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Safira Clinical Research Ltd is dedicated to advancing healthcare through high-quality clinical research. We work collaboratively to support studies that improve patient outcomes and contribute to medical innovation. Our team values accuracy, integrity, and a commitment to excellence in everything we do.
We are looking for a motivated and detail-oriented professional to join our team. This role offers the opportunity to contribute to meaningful clinical research activities while working alongside experienced professionals in a collaborative and supportive environment.
Support the planning, coordination, and delivery of eCOA activities
Maintain accurate study documentation and ensure records are complete and up to date
Work closely with internal teams, and external partners
Help ensure all eCOA activities are carried out in line with study protocols, regulatory requirements, and company procedures
Assist with data review, reporting, and administrative tasks related to ongoing research projects
Contribute to process improvements that support quality, efficiency, and compliance
Minimum of five years experience in eCOA Project Management at an eCOA Vendor or Sponsor
Strong organisational skills and close attention to detail
Excellent written and verbal communication skills
Ability to manage multiple priorities and work effectively to deadlines
A professional, collaborative, and proactive approach to work
Commitment to quality, accuracy, and ethical standards
The opportunity to contribute to research that supports better health outcomes
Exposure to a collaborative and purpose-driven clinical research environment
Ongoing learning and professional development opportunities
The chance to build your career within a growing and impactful organisation
At Safira Clinical Research Ltd, we value teamwork, professionalism, and continuous improvement. We are committed to creating an inclusive workplace where employees feel supported, respected, and empowered to do their best work.
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