Urgent Need for a Senior Clinical Trial Associate with Investigator Sponsored Studies experience - Homebased in the UK
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.
Urgent need for a Senior Clinical Trial Associate to join our team beginning of August! The role is homebased in the UK.
This is a great career opportunity for a Senior CTA with solid clinical trial coordination experience to support investigator-led studies activities! You will bring relevant skills and experience to take on Manager’s tasks as required and will need to show initiative, ability to 'lead' and take action as needed.
You will be working to support the Managers in the implementation of investigator sponsored studies and support unsolicited investigator sponsored studies requests to advance science and clinical medicine.
Your responsibilities:
working with other members to support the timely execution and completion of deliverables in accordance with standard operating procedures (SOPs) and other supporting documentation
entering data into source systems, tracking essential documents and filing them to the central document repository
supporting execution of operational metrics
coordination and preparation for meetings (e.g., drafting agendas/minutes, scheduling speakers, materials collation)
providing support for numerous other aspects of the process (e.g., compiling documents for review submission, budget and contract generation, site initiation packet review and approval, and study close-out), this could also include creating and monitoring purchase orders, ad hoc administrative projects, and assisting with formatting of presentations.
Preferred Qualifications
BA/BS/BSc in the sciences or RN
Ideally a minimum of 5 years’ work experience in life sciences or medically related field
Previous experience with Investigator Sponsored Studies would be a real advantage
Clinical trial administration and coordination gained ideally within biopharmaceutical company, clinical research industry or clinical operations experience (experience obtained working on investigator-sponsored, industry-sponsored or industry partnered clinical trials, or working on clinical trials at a biotech, pharmaceutical company or CRO)
Key Competencies
- Attention to detail and organized with ability to multi-task and prioritize
- Written and oral communication; ability to work independently and in a team
- Delivery focus; reliable and respond promptly to requests
- Relationship building
- Policy, process and procedural conformance
- Problem solving, exercise initiative
- Flexibility
- Strong MS Office Excel would be preferred
What is offered
- A full-time and permanent contract of employment with us seconded to one single sponsor
- Home-based
- Salary according to level of skills and experience
- Company benefits: 23 days annual leave plus UK Bank Holidays, pension and healthcare
#LI-ET1
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.
