Site Manager - EMEA

Posted 01 July 2021
salarisNegotiable
LocatieMokum, Amsterdam, Noord-Holland
Job type Permanent
BedrijfssectorenScience
referenceBBBH463850_1625155294

Job description

For our client, a key player in the pharmaceutical business, we are looking for a Site Manager EMEA who will provide Trial Co-ordination and Site Management services as primary point of contact between the sponsor and the investigational site.

Location: EMEA remotely

Responsibilities

  • Ensuring trial sites are inspection ready through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), International Conference on Harmonization for Good Clinical Practice (ICH-GCP), applicable regulations from start-up through data-base lock. Further, services will include pre-trial assessment, site selection, subject recruitment and retention planning, site initiation, monitoring and close-out.
  • Partners with the Clinical Trial Assistant (CTA)/Investigator Document Assistant (IDA), Local Trial Manager (LTM) and Central Trial Manager (CTM)/Global Trial Manager (GTM) to ensure overall site management while performing trial related activities for assigned protocols.
  • Contribute to quality Site Selection through participation in site feasibility and/or pre-trial site assessment visits, providing recommendation from local area about site/investigator selection in collaboration with the trial team, as required.
  • Act as primary company contact for assigned trial sites, engaging with Investigator and Site Staff throughout the life of the trial (investigator meetings, site visits, quality communication, etc.).
  • Drive study compliance by executing activities within site initiation and start-up, site monitoring, site management and site/study close-out according to internal SOPs/WIs/IFUs and policies. Ensures site staff is trained and the corresponding training records are complete and accurate at any time during all trial phases.
  • Contribute to site level recruitment strategy and contingency planning and implementation in partnership with other functional areas to achieve clinical research target.
  • Ensures site is equipped to carry out the trial with adequate site study supplies (such as Non-IP, lab kits, etc.) and clinical drug supplies.
  • Ensures trial subject safety in that all AEs/SAEs/PQCs are reported within the required reporting timelines and documented as appropriate, with supporting data collected and verifiable with information in the source documents.
  • Ensures Inspection readiness for sites by maintaining complete, accurate and timely data and essential documents in systems utilized for trial management (e.g. CTMS and eTMF/IF) according to expectations (metrics) and archiving retention requirements, including storage in a secure area at all times.
  • Focuses on Investigator engagement through timely follow up with sites.
  • Collaborates with LTM for documenting and communicating site/study progress and issues to trial central team.
  • Works closely with LTM to ensure CAPA is completed for QA site audits and for quality issues identified at the site during routine monitoring and other visit types, e.g. On Site Quality Monitoring Visit (OSQMV).
  • If applicable, will support negotiation of investigator budgets at site level, support tracking of costs and ensure payments are made at site level, maintaining site relationships.

Requirements

  • BA/BS degree/Degree in a health or science related field or equivalent industry experience
  • 3 to 5+ years of clinical trial monitoring experience or equivalent industry experience and completion of a monitoring training course
  • Specific therapeutic area experience depending on the services need.
  • Strong working 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.
  • Willingness to travel with overnight stay away from home according to business needs.
  • Proficient in speaking and writing in English and the country language where services will be provided (either France, Nederlands, Belgium, Spain, Israel). Effective communication skills, oral and written.
  • Experience with monitoring and site management of complex Early Phase of clinical development, as applicable.




Rabea Osterloh
T: +31 (0)639694482
When interested please react through the application process with your English resume.

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