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• Highly competitive compensation
• Attractive benefits (Healthcare, Pension, Security, Annual bonus incentive, excellent support and well-being packages)
• Engaging employee programs
• In-depth company/role specific onboarding programs
• Remote & flexible working

• Database setup.
• Study documentation development.
• Equipment distribution/tracking.
• Report creation/distribution.
• Archival of study documentation.
• Coordinating Project Assurance meetings and assisting with compiling meeting minutes and action items.
• Facilitating issue management by documenting and tracking progress and ensuring timely resolution to customer escalations.
• Responding to customer inquiries and participating in customer calls/meeting upon Project Manager’s request.
• Taking the lead in managing various aspects of a project as requested.
• Supporting financial components of study management including: Assistance with documentation/database updates due to scope changes, Follow-ups related to invoice reconciliations, Preparation of reports in support of study forecasting activities.
• Ensuring compliance with timely training completion
• Other related projects and tasks as assigned.

• BSc, MSc, PhD in a relevant subject related to the Pharmaceutical / Healthcare / Life Science industry
• Demonstrable experience within a Pharmaceutical company, Biotech or CRO as a “Project Assistant” / “Project Coordinator“ is essential
• Previous experience working with eCOA, IRT/RTSM, eConsent, ePRO or other eClinical / Clinical technology solutions is highly advantageous to applicants
• A background in Clinical Research as a Clinical Research Associate or Clinical Research Manager is highly advantageous to applicants
• Ability to understand and interpret clinical trial documentation such as protocols, questionnaires and other data collection instruments.
• Experience using Planview or similar Project Management systems
• Excellent organizational, interpersonal, time management, and prioritization skills
• Excellent verbal and written communication skills
• Working knowledge of Microsoft Office products
• Self -directed - comfortable working in a dynamic & evolving environment

Courageously Curious

Our appetite to blend the best of domain expertise, technology and human understanding knows no bounds. We’re relentless in pursuing the information, insights and inspiration that means we can continuously improve clinical trial site support services and technology solutions.

Behaviors:

• We learn; embracing change, questioning how we work, finding a better way. And if it doesn't go to plan, we don't blame each other; instead, we own it and grow together
• We partner' with each other, with customers, patients and sites, working with them to understand their goals and then deliver the best solutions, Deliver Exceptional

We step forward because responsibility powers us; we don’t leave others to do what we can do ourselves. We take charge of events, delivering exceptional work for our customers, patients and each other.

Behaviors:

• We prioritize; focusing on what matters, never compromising on quality.
• We commit; delivering what we say we will, working with energy and intent, sharing what we learn with each other., People first, always

We think of others before we think of ourselves. We have a deep understanding of our customers, and deep empathy for patients—and each other. We’re united by our purpose—it’s why we go above and beyond to support each other, emphatically.

Behaviors:

• We do the right thing; for our customers, patients, sites and each other. And We're passionate about it.
• We lift each other up; respectful of different views, we listen are inclusive, and support each other to succeed.