform clinical assessments and collect study data * Assist with and support surgical procedures ...

Clinical Research Coordinator II

Houston, TX

$23.25 - $30.75/hr

Documentation * Record data legibly and enter in real time on paper or e-source documents ... Minimum Experience: * 3 years prior Clinical Research Coordinator experience required * Prefer 1 ...

Clinical Research Coordinator II

Houston, TX · On-site

$23.25 - $30.75/hr

Help ensure participant safety and the integrity and quality of clinical trial data. * Participate ... Experience coordinating clinical trials and working directly with research participants. * Working ...

Clinical Research Coordinator II

Bellaire, TX · On-site

$21.75 - $29/hr

Help ensure participant safety and the integrity and quality of clinical trial data. * Participate ... Experience coordinating clinical trials and working directly with research participants. * Working ...

Showing results 21-40

Clinical Data Coordinator information

See Spring, TX salary details

$14

$26

$50

How much do clinical data coordinator jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for clinical data coordinator in Spring, TX is $26.38, according to ZipRecruiter salary data. Most workers in this role earn between $20.34 and $30.14 per hour, depending on experience, location, and employer.

What does a clinical data coordinator do?

A Clinical Data Coordinator is responsible for collecting, managing, and ensuring the quality of data generated from clinical trials and medical research studies. They work closely with clinical research teams to input, verify, and monitor data accuracy, integrity, and compliance with regulatory standards. Their work is vital for the successful analysis of clinical trial outcomes and for supporting the development of new medical treatments.

What does a clinical data coordinator do?

A clinical data coordinator is responsible for overseeing a number of data related tasks associated with running a clinical facility. In this career, your job duties include creating reports on patient data, developing programs that support a clinical study, and providing information to ensure regulatory compliance on behalf of the clinic. The qualifications needed to have a career as a clinical data coordinator include a bachelor's degree in computer science or a related field. You also need strong analytical skills and experience working with databases.

How does a clinical data coordinator typically collaborate with other teams during a clinical trial?

Clinical Data Coordinators work closely with clinical research associates, data managers, and regulatory teams to ensure the accurate collection and management of trial data. They frequently communicate with site staff to resolve data discrepancies and ensure adherence to protocol and data quality standards. Regular meetings and updates are common to address ongoing data queries, share progress, and align on timelines. This cross-functional collaboration is vital for maintaining the integrity of clinical trial data and supporting successful study outcomes.

What are the key skills and qualifications needed to thrive as a clinical data coordinator, and why are they important?

To thrive as a Clinical Data Coordinator, you need strong analytical skills, attention to detail, and a background in life sciences or a related field, often supported by a bachelor’s degree. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) tools, and knowledge of regulatory standards such as GCP and FDA guidelines are essential. Excellent organizational skills, effective communication, and the ability to collaborate with multidisciplinary teams help set top candidates apart. These competencies ensure accurate data collection and integrity, which are crucial for the success and compliance of clinical trials.

What is the difference between Clinical Data Coordinator vs Clinical Research Associate?

AspectClinical Data CoordinatorClinical Research Associate
Primary RoleManage and ensure accuracy of clinical data collection and entryOversee clinical trial sites, monitor study progress, and ensure compliance
Required CredentialsTypically a bachelor's degree in health, life sciences, or related fieldUsually a bachelor's degree in health sciences, along with monitoring certifications
Work EnvironmentData management teams, clinical trial databases, research organizationsClinical sites, monitoring visits, regulatory agencies
Industry UsageCommon in clinical data management and research organizationsCommon in pharmaceutical companies and contract research organizations

The Clinical Data Coordinator focuses on managing and verifying clinical data accuracy, while the Clinical Research Associate monitors trial sites and ensures compliance. Both roles are essential in clinical research but differ in daily responsibilities and focus areas.

What are the most commonly searched types of Clinical Data jobs in Spring, TX?

The most popular types of Clinical Data jobs in Spring, TX are:

What are popular job titles related to Clinical Data Coordinator jobs in Spring, TX?

For Clinical Data Coordinator jobs in Spring, TX, the most frequently searched job titles are:

What job categories do people searching Clinical Data Coordinator jobs in Spring, TX look for?

The top searched job categories for Clinical Data Coordinator jobs in Spring, TX are:

What cities near Spring, TX are hiring for Clinical Data Coordinator jobs?

Cities near Spring, TX with the most Clinical Data Coordinator job openings:

Infographic showing various Clinical Data Coordinator job openings in Spring, TX as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 12% Part Time, and 3% Contract. Highlights an 84% Physical, 4% Hybrid, and 12% Remote job distribution, with an average salary of $54,876 per year, or $26.4 per hour.

Study Start-Up (SSU) Manager (4145)

Dm Clinical Research Group

Houston, TX • On-site

$120 - $160/hr

Other

Posted 13 days ago


Job description

Job Details

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
  1. 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
  2. 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
  3. 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
  4. 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
  5. 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
  6. 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
  7. Other Duties
    • Perform additional operational or leadership responsibilities as assigned by management
KNOWLEDGE & EXPERIENCEEducation
  • 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
Experience
  • 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
Credentials
  • ACRP, SOCRA, PMP or related clinical research/project management certification preferred
Knowledge and Skills
  • 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
KPI & Success MetricsStartup Timelines & Activation Performance
  • 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%
Startup Coordination & Operational Readiness
  • 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%
Operational Oversight & Reporting
  • 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
Process Consistency & Team Performance
  • 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%
Qualifications
#J-18808-Ljbffr