Remote Jobs at Worldwide Clinical Trials
Find your next remote opportunity · 22 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 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.
Senior Clinical Trial Liaison – Oncology
Senior Clinical Trial Liaison guiding oncology trial strategy and site engagement for Worldwide Clinical Trials, a global contract research organization. Supporting feasibility, recruitment, proposals, and business development.
Regulatory Affairs Specialist – German Speaker
Regulatory Affairs Specialist ensuring regulatory compliance and submissions for clinical trials in Germany and Switzerland. Collaborating with internal teams and external regulators while managing documentation.
Site Contracts Lead, Europe
Site Contracts Lead overseeing clinical trial agreements and mentoring specialists. Collaborating with internal and external stakeholders to manage contracting processes efficiently.
In-House Clinical Research Associate
Clinical Research Associate ensuring data quality and regulatory compliance for clinical trials. Engaging with diverse teams to facilitate efficient execution of studies and support patient care.
Senior Clinical Research Associate – Oncology
Senior Clinical Research Associate managing oncology trials while leading site management activities remotely for Worldwide Clinical Trials. Collaborating on research across diverse therapeutic areas within a global team.
Pharmacovigilance Specialist
Pharmacovigilance Specialist managing SAE data collection and reporting at Worldwide Clinical Trials. Ensuring regulatory compliance in a dynamic, global environment with a focus on patient safety.
Senior Statistician
Senior Statistician providing statistical consultancy and managing statistical support for clinical trials at Worldwide Clinical Trials. Leading design and analysis for multiple clinical projects.
Senior Director of Clinical Projects, Clinical Assessment Technologies
Director of Clinical Projects overseeing clinical activities and leading initiatives for Worldwide Clinical Trials. Responsible for mentoring teams and ensuring compliance with guidelines while driving improvements.
Senior Clinical Trials Associate
Senior Clinical Trials Associate providing administrative support to clinical project teams at Worldwide Clinical Trials. Focusing on documentation quality control and team coordination responsibilities.
Project Manager – Oncology
Project Manager coordinating and managing clinical trials from start-up to closeout at Worldwide Clinical Trials. Ensuring project deliverables meet cost, quality, and time expectations while collaborating across teams.