Clinical Study Start Up Specialist

Randstad UK; Welwyn Garden City; Vor Ort; GBP 90.000 - 130.000; Vollzeit

Zusammenfassung

Roche in Welwyn Garden City is seeking a Senior Start-Up Lead to drive efficient study activation for Roche-sponsored trials. You will collaborate with country teams, CROs, and global study groups to ensure timely initiation and regulatory readiness across diverse therapeutic areas.

The role emphasizes UK-specific start-up processes, responsible for regulatory submissions (HRA, Ethics, MHRA) and ongoing amendments, vendor relationships, and cross-functional planning to deliver trial milestones

Qualifikationen

• Degree in life sciences or equivalent required.
• Experience in clinical trial start-up and regulatory submissions.
• Strong understanding of UK regulatory environments and start-up systems.
• Excellent communication and organizational skills.

Aufgaben

• Lead country strategy for trial start-up and liaise with CROs and internal teams.
• Oversee start-up operations to ensure site activation and regulatory compliance.
• Coordinate with global teams to align with timelines and policies.
• Manage amendments throughout the study lifecycle.
• Engage with ethics boards and health authorities on trial policies.

Kenntnisse

Clinical trial start-up

Regulatory submissions

Cross-functional collaboration

English fluency

Problem-solving

Ausbildung

Life sciences degree

Postgraduate degree desirable

Tools

IRAS

CPMS

iCT

ARSAC

Veeva Vault

CTIS

RIM

Jobbeschreibung

Purpose, Objectives and Scope of Position

As a member of the PDG Country Study Start-Up Team, your primary focus is to drive and facilitate efficient study start-up processes to contribute to the delivery of clinical trials to patients. You will enable innovative clinical trial delivery, address study start up needs across various therapeutic areas, and ensure seamless trial execution for patients, investigators, and clinical site staff. Collaboration with local internal and external country teams, global study teams, and CROs is essential to this role.

Key Responsibilities

This role focuses on the efficient and compliant initiation of Roche-sponsored clinical trials by developing and implementing effective start-up strategies, overseeing start-up operations, and driving process improvements at the country and site level while maintaining regulatory compliance.

Key responsibilities include:

• Leading the country strategy for study start-up, driving efficiency, innovation, and collaboration with external stakeholders.
• Overseeing start-up operations and ensuring timely and efficient site activation and regulatory compliance.
• Ensuring alignment with global strategies and timelines.
• Managing amendments throughout the study lifecycle.
• Engaging with government and institutional bodies to align on clinical trial policies and practices (e.g., with Ethics Boards, Health Authorities).

You will lead in a cross functional environment in multiple of the following areas below:

• Lead teams in the creation of the study start-up strategy and execution of the study start-up process, encompassing strategy development, proactive risk mitigation, regulatory compliance, stakeholder liaison, tracking, knowledge management, and collaborative planning with CRO partners.
• Architect and strategically oversee ICF management, including preparation, submission, archiving to ensure compliance, alignment with the corporate requirements and best practices

Clinical Trial Submissions & Regulatory Coordination:

• Lead the development and oversight for UK clinical trial submissions (HRA, Ethics and MHRA), amendments and regulatory coordination, managing packages, responding to queries, ensuring document maintenance, and supporting amendments throughout the trial lifecycle.

Site Documentation & Compliance:

• Strategically manage site documentation and compliance, overseeing document collection/validation, coordination of related processes, and local vendor management (excluding CROs) if needed.
• Oversee the preparation and translation of patient-facing materials, as required
• Maintain up-to-date knowledge of country-specific regulations, including those for medicinal products, medical devices, and IVDRs

Site contracting and payment Management:

• Provide comprehensive strategic planning, oversight and implementation for all aspects of budgeting and contract management, including drafting clinical site budgets using the interactive costing tool (iCT), negotiating and implementing contracts, confidentiality disclosure agreements, indemnity/insurance documentation, and amendments, ensuring financial and legal alignment through collaboration with internal and external stakeholders, and maintaining accurate contract data in systems to support effective planning and forecasting
• Strategically oversee the payment processes, escalations, and reporting, ensuring financial/regulatory contract compliance and participating in planning, management, and reconciliation of financial activities.

Qualifications

• Degree (MD, PhD, MA/MS, BA/BS) in life sciences or equivalent. Postgraduate degree or master’s degree highly desirable
• Demonstrated experience in clinical trial start-up, regulatory submissions, and cross-functional collaboration
• Strong experience with UK specific clinical start up systems including IRAS, CPMS & iCT and ARSAC
• Strong understanding of ICH-GCP, EU CTR, and local regulatory environments
• Experience managing vendor/CRO relationships
• Experience management site relationships and leading leading site set up through to site activation
• Excellent communication and interpersonal skills
• Strong organisational, analytical, and problem-solving capabilities
• Proficiency in clinical systems (Veeva Vault, CTIS, RIM, etc.)
• Collaborative and adaptable mindset with attention to detail
• Ability to lead through complexity and ambiguity, especially in matrixed and global teams
• Fluency in written and spoken English is mandatory.
• Fluency in written and spoken language(s) of the host country is mandatory.