Research Operations Specialist
4 dagen geleden
About ICON plc
ICON plc is a world-leading healthcare intelligence and clinical research organisation.
We advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.
Our patients are at the centre of all that we do, helping to accelerate the development of drugs and devices that save lives and improve quality of life.
We have a mission to succeed and a passion that ensures what we do, we do well.
The Role:
This fixed-term contract is for a Clinical Study Manager II.
You will be based in Groningen, Netherlands and work in our Early Phase clinic.
The role is six months long.
As a Clinical Study Manager II, your key responsibilities will include:
- Study Management: You will review and assess the research protocol, clinic budget, case report forms, informed consent forms and study volunteer information.
- Study Implementation: You will participate in the assessment, preparation and implementation of studies for the clinic to ensure a timely and high-quality study output.
- Feasibility Analysis: You will conduct feasibility analysis, reviewing availability and workload for study volunteers, practicability and required personnel. Create risk analysis and contingency plans, coordinate in- and outpatient visits.
- Liaison: You will serve as liaison between all clinic groups and the applicable clinic management, communicating any changes in scope and/or cost and escalating issues and/or major deviations.
- Sponsor Communication: You will serve as clinic contact for the study sponsor, ensuring proper sampling, collection and transmission of research data samples.
- Timelines and Output Monitoring: You will monitor the study timelines and output by clinic staff according to protocol and internal procedures.
About the Opportunity:
This role offers you the chance to learn the CSM role and the context of Early Phase Clinical Research.
You will have the opportunity to assist the CSM team with all of the above role responsibilities cross a broad range of study and population types including patient research.
Why Join Us?
We offer a comprehensive and competitive total reward package that comprises an excellent level of base pay, variable pay and recognition programs.
We also provide best in class employee benefits, supportive policies and wellbeing initiatives tailored to support you and your family at all stages of your career.
At ICON, we are an equal opportunity and inclusive employer, committed to providing a workplace free of discrimination and harassment.
All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
Estimated Salary:
The estimated salary for this role is around €60,000 per annum, depending on experience.
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