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SCRA - Senior Clinical Research Associate / JPM

Eingestellt von Progressive aus Düsseldorf

Projektbeschreibung

This is not your average SCRA/LCRA role as it does not require extensive monitoring of nationwide sites, but rather will require the individual to take on a diverse and hands-on role with the studies.

The candidate will be working on global studies and duties will include study set-up, vendor management, protocol development, eCRF development, and some international co-monitoring.

This individual will be pivotal to the success of the studies and you will laterally work with the project managers and directors to hit the key milestones of the project.

The role is for a seasoned professional with a solid number of years experience behind them.

This role will allow candidates to gain valuable experience that other vacancies do not provide - an ideal role for candidates looking to move up into the trial/project management roles but finding it tricky to get into that area, this will give you invaluable experience and facilitate that career move.

This is a company looking for people they can really invest in and you need to be an independent and motivated candidate with excellent people skills.

The contract is for an initial period of 6 months with a view to extend past the initial period or revert to permanent.

The role is office based in Cambridge for the first month, with a maximum flexibility of 2 days working from home for the rest of the contract.

Daily rate is market competitive and dependent on experience.

Key words:

CRA/ SCRA/ LCRA/ CRAI / CRAII/ clinical research associate / senior clinical research associate/ clinical monitor /clinical trials monitor / CRO/ clinical research organisation/ senior clinical research associate/ clinical monitor /clinical trials monitor / CRO/ clinical research organisation/ monitoring/ Clinical trials. Clinical Project Manager or Clinical Trial manager or Clinical study Manager or clinical studies manager or clinical programme manager or clinical programme director or CPM or CTM or Clinical Trial Head, CRO, Clinical research organisation, pharmaceutical, clinical trials, CRO, Clinical research organisation, pharmaceutical, pharma, clinical trials

To find out more about Progressive Recruitment please visit www.progressiverecruitment.com

Projektdetails

  • Vertragsart:

    Contract

  • Berufserfahrung:

    Keine Angabe

Geforderte Qualifikationen

  • Kategorie:

    Sonstiges

Progressive

  • Straße:

    Bleichstrasse 8-10

  • Ort:

    40211 Düsseldorf, Deutschland