Site Engagement & Feasibility Specialist

Life Sciences WA; Greater London; On-site; GBP 40,000 - 60,000; Full time

Benefits offered by this job

Flexible working options

Paid parental leave

Wellness programs

Ongoing development programs

Job summary

A leading clinical research organization in Greater London seeks a Site Engagement & Feasibility Specialist to optimize site strategies and conduct feasibility assessments. This role involves collaboration with project managers and clinical teams, requiring strong critical thinking and communication skills. Candidates should possess a degree in clinical or life sciences and have at least 1–2 years of relevant experience. The position offers a supportive work environment with flexible options and a commitment to inclusivity.

Qualifications

• Minimum 1–2 years’ experience in feasibility or site management within a CRO or pharmaceutical company.
• Previous experience in feasibility and/or study start-up is highly regarded.
• Strong communication skills with ability to prioritise tasks and meet deadlines.

Responsibilities

• Collaborate with managers and clinical teams to support feasibility activities.
• Act as a key liaison between the clinical team and stakeholders.
• Maintain relationships with key opinion leaders and investigators.
• Conduct literature reviews to support strategy development.
• Design feasibility questionnaires using CTMS Feasibility module.
• Support site engagement visits with Country Managers and Feasibility leadership.
• Analyse feasibility responses with proactive follow-up and strategic thinking.
• Provide regular updates to internal teams and clients and contribute to proposal documentation.

Skills

Strong communication skills

Critical thinking

Attention to detail

Ability to prioritize tasks

Education

Degree in clinical or life sciences

Job description

Site Engagement & Feasibility Specialist

United Kingdom

Job Description

Brief Position Description:

The Site Engagement & Feasibility Specialist (SEFS) is a key member of the Regulatory Operations team, responsible for ensuring Novotech delivers optimal site strategies to clients for each new business opportunity. SEFSs also collaborate with Project Managers to conduct post-award feasibility assessments, refining site selection.

Working closely with the Therapeutic Strategy Manager/Director (pre-award), Project Manager (post-award), and the Clinical Team, including the Site Engagement and Feasibility Manager and Feasibility Coordinator, the SEFS acts as the Regional Feasibility Lead for all feasibility activities for assigned projects. This includes direct engagement with Country Managers and local clinical teams.

Success in this role requires strong critical thinking, attention to detail, and the ability to work within tight timelines.

Minimum Qualifications & Experience:

A degree in clinical or life sciences. Relevant qualifications in allied health professions may also be considered.

Previous experience in feasibility and/or study start-up is highly regarded.

Strong communication skills, with the ability to prioritize tasks and meet deadlines.

Site Engagement & Feasibility Specialist: Minimum 1–2 years’ experience in feasibility or site management within a CRO or pharmaceutical company.

Responsibilities

• Collaborate with the Therapeutic Strategy Manager/Director (pre-award), Project Manager (post-award), and Clinical Feasibility Team to support feasibility activities.
• Act as a key liaison between the Clinical Team and other internal stakeholders to ensure seamless communication and project execution.
• Build and maintain strong relationships with key opinion leaders, investigators, and site staff across multiple therapeutic areas.
• Conduct literature reviews and utilisation of commercial databases and internal tools to support feasibility strategy development.
• Design study‑specific feasibility questionnaires using the CTMS Feasibility module.
• Collaborate with Country Managers, Directors, and Site Engagement and Feasibility Manager to support site engagement visits.
• Analyse feasibility responses critically, demonstrating proactive follow‑up and strategic thinking to optimise results.
• Use reporting tools to provide regular updates to internal teams and clients; contribute to proposal documentation as needed.
• Present feasibility findings to clients via teleconferences, in‑person meetings, and bid defences.
• Prepare comprehensive feasibility reports for post‑award (paid) assessments.
• Manage the preparation and collection of Confidential Disclosure Agreements.

Represent Novotech at external events (e.g., KOL engagement visits, site meetings, vendor meetings, professional association). Be mindful of the role of ambassador for Novotech when conducting day to day business.

Understand the responsibilities of Novotech as a service provider in the pharmaceutical and biotech industry and ensure all communications with external parties present a positive professional image of the company.

Benefits & EEO

Novotech is proud to offer a great workplace. We are committed to being an employer of choice for gender equality and providing an inclusive work environment where everyone is treated fairly and with respect. Our team members are passionate about what we do, but we understand work is only of the things that is important to them. We support our team members with flexible working options, paid parental leave for both parents, flexible leave entitlements, wellness programs and ongoing development programs.

We are looking for people who are passionate about working clinical research and biotech, including people who identify as LGBTIQ+, have a disability or have caring responsibilities.

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