GCP Quality Data Specialist

Actalent; United States; Remote; USD 76,000 - 90,000; Full time

Benefits offered by this job

Fully remote work

Medical, dental & vision

401(k) Retirement Plan

PTO / holidays

Job summary

Actalent is seeking a GCP Quality Data Specialist to provide independent QA oversight of clinical studies, review data and study documentation for quality and compliance, identify emerging GCP risks, and ensure issues are escalated, investigated, and tracked to closure. This fully remote contract-to-hire position is based out of Philadelphia, PA, with limited quarterly onsite meetings.

The hourly pay range is $55.00–$65.00, and benefits may apply during the assignment with potential conversion

Qualifications

• GCP and clinical quality compliance per ICH E6.
• Hands-on review of listings, data, eligibility, dosing, AEs and chain-of-identity.
• Protocol deviations review and trend identification.
• Inspection readiness and support for inspections.
• CROs and outsourced vendor oversight.
• TMF quality review for completeness and accuracy.
• Quality metrics and dashboards development.
• Excel, pivot tables, lookups for data analysis.
• Audit-trail reviews and data integrity support.
• Clear escalation and documentation of observations.

Responsibilities

• Perform independent, risk-based quality reviews of clinical trial data and study documentation.
• Review listings, data, eligibility, dosing, adverse events, SAEs, and chain-of-identity information.
• Review and trend protocol deviations across studies, sites, and vendors.
• Identify recurring or systemic quality risks and support CAPA development and closure.
• Build or maintain key quality indicators, dashboards, and trend reports.
• Support oversight of CROs, clinical vendors, eClinical providers, central laboratories, and specialty laboratories.
• Review data management plans, reconciliations, transfer specifications, vendor deliverables, and performance metrics.
• Conduct eTMF quality checks for completeness, timeliness, accuracy, and inspection readiness.
• Review study-related training records and identify documentation gaps.
• Support site, vendor, internal process, and regulatory inspection activities.
• Assist with inspection data requests, storyboards, data pulls, and back-room support.
• Support data-integrity assessments and audit-trail reviews.
• Contribute to SOPs, work instructions, and training associated with clinical data review and quality oversight.
• Partner with Clinical Operations, Clinical Quality, Regulatory Affairs, data-focused functions, vendors, and study stakeholders.

Skills

GCP Compliance

Clinical Data Review

Protocol Deviations

Inspection Readiness

CRO Oversight

TMF Quality

Quality Metrics

Excel Analysis

Data Integrity

Escalation Skills

Tools

Medidata Rave

Job description

Job Title: GCP Quality Data Specialist

Job Description

The GCP Clinical Quality Data Specialist will provide independent Quality Assurance oversight of clinical studies supporting the sponsor company's clinical development portfolio. The individual will review clinical data and study documentation from a quality and compliance perspective, identify emerging trends or GCP risks, and help ensure issues are appropriately escalated, investigated, corrected, and tracked to closure.

Responsibilities

• Perform independent, risk-based quality reviews of clinical trial data and study documentation.
• Review listings, data, eligibility, dosing, adverse events, serious adverse events, concomitant medications, and chain-of-identity information.
• Review and trend protocol deviations across studies, sites, and vendors.
• Identify recurring or systemic quality risks and support root-cause analysis, CAPA development, effectiveness checks, and closure.
• Build or maintain key quality indicators, dashboards, and trend reports.
• Support oversight of CROs, clinical vendors, eClinical providers, central laboratories, and specialty laboratories.
• Review data management plans, reconciliations, transfer specifications, vendor deliverables, and performance metrics.
• Conduct eTMF quality checks for completeness, timeliness, accuracy, and inspection readiness.
• Review study-related training records and identify documentation gaps.
• Support site, vendor, internal process, and regulatory inspection activities.
• Assist with inspection data requests, storyboards, data pulls, and back-room support.
• Support data-integrity assessments and audit-trail reviews.
• Contribute to SOPs, work instructions, and training associated with clinical data review and quality oversight.
• Partner with Clinical Operations, Clinical Quality, Regulatory Affairs, data-focused functions, vendors, and study stakeholders.

Essential Skills

• GCP and clinical quality compliance: Apply ICH E6 GCP principles.
• Hands-on clinical data review: Review listings, data, eligibility, dosing, concomitant medications, adverse events, serious adverse events, and chain-of-identity information.
• Protocol deviation oversight: Review deviation classification and identify trends.
• Inspection readiness: Maintain an inspection-ready state and support inspection activities.
• CRO and vendor oversight: Evaluate CROs, eClinical vendors, central laboratories, and specialty laboratories.
• TMF quality: Review eTMF for completeness, timeliness, accuracy, and overall health.
• Quality metrics and trending: Build or maintain key quality indicators, dashboards, and trend reports.
• Excel and data analysis: Use pivot tables, lookups, filters, and related functions.
• Data integrity: Support audit-trail reviews and assessments.
• Clear escalation: Document observations objectively and communicate findings.

Additional Skills & Qualifications

• At least 3 years of clinical research experience in a biotechnology, pharmaceutical, or CRO environment.
• At least 2 years in Clinical Quality Assurance, Clinical Data Management, Clinical monitoring, or Centralized monitoring.
• Working knowledge of GCP and clinical-trial requirements.
• Experience working with clinical data listings, reconciliation reports, study-level metrics, or quality data.
• Experience with CROs and outsourced clinical vendors.
• Understanding of TMF quality and inspection-readiness expectations.
• Ability to identify patterns, inconsistencies, and potential compliance risks.
• Strong written documentation and escalation skills.
• Ability to manage multiple studies and shifting priorities.
• Pivotal or registrational trial experience.
• Inspection-readiness experience.
• Experience using platforms such as Medidata Rave is preferred.
• Independent judgment rather than routine data entry or checklist-only QC.

Work Environment

This position offers a fully remote work arrangement with limited quarterly onsite exposure. Candidates may be asked to attend onsite departmental meetings approximately once per quarter in Philadelphia. The role includes holiday and PTO benefits during the contract assignment, with the potential to convert to a permanent position based on business needs and performance.

Job Type & Location

This is a Contract to Hire position based out of Philadelphia, PA.

Pay and Benefits

The pay range for this position is $55.00 - $65.00/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:Medical, dental & visionCritical Illness, Accident, and Hospital401(k) Retirement Plan Pre-tax and Roth post-tax contributions availableLife Insurance (Voluntary Life & AD&D for the employee and dependents)Short and long-term disabilityHealth Spending Account (HSA)Transportation benefitsEmployee Assistance ProgramTime Off/Leave (PTO, Vacation or Sick Leave)

Application Deadline

This position is anticipated to close on Oct 30, 2026.

Workplace Type

This is a fully remote position.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability,please email [e-mail] for other accommodation options.

San Francisco Fair Chance Ordinance

Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI)

We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.