Clinical Research Associate III

Novotech; London; On-site; GBP 30,000 - 50,000; Full time

Job summary

Novotech is on the lookout for a Clinical Research Associate in London to manage clinical site oversight and regulatory compliance. Ideal candidates will possess 2-3 years of experience in monitoring, be proactive in problem-solving, and able to thrive in a collaborative project environment. The role includes a diverse range of responsibilities, providing a dynamic and rewarding opportunity to contribute to meaningful clinical research.

Benefits

Flexible working options

Paid parental leave for both parents

Wellness programs

Ongoing development programs

Qualifications

• 2-3 years of monitoring experience required.
• Excellent knowledge of ICH/GCP and local guidelines.
• Fluency in written and verbal English essential.

Responsibilities

• Managing investigator recruitment and regulatory submissions.
• Monitoring clinical sites and maintaining study files.
• Serving as primary site contact for compliance issues.

Skills

Monitoring experience

Knowledge of clinical trial process

Organizational skills

Time management

Coaching and mentoring

Fluency in English

Job description

Job Description

As a Clinical Research Associate, you will be expected to actively participate in and manage the recruitment of potential investigators and perform CA and EC submissions. You will be responsible for monitoring clinical sites, maintaining study files, conducting pre-study and initiation visits, liaising with vendors, and other duties. You will serve as the primary contact for sites regarding regulatory compliance and protocol questions, communicating with clinical sites to address and resolve issues. Reporting to the Clinical Operations Manager, you will be a key member of the Clinical Operations team in the United Kingdom.

We are searching for an ambitious and energetic person, capable of undertaking challenges in the project, pushing forward development, and functioning well within the project team. The ideal candidate should be open to cross-cultural communication and cooperation, and be significantly independent in their performance.

Minimum Qualifications & Experience:

• At least 2-3 years of monitoring experience
• Excellent knowledge of the clinical trial process, ICH/GCP, and local requirements/guidelines
• Excellent organizational and time management skills
• Ability to handle multiple priorities, work with deadlines, and perform under pressure
• Skills to coach and mentor other clinical staff
• Fluent in written and verbal English

Job Responsibilities:

• Recruitment of potential investigators, involvement in CA and EC submissions, and notifications to regulatory authorities.
• Translation of study-related documentation, organization of meetings, and other tasks as instructed by the supervisor.
• Monitoring of clinical sites, maintenance of study files, conducting pre-study initiation visits, regular visits, and close-out visits.
• Assisting on audit/inspection visits, site and vendor contracting processes, liaising with vendors, and other duties.
• Serving as the primary contact for sites regarding regulatory compliance and protocol questions, communicating ongoing issues.
• Supporting Business Development activities.
• Potential supervisory functions in clinical projects.
• Training, coaching, and supervising junior staff may be required.

Novotech is proud to offer a great workplace, committed to gender equality and providing an inclusive environment where everyone is treated fairly and with respect.

Our team members are passionate about our work, but we understand work is only one aspect of their lives. We support flexible working options, paid parental leave for both parents, flexible leave entitlements, wellness programs, and ongoing development programs.

We welcome applicants who are passionate about clinical research and biotech, including those who identify as LGBTIQ+, have a disability, or have caring responsibilities.

We are a Circle Back Initiative Employer and commit to responding to every application. We look forward to contacting you regarding your application.

About Us

Novotech is a global full-service clinical Contract Research Organization (CRO).

Headquartered in Sydney, Australia, with 34 offices across Asia-Pacific, North America, and Europe, employing over 3000 staff and partnering with over 5000 sites, we have the resources and infrastructure to scale regionally and globally as clinical programs advance.

We provide services across all clinical trial phases and therapeutic areas, including feasibility assessments, regulatory submissions, data management, statistical analysis, medical monitoring, safety solutions, central lab services, report writing, and vendor management. Novotech holds ISO 27001 and ISO 9001 certifications, ensuring high standards in information security and quality.

About the Team

Our team has advanced therapeutic and regulatory expertise, capable of executing across markets with a client-centric service model, providing our clients with trusted, long-term partnerships and accelerated pathways to market. Employees have the opportunity to develop their careers within a diverse, supportive, and collaborative global organization, working with clients at the forefront of life sciences.

At Novotech, you will work alongside empowered teams committed to success, fostering a culture of partnership and collaboration, where every voice is valued, with ongoing support from senior stakeholders and leadership.