Job Description

Sr. Clinical Research Associate (United Kingdom)
Negotiable
Hybrid
Greater London, England, United Kingdom
PCD330193

About the organisation

At the organisation, our mission is to shine a light on new therapies that improve lives. When you join our team, you will use your unique skills, expertise, and knowledge to forge meaningful partnerships with clients while helping them turn groundbreaking ideas into life-changing treatments. If you are passionate about advancing pharmaceuticals and biologics, fueled by an entrepreneurial spirit, and eager to collaborate with top minds across science, business, and operations, we’d love to connect. Together we can accelerate innovation and grow side by side, making a last impact on patients worldwide. Together we SHINE.
Find more information about our values. the organisation! If you are interested in this role please apply through the button or for more information reach out to the recruitment team,
Disclaimers

Key Skills:
Minimum of 5 years’ experience as a CRA, preferably in oncology or rare disease.
Strong understanding of ICH-public cloud platform and regulatory guidelines.
Clear and confident communicator in English.
Ability to work independently and manage priorities.
Willingness to travel as required.
Salary (Rate): the organisation
City: Greater London
Country: United Kingdom
Working Arrangements: hybrid
IR35 Status: the organisation
Industry: Other
Bring your monitoring expertise to the forefront of innovation. We are looking for a Sr. Clinical Research Associate (Sr. CRA) to join our A-team (hybrid). As a Sr. CRA at the organisation, you will independently control and monitor investigational sites, pro-actively detect issues, provide solutions to ensure clinical studies are performed according to the trial protocol and in compliance with SOPs, applicable regulations, and the principles of Good Clinical Practice. At the organisationTM, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe. At the organisation we are big enough to deliver and small enough to care. We know all our colleagues by name and work together as a team to make everyone SHINE.
The role As a Sr. CRA, you will take the lead on monitoring activities, owning your sites and relationships with investigators. You will be the bridge between sponsor and site, ensuring trial integrity while being supported by a collaborative, experienced team. This includes work related to regulatory affairs, site activation processes-including contracting and start-up activities-to ensure smooth and compliant study execution. You will travel throughout The UK.

the organisation Responsibilities

Independently manage all aspects of monitoring for assigned clinical trials across study phases, including site initiation, routine monitoring, and close-out visits.
Ensure compliance with protocols, public cloud platform, ICH, SOPs, and applicable regulatory requirements.
Build strong site relationships, acting as a primary point of contact and ensuring high-quality data collection.
Identify and resolve site issues, escalating as needed to maintain trial integrity and patient safety.
Activities around regulatory affairs, site activation and study-startup.

Requirements

You are an experienced CRA ready to take the next step with a company that truly values your expertise and independence. You thrive in an agile, collaborative environment and want to be part of a team making a real impact. Experience leading monitoring activities in complex trials, ideally in oncology or rare disease with a minimum of at least 5 years’ experience. Strong understanding of ICH-public cloud platform and regulatory guidelines. Clear and confident communicator in English. Comfortable working independently and managing priorities. Willingness to travel, as required.

Key Responsibilities:

Independently manage all aspects of monitoring for assigned clinical trials across study phases, including site initiation, routine monitoring, and close-out visits.
Ensure compliance with protocols, public cloud platform, ICH, SOPs, and applicable regulatory requirements.
Build strong site relationships, acting as a primary point of contact and ensuring high-quality data collection.
Identify and resolve site issues, escalating as needed to maintain trial integrity and patient safety.
Activities around regulatory affairs, site activation and study-startup.

Benefits

Competitive salaries and a comprehensive benefits package
Departmental Study/Training for furthering professional development
Mentoring opportunities
Internal growth opportunities and career progression
Financially rewarding internal employee referral program
Eligibility for our internal employee recognition programs for going above and beyond on projects
Eligibility for our Loyalty Award Program in recognition of loyalty and commitment of longstanding employees