Global Trial Manager, Late Phase Studies

🕒 July 15

🌐 Spain, United Kingdom, +1 more countries – Remote

🇪🇸 Spain – Remote 🇬🇧 United Kingdom – Remote 🇮🇪 Ireland – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

👔 Manager

👻 Ghost score 65%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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IQVIA

WebsiteLinkedInAll Job Openings

10,000+ employees

💼 Consulting

🏭 Manufacturing

📣 Marketing

💰 $1G Post-IPO Debt on 2023-05

Consulting • Manufacturing • Marketing

IQVIA is a global leader in data analytics and technology solutions, dedicated to improving health outcomes. The company utilizes its Connected Intelligence platform to harness the power of advanced data analytics and artificial intelligence, facilitating innovation in healthcare. IQVIA focuses on various areas, including clinical research, technology, and consulting services to solve complex healthcare challenges and accelerate the delivery of new therapies to patients.

📋 Description

• Lead critical aspects of global late-phase clinical studies as a core Clinical Trial Team member • Plan, coordinate and oversee assigned Medical Affairs activities from operational set-up through maintenance, reporting and closure • Act as the operational point of contact and build relationships with global stakeholders, investigators, external partners, reviewers, governance groups, CROs and vendors • Develop, coordinate, review and maintain study, program, submission and regulatory documentation • Coordinate Global Medical Affairs inputs for program-level and safety documents, including DSURs, PSURs, Investigator Brochures, Addenda to Clinical Overviews and annual regulatory reports • Organise and support kick-off, strategy, scientific review, governance and comment-resolution meetings • Maintain operational information, trackers, delegations, study or program status, metrics and reporting in systems and databases • Plan and monitor budgets and resources, including investigational product or Post-Study Drug Supply forecasts where relevant • Support selection, contracting and oversight of CROs and third-party vendors • Identify, assess and manage operational, quality, compliance, GCP and delivery risks and issues • Monitor adherence to SOPs, working practices, GCP and applicable requirements, maintaining audit and inspection readiness • Track assigned activities and outstanding items through final resolution • Contribute to process simplification, operational excellence, knowledge sharing and continuous improvement

🎯 Requirements

• Advanced degree in life sciences or healthcare • Minimum 5 years’ experience in planning, executing and reporting global clinical trials in a pharmaceutical company or CRO, preferably including at least 2 years managing Real World Evidence (RWE) or global late-phase studies (e.g. PASS, PAES, NIS), or relevant equivalent Medical Affairs experience (dependent on role pathway) • Experience working in global, cross-functional matrix teams and building effective relationships with internal and external stakeholders • Ability to manage multiple studies or programs of work in parallel, consistently delivering to time, budget and quality expectations • Strong planning, communication, influencing, problem-solving and organisational skills, with the ability to work independently and manage ambiguity and change • A quality and compliance mindset, high attention to detail and the confidence to speak up, challenge constructively and drive issues to resolution • Experience contributing to relevant clinical study documents (e.g. protocols, PSURs, DSURs, regulatory submissions) • Candidates must be based in Madrid, Spain; Reading, Berkshire, United Kingdom; or Dublin, Ireland • This role is not eligible for UK visa sponsorship

🏖️ Benefits

• Home-based work in Europe • Full-time employment