Remote Jobs at Worldwide Clinical Trials
Find your next remote opportunity · 32 Open Positions
Worldwide Clinical Trials (Worldwide) is a full-service global contract research organization (CRO) that works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality.
Worldwide’s capabilities include bioanalytical laboratory services, Phase I-IV clinical trials, and post-approval and real-world evidence studies – all powered by an accessible team of clinicians, scientists, and researchers who bring first-hand expertise and a collaborative, personalized approach to each clinical program.
Worldwide is therapeutically focused on neuroscience, oncology, rare disease, cardiometabolic, and immune-mediated inflammatory diseases.
Its global footprint spans over 60 countries with more than 3,500 team members.
For more information on Worldwide, visit www.worldwide.com.
Senior Clinical Research Associate – Oncology
Senior Clinical Research Associate monitoring UK oncology clinical-trial sites for global CRO Worldwide Clinical Trials. Leading site activities, CRA coordination, compliance, and study delivery.
Senior Clinical Research Associate – Oncology
Senior Clinical Research Associate monitoring oncology clinical trials for global CRO Worldwide Clinical Trials in Germany. Leading site activities, mentoring CRAs, and ensuring GCP-compliant study delivery.
Senior Business Analyst, AI Evaluation – Value Realization
Senior Business Analyst evaluating AI proof-of-concept value for Worldwide Clinical Trials, a global clinical research CRO. Building evidence-based investment recommendations across regulated operations.
Senior Statistical Programmer 2
Senior Statistical Programmer leading SAS and CDISC clinical trial programming for Worldwide Clinical Trials, a global clinical research organization. Delivering regulatory-ready datasets, analyses, and submission documentation for complex studies.
Principal Statistician
Principal Biostatistician leading clinical trial design, analysis, and reporting for global CRO Worldwide Clinical Trials. Providing statistical leadership, sponsor consultation, and mentorship across regulated research studies.
Senior Clinical Research Associate – CNS
Senior Clinical Research Associate monitoring CNS clinical trials across Czechia for Worldwide Clinical Trials, a global contract research organization. Managing sites, compliance, data quality, and study closeout.
Clinical Innovation Executive Director
Clinical innovation executive directing AI, automation, and digital transformation for Worldwide Clinical Trials, a global CRO. Building scalable clinical-development solutions, governance, and measurable business value.
Associate II, TMF Operations – LATAM
TMF Operations Associate maintaining inspection-ready clinical trial documents for Worldwide Clinical Trials, a global CRO. Reviewing, indexing, and quality-controlling TMF records across sponsor studies.
Manager, Clinical Database Programming
Clinical database programming manager leading teams and EDC delivery for Worldwide Clinical Trials, a global CRO. Overseeing database configuration, validation, quality, and clinical data workflows.
Site Contracts Specialist
Site Contracts Specialist negotiating and executing clinical trial agreements for Worldwide Clinical Trials, a global CRO. Managing budgets, compliance, risks, and study-startup timelines with clinical sites and sponsors.
Senior Manager, Organizational Learning & Talent Enablement
Senior manager overseeing learning operations, compliance training, performance management, and talent enablement at global CRO Worldwide Clinical Trials. Leading teams, governance, and enterprise stakeholder partnerships.
PRN Data Coordinator
Part-time remote Data Coordinator transcribing clinical-trial source data into accurate Case Report Forms. Supporting document tracking, reconciliation, and Good Clinical Practice compliance at Worldwide Clinical Trials.
Senior Specialist
Senior Site Contracts Specialist negotiating clinical trial agreements, budgets, and amendments for Worldwide Clinical Trials, a global clinical research organization. Managing site contracting risks, compliance, and execution.
Senior Clinical Research Associate
Senior Clinical Research Associate overseeing site qualification, monitoring, compliance, and close-out activities. Supporting Worldwide Clinical Trials’ global CRO studies in South Korea.
Clinical Research Associate – Neurology, Oncology
Clinical Research Associate managing neurology and oncology trial sites for Worldwide Clinical Trials, a global CRO. Conducting monitoring, compliance, safety, and data-quality activities remotely in Bulgaria.
Senior Site Activation Manager
Senior Site Activation Manager overseeing clinical trial site activation and start-up for Worldwide Clinical Trials, a global CRO. Managing documents, contracts, regulatory activities, and project delivery.
Investigator – Grants Specialist
Investigator Grants Specialist developing and forecasting investigator grants for Worldwide Clinical Trials, a global CRO. Reviewing protocols, budgets, fair-market-value benchmarks, and regulatory requirements.
Project Manager, Internal Medicine
Project Manager leading Phase I–IV clinical trials for global CRO Worldwide Clinical Trials. Coordinating teams, resources, deliverables, and regulatory-compliant execution.
In-House Clinical Research Associate II
In-house Clinical Research Associate supporting site management and data-quality activities for Worldwide Clinical Trials, a global contract research organization. Coordinating clinical-study documentation, monitoring support, queries, recruitment, and site communications.
Investigator, Grants Specialist
Investigator Grants Specialist forecasting and costing clinical-trial grants for Worldwide Clinical Trials, a global CRO. Collaborating across commercial, project, clinical, and site-activation teams.