Clinical Research Associate (II & Senior)

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Upsilon Global are currently cooperating with a rapidly expanding global mid-size CRO to find Dutch-speaking Clinical Research Associates (II & Senior) in Belgium/Netherlands to join their rapidly growing operations.

Our partner works with innovative biotechs and sponsors on complex clinical trials at the cutting edge of the industry in rare diseases, regenerative medicine, gene therapy, immunology, and more. This is a great chance for you to expand your personal portfolio and bolster your CV, working on the newest innovations.

They take pride in having the highest quality standards in the industry, giving you a fantastic opportunity to improve the health and lives of patients across the world. They have been subsequently recognised as the #1 CRO in the world for operational excellence at the 2021 CRO Leadership Awards, alongside winning in the five core categories.

They offer you extensive high quality training, providing stability with excellent opportunities for career development and speedy promotion. Their staff turnover rate is only 5% when compared to the industry average of 25%, which truly represents their ability to provide respect and recognition to you as an employee.

Office-based (Geel) or Home-based - Salary up to €80K & benefits (experience dependent)

The scope of responsibilities will include:

• Preparation, conduct, and reporting of selection, initiation, routine and closeout monitoring visits
• Site management, general administration of clinical research studies
• Supervision of study set-up, clinical monitoring and site management activities on a country level
• Monitoring trial progress and ensuring that project timelines and patient enrolment schedules are met
• Facilitating site contractual start-up and site budget processes
• Coordination of site regulatory documents collection
• Management of investigator site payments
• Communication point for investigational sites, project teams and support staff
• Back up communication point for vendors and clients
• Delivering onsite training of investigators and staff; in-house project team training
• Preparation and delivering of presentations at Investigator’s Meetings
• Compliance monitoring, participation in quality control activities; review of monitoring reports
• Preparation for and attendance at company’s audits; follow up and resolution of audit findings
• Maintenance of study-specific and corporate tracking systems at site and country level
• Participation in feasibility research

Desired Skills and Experience:

• University degree in Life Sciences, Pharmacy, MD or an equivalent combination of education and experience
• Experience at a similar position, with full scope of monitoring responsibilities within Phase I/II Clinical Trials
• Participation in clinical projects in the capacity of a CRA
• Knowledge of the local clinical research environment
• Experience with oncology, haematology, infectious diseases, GI indications is preferable
• Ability to work effectively in English and Dutch
• Team oriented with good communication and interpersonal skills
• Ability to multitask and work proactively in a fast-paced environment
• Good problem solving abilities, flexibility, organisational skills
• Valid driver’s license and ability to travel