Full-Time

Associate Project Director

Clinical Assessment Training and Surveillance

Updated on 9/4/2026

Worldwide Clinical Trials

Worldwide Clinical Trials

1,001-5,000 employees

Contract research organization delivering clinical trials

No salary listed

Remote in UK + 5 more

More locations: Alicante, Spain | Barcelona, Spain | Murcia, Spain | Madrid, Spain | Valencia, Spain

Remote

Bachelor's, Master's, MBA

Category
Biology & Biotech (1)

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Requirements
  • A minimum of a bachelor's degree.
  • Exceptional organizational, detail-oriented, and service-oriented capabilities, with strong management and supervision skills.
  • A strong understanding of best practices for clinical trial operations and rater reliability processes.
  • Knowledge of technology vendors and their capabilities.
  • Ability to plan, manage, monitor, and critique work effectively.
  • Ability to consistently meet timelines and work effectively under pressure.
  • Ability to proactively identify and escalate potential project issues to appropriate CAT and Worldwide Clinical Trials staff.
  • Basic knowledge of statistics and finance practices.
  • Strong leadership, management, and interpersonal skills.
  • Strong planning and organizational skills.
  • At least 7 years of clinical trial experience, including at least 4 years of experience in global clinical trials.
  • Hands-on experience in the day-to-day management of all aspects of global clinical trials.
  • Knowledge and appreciation of all stages of clinical drug development.
  • Strong knowledge of monitoring practices and demonstrated knowledge and competence in applying Code of Federal Regulations, Good Clinical Practice, and International Council for Harmonisation guidelines.
  • Effective leadership skills and a proven ability to build and foster high-performing team productivity and cohesiveness.
Responsibilities
  • Identify operational needs for upcoming projects and track and review current assignments for CAT Operations staff.
  • Resource CAT study projects as Resource Manager.
  • Serve as a subject matter expert for CAT Operations activities.
  • Provide operational oversight for designated CAT study projects.
  • Engage in and coordinate resourcing activities for all awarded CAT projects.
  • Identify training and skills gaps among staff and coordinate learning opportunities to enhance operations staff knowledge and skills in industry-related regulations, processes, materials, and guidelines.
  • Actively identify and engage in process improvement activities.
  • Participate in QMD reviews and new QMD development.
  • Author, collaborate on, and review QMD and guidance documents.
  • Coordinate and manage CAT Operations team meetings.
  • Provide active engagement and oversight of study risk assessments related to operational activities.
  • Work with department leaders to ensure alignment among CAT operational and clinical services.
  • Lead or contribute to departmental initiatives implementing policies, methods, and techniques that support existing service areas and department growth.
  • Oversee CAT study deliverables from launch through study closeout.
  • Assist and collaborate with Operations staff, Project Management, and Contracts on vendor and study budget development, scope-of-work revisions, tracking, and compliance.
  • Assist with vendor-management concerns, including escalations and Vendor Management and Quality Assurance meetings.
  • Review and assess ongoing budget utilization and revenue recognition with Operations Managers to ensure projects meet financial targets.
  • Manage internal CAT Operations meetings and other trial-specific meetings as appropriate.
  • Contribute significantly to strategic departmental, sponsor-related, and cross-functional initiatives.
  • Participate in business development activities, including proposal input, capabilities presentations, and bid defense meetings.
  • Apply thorough knowledge of industry regulations and guidelines to ensure operational compliance during clinical trial conduct.
Desired Qualifications
  • A master's degree, life sciences degree, MBA, or PMP certification.
  • At least 5 years of experience managing team members or project management experience.
  • Prior experience in psychiatry or central nervous system therapeutic areas.
Worldwide Clinical Trials

Worldwide Clinical Trials

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Worldwide Clinical Trials is a contract research organization that provides drug development services for pharmaceutical and biotech companies, focusing on running clinical trials to bring new medicines to market. Its core work centers on the science and logistics of clinical trials—designing studies, coordinating sites and investigators, and managing data and regulatory processes to advance drug candidates through development. The company differentiates itself through its specialized, science-driven approach and global expansion achieved via strategic acquisitions, building a larger network and broader capabilities to support complex trial programs. After a history of ownership changes, including a re-launch in 2007 and a majority stake sale in 2023, the firm aims to grow further under new ownership while continuing to offer focused clinical trial services that support medical advancement.

Company Size

1,001-5,000

Company Stage

Acquired

Total Funding

N/A

Headquarters

Morrisville, North Carolina

Founded

1986

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Simplify Jobs

Simplify's Take

What believers are saying

  • Catalyst closed by August 31, 2026, lifting employee count to about 4,400.
  • Medidata Plus expands AI workflow reach across study design, data, and patient experience.
  • Every Cure partnership and rare-disease events strengthen sponsor access and scientific credibility.

What critics are saying

  • Fortrea's September 2, 2026 deal strips out Worldwide's Austin and San Antonio early-phase engine.
  • Revelio shows 2026 headcount fell 1.5%, while job postings dropped 89.9% from 2025.
  • Catalyst integration through 2026 risks distraction, attrition, and duplicated oncology leadership layers.

What makes Worldwide Clinical Trials unique

  • Catalyst added oncology and FSP depth on January 20, 2026.
  • Worldwide became Medidata's first CRO to implement Medidata Plus on April 23, 2026.
  • Worldwide spans 70+ countries with neuroscience, oncology, rare disease, and internal medicine focus.

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Benefits

Remote Work Options

Growth & Insights and Company News

Headcount

6 month growth

5%

1 year growth

5%

2 year growth

0%
Clinical Trial Vanguard
Sep 3rd, 2026
Fortrea’s $45M Early-Phase Acquisition Will Reshape Your Phase I Startup Timeline, Are You Ready?

Fortrea's $45M acquisition of Worldwide Clinical Trials' early-phase division adds a 60,000 sq ft bioanalytical lab. Here's what it means for Phase I site…

GlobeNewswire
Sep 3rd, 2026
Fortrea acquires the clinical pharmacology unit and bioanalytical laboratory activities of Worldwide Clinical Trials.

Fortrea acquires the clinical pharmacology unit and bioanalytical laboratory activities of Worldwide Clinical Trials. This acquisition brings dedicated bioanalytical expertise and increased capacity to Fortrea's early clinical development network as Worldwide continues its strategy to strengthen its clinical development activities, therapeutic leadership, and presence in high-growth markets.

Australian Associated Press
Sep 2nd, 2026
Fortrea to acquire clinical pharmacology unit and bioanalytical laboratory operations from Worldwide Clinical Trials.

Fortrea to acquire clinical pharmacology unit and bioanalytical laboratory operations from Worldwide Clinical Trials. September 02, 2026 Adds dedicated bioanalytical capabilities and expanded capacity to Fortrea's early clinical development network as Worldwide advances its strategy to scale clinical development, therapeutic leadership and high-growth markets Highlights * Fortrea enters into a definitive agreement to acquire the Early Phase Services division of Worldwide Clinical Trials * Includes a 60,000 sq. ft. GLP bioanalytical lab in Austin; a 200-bed GCP-compliant clinical pharmacology unit in San Antonio; and a biospecimen storage facility in Pflugerville, Texas * Enables integrated execution of early-phase studies with large and small molecule bioanalytical capabilities, enhancing Fortrea's ability to deliver faster, more integrated early clinical development solutions for simple and complex clinical studies * Strengthens Fortrea's end-to-end clinical development platform, supporting customers from first-in-human studies through Phase IV and post-approval evidence generation * Supports Fortrea's growth strategy through expanded scientific capabilities, increased early clinical development capacity and enhanced ability to create long-term value for shareholders * Supports Worldwide Clinical Trials' existing rapid global growth across oncology, neuroscience, internal medicine, and rare disease

Citybiz
Jun 11th, 2026
WCG names Anthony Doyle chief financial officer to support growth.

WCG names Anthony Doyle chief financial officer to support growth. June 11, 2026 Anthony Doyle WCG has appointed Anthony Doyle as chief financial officer, effective June 15, 2026, adding a healthcare and clinical research finance executive as the company continues to expand its role in supporting clinical trial operations and decision-making. Doyle succeeds Robert VanHees, who will remain with WCG as a special advisor through Dec. 31, 2026, to support the transition. The leadership change comes as WCG seeks to strengthen financial operations, capital planning and organizational scale across its global clinical research platform. Doyle brings more than 20 years of financial leadership experience across healthcare, clinical research and both public and private equity-backed companies. He joins WCG from Flourish Research, a clinical trial site network, where he serves as chief financial officer. "Anthony brings a strong combination of financial rigor, operational leadership, and industry experience that aligns with WCG's strategic direction," said Sam Srivastava, chief executive officer of WCG. "He has a proven ability to scale finance organizations, lead complex capital strategies, and support high-growth businesses." Before joining Flourish Research, Doyle served as chief financial officer at BioCryst Pharmaceuticals and Worldwide Clinical Trials. In those roles, he led finance functions through periods of business expansion, operational transformation and capital strategy execution. Earlier in his career, he held finance leadership positions at General Electric, where he developed experience in operational finance, financial planning and analysis, and corporate development. His appointment comes as clinical research organizations and service providers face growing demand for technology-enabled solutions that can improve trial efficiency, reduce risk and support faster development timelines. As sponsors and research partners manage increasingly complex studies, companies such as WCG are expanding capabilities that combine regulatory oversight, data intelligence and operational support. WCG describes itself as a provider of clinical research decision infrastructure, helping organizations manage risk and make more confident decisions across the trial lifecycle. The company's work spans therapies at multiple stages of development, with a platform built around oversight, intelligence and data-driven support. Doyle said WCG's position in the clinical research ecosystem and its growth trajectory were key factors in his decision to join the company. "WCG plays a central role in advancing clinical research with a clear mission and a strong foundation for growth," Doyle said. "I'm excited to join the team and help drive disciplined execution, enable strategic investment, and support the company's continued momentum." Srivastava also credited VanHees for helping position the company for its next phase, noting his leadership and partnership over the past four years. The CFO transition reflects WCG's focus on scaling its financial and operational infrastructure as the company continues to serve pharmaceutical, biotechnology and clinical research partners. In a market increasingly shaped by data, artificial intelligence and pressure to improve trial performance, financial leadership is becoming central to how clinical research platforms invest, integrate capabilities and manage growth. With Doyle's appointment, WCG is adding an executive with experience across contract research, drug development and growth-stage healthcare organizations as it continues building its platform for clinical trial oversight and decision support.

Healthcare IT Today
Feb 2nd, 2026
Net Health Acquired Keet Health from WebPT | Worldwide Clinical Trials Enters Definitive Agreement to Acquire Catalyst Clinical Research

Net Health acquired Keet Health from WebPT | Worldwide Clinical Trials Enters Definitive Agreement to Acquire Catalyst Clinical Research. Check out today's featured companies who have recently completed an M&A deal, and be sure to check out the full list of past healthcare IT M&A. Net Health Advances Rehab Therapy Care with Acquisition of Keet Health from WebPT Net Health, a trusted provider of specialized software for rehab therapy and post-acute care, today announced the acquisition of Keet Health, a WebPT company, as part of a strategic collaboration with WebPT focused on advancing outcomes measurement and remote therapeutic monitoring (RTM) for rehabilitation therapy providers. Net Health's acquisition of Keet Health expands access to Net Health's Limber platform - the industry's leading solution for outcomes measurement, RTM, and digital home exercise programs. In connection with the transaction, Limber will become the preferred outcomes and RTM solution for WebPT and Clinicient customers, with an integrated experience targeted for early 2026. "Better outcomes are driven by better insights and stronger connections across the continuum of care," said Ron Books, CEO at Net Health. "Through our collaboration with WebPT, we're advancing outcomes measurement and remote monitoring in ways that help rehab providers extend care beyond the clinic, reduce fragmentation, and keep the focus where it belongs - on patients." Limber, which Net Health acquired in 2025, is a leading platform for outcomes measurement, RTM enablement, and home exercise delivery for rehab therapy providers. The solution delivers outcomes-informed insights that help clinicians monitor progress, personalize care, and support patients beyond traditional clinic visits. Net Health continues to invest in Limber's analytics and integration capabilities as part of its broader platform strategy to support value-based care. Net Health and WebPT also plan to invest in deeper integration between Limber and the WebPT and Clinicient platforms. The integration is intended to streamline workflows, strengthen data continuity, and support more connected digital health experiences as patients transition between care settings. "Our work with Net Health gives our members access to a powerful digital health solution while preserving the flexibility and choice they expect," said Andrea Facini, CEO at WebPT... Full release here, originally announced January 15th, 2026. Worldwide Clinical Trials Enters Definitive Agreement to Acquire Catalyst Clinical Research Worldwide Clinical Trials, a global contract research organization (CRO), has entered into a definitive agreement to acquire Catalyst Clinical Research, LLC, a specialized oncology CRO, known for its expertise in early phase oncology trials and a strong biometrics and Functional Service Provider (FSP) model. Following the close of the transaction, Nick Dyer, Chairman of the Board at Catalyst, will join Worldwide's Board of Directors, and Nik Morton, President and CEO at Catalyst, will join Worldwide's executive leadership team. This strategic combination creates immediate value for customers by establishing Worldwide as a leading oncology-focused CRO, while maintaining depth across multiple therapeutic areas and strengthening its footprint and scale to deliver larger global trials. The integration of Catalyst's two established solutions - Catalyst Oncology and Catalyst Flex - will strengthen Worldwide's portfolio, offering customers proven expertise and new services for full-service, FSP resourcing, and hybrid solutions. Additionally, the integration of complementary technology platforms and best-in-class operational practices will enable enhanced data visibility and improved efficiency throughout the development lifecycle - helping customers bring life-changing therapies to patients more quickly. "Bringing Worldwide and Catalyst together elevates our capabilities in oncology and provides a new solution for our collective customers," said Alistair Macdonald, Chief Executive Officer at Worldwide. "We are excited to add Catalyst's deep operational expertise and oncology credibility to our own well-known CNS specialist CRO capabilities to create a differentiated biotech-oriented oncology solution. Our combined customers seek focused senior executive connection and attention, predictability, speed, flexibility, and scientific rigor. They will benefit from the addition of a scalable FSP model with integrated onshore/offshore service lines, while we leverage advanced business management tools and AI to drive operational excellence. Beyond the science, this is about people - bringing together talented teams, expanding opportunities, and working together to deliver more agile trials for our customers." Matt Jennings, Executive Chairman at Worldwide and Senior Operating Partner at Kohlberg, the majority owner of the Company, commented, "Integrating Catalyst will accelerate Worldwide's growth in oncology and expand both its customer base and global reach simultaneously. Their specialized expertise, innovative platforms, and strong relationships with emerging biotech sponsors align perfectly with our vision for building a differentiated, technology-enabled CRO. This is a strategic step toward creating a more agile and competitive organization that can meet the evolving needs of clinical research globally." "This marks an exciting new chapter for both Catalyst and Worldwide. By joining forces, Catalyst brings our specialized early phase oncology expertise together with Worldwide's strength in late phase development, expanding our global footprint and delivering differentiated oncology solutions globally," said Nik Morton, President and Chief Executive Officer at Catalyst... Full release here, originally announced January 20th, 2026.