Auftragsdetails

Lead Clinical System Consultant - propharma group

Datum der Veröffentlichung: Mar 22, 2023
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Auftragsdetails

  • Ort:
    Overland Park, Kansas, United States of America
  • Gesellschaft:
  • Typ:
    Full Time/Permanent
  • Shift:
    First Shift (Day)
  • Karrierelevel:
    Experienced Professional
  • Positionen:
    4
  • Erfahrung:
    3 Year
  • Geschlecht:
    Keine Präferenz
  • Grad:
    Masters
  • Vorher bewerben:
    Nov 30, 2023

Job Summary

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.

Detailed Description

This position will play a core role in the design, roll-out, and maintenance of software solutions within the life sciences domain. While this is a remote full-time permanent role with ProPharma Group, the position is customer facing and may require up to 25% travel. Must be Veeva White Belt certified.

Essential Functions Include:

  • Manage software implementation projects and customers throughout the lifecycle of system adoption, focusing on project planning, gap analyses, workshop delivery, requirements gathering, configuration, validation, migration, integration, training, and go-live activities
  • Serve as the primary customer liaison managing communication, risks, go-live planning, and project reporting between the project team, customer, and internal stakeholders
  • Ensure customer success over the entire project
  • Mentor project team and consultants in the R&D Services organization and provide leadership for project teams
  • Collaborate cross-functionally with other teams across the company
  • Develop and finalize project and configuration mapping specifications, applying industry best practices
  • Configure Vault and other GxP Systems
  • Lead customer requirement development
  • Perform CSV/CSA and UAT
  • Function as clients trusted advisor and ensure client success throughout the project lifecycle
  • Escalate project risks and develop contingency plans as necessary
  • Ensure compliance with all regulatory and client-side requirements
  • SaaS/Cloud experience including knowledge of systems validation
  • Ability to understand and document end-user needs and functional requirements

 

Qualifications

Qualified candidates must have:

  • Minimum:  Bachelor’s degree in a relevant scientific or technology-focused discipline, plus five years’ experience in Biotech/Pharma IT. Master’s degree or Ph.D. in a relevant scientific or technology-focused discipline, plus four years’ experience in Biotech/Pharma IT
  • Must be Veeva White Belt Certified with at least two years of experience with one or more Veeva Vault applications
  • Experience in services delivery management and/or systems implementation
  • Experience in a customer-facing role, ideally in a consulting background
  • Self-motivated with proven ability to work independently, while concurrently working effectively in cross-functional teams
  • Proven track record of meeting project timeliness and producing high quality deliverables
  • Excellent verbal and written communication, interpersonal, and presentation skills, including ability to author SOPs and Job Aids and deliver end user training.
  • Understanding of the research and clinical technology landscapes within the life sciences domain
  • Ability to travel and work across multiple time zones (25%)

We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.

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Company Overview

Berlin, Berlin, Germany

ProPharma Group is the leading global, independent, single-source provider of regulatory, clinical, and compliance services serving the pharmaceutical, biotechnology, and medical device companies. Our team of experts brings a comprehensive portfolio... Read More

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