Clinical Study Manager II- Fixed-term contract

7 maanden geleden

Groningen, Nederland PRA Voltijd

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.
With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.
Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

The Clinical Study Manager Role:


Provides clinical trial management for in-house and outsourced studies, performs quality checks, protocol and document
development, and executes study delivery plans aligned with program goals and timelines.

Based in Groningen, Netherlands.

Early Phase clinic.

Six month fixed-term contract

Responsibilities:

- Reviews and assesses the research protocol, clinic budget, case report forms, informed consent forms and study volunteer information. 
- Participates in the assessment, preparation and implementation of studies for the clinic to ensure a timely and high-quality study output.
- Conducts feasibility analysis. Reviews availability and workload for study volunteers, practicability and required personnel. Creates risk analysis and contingency plans. Coordinates in- and outpatient visits.
- Serves as liaison between all clinic groups and the applicable clinic management. Communicates any changes in scope and/or cost and escalates issues and/or major deviations. Serves as clinic contact for the study sponsor. 
- Prepares and reviews clinic documents.
- Ensures proper sampling, collection and transmission of research data samples. 
-Communicates any changes in scope and/or cost and escalates issues and/or major deviations. Serves as clinic contact for the study sponsor. 
- Monitors the study timelines and output by clinic staff according to protocol and internal procedures.

The individual employed into this temporary role will:

Learn the CSM role and the context of Early Phase Clinical Research

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.


Benefits of Working in ICON:


Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.

At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

ICON, including subsidiaries, is an equal opportunity and inclusive employer and is 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.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.

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