Clinical Research Lead

Pharmaceutical Research Associates, Inc; United Kingdom; On-site; GBP 50,000 - 90,000; Full time

Job summary

Join a leading clinical research organization as a Clinical Research Lead, where you will play a pivotal role in managing strategic clinical studies in the Oncology field. This position offers a unique opportunity to work closely with various stakeholders, ensuring the operational delivery of clinical trials while adhering to the highest standards of compliance and quality. You'll be part of a diverse and inclusive culture that values high performance and nurtures talent. With competitive benefits and a commitment to employee well-being, this role is perfect for those looking to make a significant impact in the clinical research landscape.

Benefits

Health Insurance

Retirement Planning

Employee Assistance Programme

Flexible Benefits

Annual Leave Entitlements

Qualifications

• 5+ years of clinical research experience in CRA or Project Management roles.
• Strong understanding of clinical trial methodology and GCP regulations.

Responsibilities

• Oversee local CRO activities and ensure project milestones are met.
• Collaborate with Clinical Study Teams to ensure high-quality deliverables.

Skills

Clinical Research Experience

Team Collaboration

Problem Solving

Effective Communication

Organizational Skills

Education

Bachelor's Degree in Life Sciences

Medical Background

Job description

Overview

Job title - Clinical Research Lead

Location - must be based in the UK

Sponsor dedicated

As a Clinical Research Lead you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Responsibilities

Working fully embedded within an ever expanding program that specializes in the Oncology space, you will be responsible for the operational delivery of strategic clinical studies assigned to the country, to support our client's pipeline, in accordance with ICH/GCP, our client's SOPs, local operating guidelines and local requirements, as applicable.

What you will be doing:

Support ADCO / DCO to:

• Oversee local CRO activities, acting as Single Point of Contact for key and strategic outsourced clinical studies, to ensure corporate and country objectives are reached and potential country issues properly followed-up.
• Collaborate and liaise with Clinical Study Teams and Global Monitoring, for in-house clinical studies conducted within country/ies ensuring key project milestones and high quality are delivered.
• Partner with local Study Startup Specialist (SSS) or Clinical Research Associates (CRAs) to ensure consistency and accuracy of all core documents for local EC submission, as applicable, for in-house clinical studies (i.e. submission pack, document customization, translations, quality check).

Support Feasibility process to:

• Act as the central point of contact for feasibilities in the country/ies, for both in-house and outsourced clinical studies when feasibilities are requested or deferred to country/ies by Global Teams
• Carry out top Level feasibilities, to collect key information on competitive clinical studies, marketed and non-marketed drugs, regulatory concerns, Standard of care, etc...
• Build up professional relationship with the investigators and Key Opinion Leaders.
• Liaise with Country, ADCO/DCA and EU CRA Manager for CRAs assignment
• Once trained, support the Global Monitoring team to conduct co-monitoring and CRA assessment visits, when needed and requested
• Supports ADCO / DCO to prepare internal initiatives, meetings and trainings (as required)
• Support the ADCO / DCO to implement local SOPs / WIs, quality/compliance review and initiatives, to ensure inspection readiness
• Act as a Site Relationship Partner for specific studies, to build and retain relationships through the lifecycle of the clinical study, to ensure an effective clinical study conduction and completion Act in accordance with company policies and procedures, SOPs, ICH/GCP guidelines, FDA regulations and local regulatory bodies.
• Collaborates with Medical Affairs Department, as well as all country internal stakeholders
• Collaborates and interact with QA, Global Monitoring, clinical Study Start-Up teams, Global Clinical Trial Managers (CTMs), Global Regulatory and other as work needs

Qualifications

You must have the following:

• At least 5 years clinical research experience as CRA or Lead CRA or Project Manager
• Bachelor or higher University degree in life sciences, nursing or medical background preferred
• Demonstrated knowledge of clinical trial methodology and drug development process, related to monitoring clinical trials, GCP, SOP and country-specific regulatory requirements.
• Demonstrated understanding of applicable medical/therapeutic area knowledge and medical terminology
• Demonstrated attitude to team work and cross-functional collaboration
• Ability to establish and maintain effective working relationships with co-workers, managers, internal and external stakeholders
• Effective oral, written and presentation skills, with the ability to communicate effectively with varied audiences
• Strong attitude to problem solving, effectively prioritize tasks and working independently
• Effective organizational and time management skills
• Available for domestic and international travel, including overnight stays up to approximately 20% of the working week

What ICON can offer you:

Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family's needs
• Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
• Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family's well-being
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others

Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits

At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.

https://careers.iconplc.com/reasonable-accommodations

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.