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Temporary Contract Clinical Data Manager Jobs (NOW HIRING)

Eliassen Group

Clinical Data Manager

Chicago, IL · On-site +1

$50 - $60/hr

This is a 1-year contract with potential extension and will operate remotely with optional hybrid ... Lead clinical data management for an assigned cardiovascular trial in alignment with SOPs, GCP, and ...

Pharmaron

Clinical Data Manager

Somerset, NJ · On-site

$60K - $75K/yr

Clinical Data Manager FLSA Status: Exempt Location ... Onsite (Somerset, New Jersey) Salary: $60,000 - $75,000 Pharmaron is a global CRO (Contract ...

Sumitomopharma

OR · On-site

$130K - $163K/yr

Execute and manage all in house clinical data management activities for assigned oncology trials in accordance with ICH/GCP, regulatory requirements, and internal SOPs. * Support and contribute to ...

CYNET SYSTEMS

Clinical Data Manager

Sunnyvale, CA · On-site

$70 - $75/hr

Support clinical data review requirements from Lead data manager. * Create customise data review listings for study per specifications from lead data manager. * Provide clinical data management ...

Sumitomo Pharma

Clinical Data Manager

$130K - $163K/yr

Execute and manage all in house clinical data management activities for assigned oncology trials in accordance with ICH/GCP, regulatory requirements, and internal SOPs. * Support and contribute to ...

Faeth Therapeutics

Clinical Data Manager

San Francisco, CA · On-site

$125K - $175K/yr

Faeth Therapeutics is seeking an experienced Clinical Data Manager to support clinical data management activities across two active clinical trials. This individual will play a critical role in ...

Ceribell, Inc

Clinical Data Manager

Sunnyvale, CA · On-site

$190K - $200K/yr

The Clinical Data Manager is the technical lead for clinical data management, accountable for designing and governing end-to-end data strategies to ensure high quality, clinical data across multiple ...

Ceribell, Inc

Clinical Data Manager

Palo Alto, CA

$190K - $200K/yr

The Clinical Data Manager is the technical lead for clinical data management, accountable for designing and governing end-to-end data strategies to ensure high quality, clinical data across multiple ...

Ceribell, Inc

Clinical Data Manager

Santa Clara, CA

$190K - $200K/yr

The Clinical Data Manager is the technical lead for clinical data management, accountable for designing and governing end-to-end data strategies to ensure high quality, clinical data across multiple ...

Ceribell, Inc

Clinical Data Manager

Sunnyvale, CA

$190K - $200K/yr

The Clinical Data Manager is the technical lead for clinical data management, accountable for designing and governing end-to-end data strategies to ensure high quality, clinical data across multiple ...

Ceribell, Inc

Clinical Data Manager

San Jose, CA

$190K - $200K/yr

The Clinical Data Manager is the technical lead for clinical data management, accountable for designing and governing end-to-end data strategies to ensure high quality, clinical data across multiple ...

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How much do temporary contract clinical data manager jobs pay per hour?

As of Jun 11, 2026, the average hourly pay for temporary contract clinical data manager in the United States is $57.17, according to ZipRecruiter salary data. Most workers in this role earn between $45.19 and $68.03 per hour, depending on experience, location, and employer.

What are Temporary Contract Clinical Data Managers?

Temporary Contract Clinical Data Managers are professionals hired on a short-term basis to oversee the collection, management, and quality assurance of clinical trial data. They ensure that the data from clinical studies is accurate, complete, and compliant with regulatory standards. These roles are often project-based and may involve tasks such as designing data collection systems, monitoring data integrity, and preparing reports for regulatory submissions. Temporary contracts allow organizations to meet fluctuating project needs without committing to permanent hires.

What are some common challenges faced by Temporary Contract Clinical Data Managers, and how can they prepare to address them?

Temporary Contract Clinical Data Managers often face the challenge of quickly adapting to new systems, processes, and team dynamics within a short timeframe. They are expected to efficiently manage clinical trial data, ensure data quality, and adhere to strict regulatory standards despite limited onboarding. To succeed, it's helpful to familiarize oneself with common clinical data management platforms, maintain strong organizational skills, and be proactive in communicating with study teams. Building rapport with key colleagues early on can also help navigate project-specific requirements and ensure smooth collaboration.

What is the difference between Temporary Contract Clinical Data Manager vs Clinical Data Coordinator?

AspectTemporary Contract Clinical Data ManagerClinical Data Coordinator
CredentialsBachelor's degree in life sciences, experience with clinical data systemsBachelor's degree, familiarity with data entry and management
Work EnvironmentContract-based, often in pharmaceutical or biotech companiesFull-time, in clinical research teams or CROs
Employer & IndustryPharmaceutical, biotech, CROsResearch sites, CROs, pharmaceutical companies
Search & Comparison IntentUnderstanding contract roles, data management tasksData entry, coordination, and support roles

The Temporary Contract Clinical Data Manager typically oversees data management during clinical trials on a contract basis, focusing on data quality and compliance. In contrast, a Clinical Data Coordinator handles data entry and coordination tasks within ongoing studies. Both roles require similar credentials but differ mainly in scope, duration, and responsibilities.

What are the key skills and qualifications needed to thrive as a Temporary Contract Clinical Data Manager, and why are they important?

To thrive as a Temporary Contract Clinical Data Manager, you need expertise in clinical data management, data integrity, and regulatory compliance, usually supported by a degree in life sciences or a related field. Proficiency with data management systems such as Medidata Rave, Oracle Clinical, and knowledge of CDISC standards, along with relevant certifications like Society for Clinical Data Management (SCDM), is commonly required. Strong attention to detail, problem-solving, and effective communication are crucial soft skills for collaborating with cross-functional teams and ensuring high-quality data. These skills and qualifications are essential to ensure accurate, timely, and compliant management of clinical trial data, directly impacting the success of clinical research projects.
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Temporary Contract Clinical Data Manager jobs near you
Clinical Data Manager

Clinical Data Manager

Trident Consulting Inc

Aliso Viejo, CA • On-site

Full-time

This job post has expired 2 days ago. Applications are no longer accepted.

Job description

Company Description

About Trident:
Trident Consulting is an award-winning IT/engineering staffing company founded in 2005 and headquartered in San Ramon, CA. We specialize in placing high-quality vetted technology
Some of our recent awards include:
2022, 2021, 2020 Inc. 5000 fastest-growing private companies in America
2022, 2021 SF Business Times 100 fastest-growing private companies in Bay Area

Job Description

Trident Consulting is currently seeking a Clinical Data Manager for one of our industry leading clients.

Role: Clinical Data Manager II

Location: Aliso Viejo, CA - Onsite
Duration: 6 Months
Shift: 1st Shift
Employment Type: Temporary / Contract

Pay: $26/hr - $29/hr on W2(Inclusive all)

Position Summary

Client is seeking an experienced Clinical Data Manager II to support clinical study data management activities from study startup through study closeout. This role will be responsible for ensuring the quality, integrity, and compliance of clinical trial data while collaborating closely with cross-functional clinical teams. The ideal candidate will have hands-on experience in clinical data management, EDC systems, data review, and regulatory compliance within pharmaceutical, biotechnology, medical device, or CRO environments.

Key Responsibilities

  • Author, review, and maintain Data Management documentation, including:
    • Data Management Plans (DMPs)
    • Project Plans
    • CRF Completion Guidelines
    • Edit Check Specifications
    • Data Review Guidelines
  • Coordinate and execute User Acceptance Testing (UAT) activities for clinical databases and EDC systems.
  • Facilitate Data Management meetings with Clinical Operations, Project Management, Programming, Regulatory Affairs, and Study Teams.
  • Manage EDC study deliverables and support database management activities.
  • Lead ongoing data cleaning and query management efforts.
  • Review clinical data for trends, inconsistencies, quality issues, and outliers.
  • Generate, track, and resolve data queries.
  • Provide study data status updates, metrics, and reporting to stakeholders.
  • Review SAS and SDTM datasets to ensure data quality and regulatory compliance.
  • Support external data reconciliation and third-party vendor data review.
  • Collaborate with programming teams to create custom reports, listings, and data review outputs.
  • Support medical coding and AE/SAE reconciliation activities.
  • Maintain audit-ready Data Management documentation.
  • Monitor study enrollment and provide enrollment metrics.
  • Assist in developing training materials for investigators, clinical sites, and internal teams.
  • Contribute to process improvements, SOP development, and best practices within Data Management.

Required Qualifications

  • 2–5 years of Clinical Data Management experience.
  • Experience within Pharmaceutical, Biotechnology, Medical Device, or CRO environments.
  • Strong knowledge of FDA, ICH-GCP, and clinical data management regulations and guidelines.
  • Hands-on experience with Electronic Data Capture (EDC) systems such as:
    • Medidata RAVE
    • Oracle Inform
    • iMedNet
    • Similar EDC platforms
  • Experience with clinical database design concepts and data review tools.
  • Knowledge of CDISC standards including CDASH and SDTM.
  • Experience writing and maintaining Data Management documentation.
  • Experience with data review, query management, and reconciliation processes.
  • Strong project coordination, organizational, and analytical skills.
  • Excellent verbal and written communication skills.
  • Experience with SAS, SQL, Excel, or related data analysis tools is a plus.
  • Bachelor's degree or higher in Biological Sciences, Nursing, Healthcare, or a related discipline preferred.

Preferred Qualifications

  • Ophthalmology clinical research experience.
  • Medical device clinical trial experience.
  • Experience supporting regulatory submissions and inspection readiness activities.

Required Skills

  • Clinical Data Management
  • Electronic Data Capture (EDC) Systems
  • Medidata RAVE / Oracle Inform / iMedNet
  • UAT Testing
  • Data Cleaning & Validation
  • Query Management
  • CDISC Standards (CDASH, SDTM)
  • SAS and SQL
  • Clinical Trial Documentation
  • Regulatory Compliance (FDA, ICH-GCP)
  • Medical Coding & Reconciliation
  • Cross-Functional Collaboration
  • Project Coordination & Reporting

Nice-to-Have Skills

  • Ophthalmology Studies
  • Medical Device Clinical Trials
  • External Data Reconciliation
  • Safety Data Review
  • Clinical Reporting & Metrics Generation
Additional Information

All your information will be kept confidential according to EEO guidelines.

Trident Consulting logo

About Trident Consulting

Sourced by ZipRecruiter

Trident Consulting is a certified 100% woman- and minority-owned staffing company, incorporated in 2005. Some of our achievements include making it to the Inc. 5000 list and Bay Area's list of Top 100 fastest growing companies.

Industry

It services

Company size

51 - 200 Employees

Headquarters location

Dublin, CA, US

Year founded

2005

Social media

Twitter

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