Scientific Liaison

at  Cerba Research

9000 Ghent, Oost-Vlaanderen, Belgium -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate12 Feb, 2025Not Specified13 Nov, 2024N/AGood communication skillsNoNo
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Description:

As Scientific Liaison, you are the scientific operational intermediate between our Global Clinical Operations and Logistics department and our network of partner laboratories. You are the primary point of contact for scientific operational follow-up related to lab tests.
Your excellent organizational skills allow you to easily switch between i) providing daily operational support, ii) working on scientific projects, and iii) maintaining an overview on lab-specific issues (e.g. way of working, quality system, validation status, etc). Your hands-on mentality and solid scientific background allow you to confidently provide customer-oriented support.

Responsibilities:

LABORATORY SPECIFIC RESPONSIBILITIES

  • Being the point of contact between Cerba Research and the partner/subcontractor labs for scientific operational follow-up.
  • Manage lab changes by liaising with internal stakeholders to guarantee continuation of our services.
  • Upon award, you work closely with the sponsor and advise in defining the scope of validation as fit-for-purpose.
  • Improve the daily working relationships with our partner laboratories by acquiring an in-depth knowledge of their way of working, quality system, testing capabilities, etc.
  • Create and maintain relationships with our partner labs by informing them on pipeline projects, understand their main way of working, follow up on test validations, etc. This while communicating progress to relevant internal stakeholders.

INTERNAL SCIENTIFIC RESPONSIBILITIES

  • Address internal scientific questions (e.g. feasibility requests, questions regarding instruments and reagents, operational follow-up related to reporting and deviations, etc.) from various internal stakeholders (e.g. project management, sales, sample handling, etc)
  • Review and issuance of scientific material used by other internal departments
  • Assist operational teams during set up of clinical trials and provide checks, when needed, before results can be released
  • QA assistance during audits, lab related deviation or issuance and follow-up of CAPA’s
  • Prepare and provide ad hoc scientific trainings for our internal departments
  • Prepare and issue policies, procedures and working instructions to ensure documentation and optimization of operational flow
  • You provide training and development opportunities for team members to enhance their skills and knowledge, ensuring they are equipped to meet project requirements.
  • You stay abreast of relevant regulations and guidelines governing scientific research and ensure compliance throughout all operational activities.
  • You implement and maintain local quality assurance processes to adhere to local and international regulations.
  • Compliance with the Cerba Research Policies, Standard Operating Procedures, Work Instructions and other procedural documents relevant to the role.
  • Other tasks as defined by the Head of Department (HOD) necessary to complete the role.


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

Biology, Chemistry

Proficient

1

9000 Ghent, Belgium