Senior Clinical Research Associate

€50000 - €55000 per annum
  1. Permanent
Munich, Bayern
  1. Clinical Operations, Monitoring
Posted: 06/03/2020
BBBH13614

This vacancy has now expired. Please see similar roles below...

Hobson Prior are seeking an experienced Senior Clinical Research Associate to join a global CRO that work on multiple specialist fields including, Gastroenterology, Infections Diseases and Hematology.

Job Responsibilities:

  • 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.
  • Delivering onsite training of investigators and staff; in-house project team training.
  • 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.

Key Skills:

  • Ability to work effectively in English and German
  • 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

Requirements:

  • University degree in Life Sciences, Pharmacy, MD or RN or an equivalent combination of education and experience
  • Experience at a similar position, with full scope of monitoring responsibilities within Phase II/III Clinical Trials
  • Participation in clinical projects in the capacity of a SrCRA and/or Lead Monitor
  • Knowledge of the local clinical research environment
  • Experience in regulatory submissions, contract negotiations, site management and feasibility assessment
  • Experience with oncology/haematology indications is preferable
  • Valid driver's license and ability to travel

Apply now:

If you are interested in learning more or applying to this exciting opportunity, please complete the form below and attach a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please request a call back at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.

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