Senior CDC/CDC II

Senior CDC/CDC II _ Office Based ICON is a global healthcare intelligence and
clinical research organisation united by a mission to bring new medicines and
treatments to patients faster. As a values-driven organisation, integrity,
collaboration, agility, and inclusion are at the heart of how we work and
interact with each other, customers, patients and suppliers. We are currently
seeking a Senior Clinical Data Coordinator to join our diverse and dynamic team.
As a Clinical Data Coordinator at ICON, you will play a pivotal role in
designing and analyzing clinical trials, interpreting complex medical data, and
contributing to the advancement of inNvative treatments and therapies. What you
will be doing Create and maintain detailed data management plans and
documentation, ensuring compliance with industry standards and regulatory
requirements. Participate in the identification and resolution of data
discrepancies and issues, working to streamline data flow and enhance data
quality throughout the study lifecycle. Collaborate closely with
cross-functional teams, including clinical operations and biostatistics, to
develop and execute data management strategies tailored to specific studies.
Perform other project activities as required in order to ensure that study
timelines are met (for example, filing and archiving of study documentation ,
dispatching of queries to investigator sites for resolution, etc.). Mentor
junior data coordinators, providing expert guidance on data reconciliation,
coding, and cleaning procedures. Your profile Bachelor's degree in a relevant
field, such as Life Sciences or Healthcare. Proven experience in clinical data
management within the pharmaceutical or biotechNlogy industry. Familiarity with
data management software and systems (e.g., Medidata, Oracle RDC, or similar).
Strong attention to detail and the ability to work effectively in a fast-paced
environment. Excellent communication skills and the ability to collaborate with
cross-functional teams. KNwledge of regulatory guidelines and standards (e.g.,
ICH-GCP) is a plus. Employment with ICON is contingent upon having the legal
right to work in the country where the role is based. Rewards & Benefits ICON
offers a competitive and comprehensive total rewards package designed to support
your health, wellbeing, and career development. Benefits may include:
Competitive base salary and performance related incentives Health and wellbeing
programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans Life assurance and disability coverage Employee
assistance programmes and wellbeing resources Learning and development
opportunities through structured training and career pathways Benefits may vary
depending on role and location. Visit our careers site to read more about the
benefits ICON offers. Inclusion and Accessibility ICON is an equal opportunity
employer. We are committed to building an inclusive and accessible workplace
where everyone feels valued and supported. If you require reasonable
accommodations during the recruitment process, please let us know or submit a
request here. Are you a current ICON Employee? Please click here to apply ICON
is an award-winning workplace that enables you to make a difference to patients’
lives by being part of a world-class clinical research organisation that helps
deliver new medicines & medical devices that are benefitting patients worldwide.
You are also part of a diverse company that cares about our world and is
dedicated to conducting business more sustainably and supporting the communities
in which we live. If you’re as driven as we are, join us. You’ll be working in a
great environment, with some of the brightest and the friendliest people in the
sector, and you’ll be helping shape an industry. Didn’t find the role you were
looking for? Even if the perfect role isn’t available right now, we’re always
excited to connect with talented individuals. Register to our Talent Community
to receive updates on roles that align with your career goals.