Case Processing Specialist

at  ClinChoice

Schleswig-Holstein, Schleswig-Holstein, Germany -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate26 May, 2024Not Specified01 Mar, 2024N/ATeamwork,Reporting Systems,Time Management,English,CollaborationNoNo
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Description:

ClinChoice is a global full-service CRO dedicated to professional development and providing an excellent work-life balance, with a quality-focused, collaborative “one-team” culture. We are looking for a dynamic person to join our in-house team as a Case Processing Specialist on a permanent basis. You will work on projects from our varied client base, ranging from small to big pharmaceutical, biotechnology, medical device and consumer health companies.
Join our team: you can be part of making a difference in peoples’ lives and experience a fulfilling and rewarding career!

EDUCATION, EXPERIENCE AND SKILLS:

  • Life Science/ Medical Graduates/Postgraduates
  • Pharmacovigilance Knowledge
  • Fluency in English
  • Adverse Event Reporting Systems
  • Attention to Detail
  • Time Management
  • Teamwork and Collaboration
  • Computer Proficiency

Responsibilities:

  • Receive and triage adverse events from various sources and ensure that the required information is collected and recorded.
  • Perform data case validity, data completion check, data encoding and quality review.
  • Perform adverse event coding as per MedDRA term selection.
  • Perform case narrative writing using predefined templates.
  • Perform the safety (seriousness, expectedness, and causality) assessment, quality review, medical safety assessment rationale and finalization of the case.
  • Complete deliverables according to the required form/template.
  • Timely notification to the client on the Reportable cases, based on regulatory requirements.
  • Ensure compliance with timelines, quality and training as specified in the SLA.
  • Support any additional quality gates as determined for the project.
  • Participate in process improvement initiatives to keep up the Quality and Compliance score.
  • Ensure all activities are carried out according to applicable control documents and project requirement.


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

Proficient

1

Schleswig-Holstein, Germany