Study Coordinator 2

Panthera Biopartners; Greater London; On-site; GBP 27,000 - 33,000; Full time

Benefits offered by this job

25 days annual leave

Life insurance

Healthcare cash plan

Employee assistance programme

Annual Self Care Day

Cycle to Work Scheme

EV Scheme

Annual Leave Buy and Sell

Job summary

Panthera Biopartners in Enfield, England, invites applications for Patient Study Coordinator 2 to join our clinical research site. You will manage trial data, support regulatory compliance, and ensure study readiness through meticulous documentation and trackers.

This role requires strong organisation, precise data entry, and collaboration with study teams, monitors, and vendors. Prior experience in healthcare or CRO settings is desirable, and flexibility to work across Panthera sites may be

Qualifications

• Experience in data management within clinical trials or healthcare settings.
• Familiarity with ISF, logs, EDC and regulatory documentation.
• Able to work across busy site environments with attention to detail.

Responsibilities

• Oversee study trackers, timelines and enrolment progress.
• Lead day-to-day site management and Pre-Rand activities.
• Coordinate communication between study teams, monitors and site staff.
• Ensure accurate documentation, data entry and regulatory compliance.
• Support monitoring activities, CRA visits and safety reporting.

Skills

Data entry

Regulatory awareness

Organised

Query resolution

Job description

Study Coordinator 2 Panthera Biopartners Enfield, England, United Kingdom, EN3 4GS

Panthera Biopartners

Panthera is an independent Site Management Organisation helping pharmaceutical and contract research organisations find the right patient, for the right trial, at the right time. The Panthera team is run by a world-class team of experts with more than a hundred years of clinical research experience.

We put the patient at the heart of everything we do to ensure the best experience and environment for volunteers and participants. Accelerating clinical breakthrough for our customers, our patients, and for future generations.

An exciting opportunity has arisen for a Patient Study Coordinator 2 to join our team at our Enfield Clinical Research Site!

Salary & Benefits Package

• Salary starting from; £30,030
• 25 days annual leave plus bank holidays increasing with length of service
• Annual Leave Buy and Sell Scheme
• Life insurance - 3x annual salary
• Employee healthcare cash plan
• Employee Assistant Programme
• Enhanced sickness and family friendly policies
• Annual Self Care Day
• Cycle to Work Scheme
• EV Scheme

Job Summary

The Patient Study Coordinator 2 plays a key role in managing clinical trial data and supporting site compliance with regulatory and protocol standards. The role involves detailed data entry, documentation tracking, CRA visit preparation, and ensuring clinical and administrative readiness across all trial activities.

There may be a requirement to work across local Panthera sites as required from time to time.

Key Responsibilities

• Oversee study trackers, timelines, enrolment, and overall study progress
• Lead day-to-day site management and ensure study readiness (including Pre-Rand activities)
• Coordinate communication between study teams, vendors, monitors, and site staff
• Ensure accurate documentation, data entry, and regulatory compliance (ISF, logs, EDC)
• Support monitoring activities, CRA visits, and safety reporting (including SAEs)

Ideal Candidate

• Highly organised and data driven.
• Skilled in accurate, timely data entry and query resolution
• Evidence of experience working in a similar environment.
• Previous experience in the healthcare sector is desirable but not essential.

Panthera Biopartners provided the following inclusive hiring information:

We are an equal opportunity employer and consider all qualified applicants equally without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, veteran status or disability status.

PI3f37885987dc-30511-41414682

Full-time