Ref #: 28750

Employment type: Permanent - Full-Time

Location: Denmark - Copenhagen

Posted: 30-Apr-2021


In this role, you are the primary contact point between the sponsor and the investigational site, managing trials from start-up through data-base lock.

Your main responsibilities include (but not limited to);

- Site selection, site initiation visits, subject recruitment and retention, monitoring and close-out.

- Fully contribute to process improvement, training and mentoring of other CRAs.

- Ensures site staff have current GCP and necessary protocol and compound training to conduct the clinical trial.

- Contribute to site level recruitment strategy and contingency planning and implementation

-Regulatory assessment, drug supply management, etc

-Compliance with protocol, GCP, global and local regulations, global and local processes

This role requires;

- A Master degree in Life Sciences, Nursing, or related scientific field is required.

- A minimum of 2-5 years of clinical trial monitoring experience in oncology studies is beneficial

- Strong knowledge of ICH-GCP, company standard operating procedures, local laws and regulations, assigned protocols and associated protocol specific procedures including monitoring guidelines.

- Strong IT skills in appropriate software and company systems.

- Ability to work on multiple trials

If you are seeking the next step in your career, with a competitive salary and benefits package, together with long term development opportunities, please send your CV for review as soon as possible

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