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Senior Clinical Research Specialist

Remote: 
Full Remote
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Offer summary

Qualifications:

5+ years of clinical research experience, Experience with audits and CAPAs, Knowledge of risk management and ISO 14155, Bonus: Experience in LAAC/structural heart..

Key responsabilities:

  • Maintain and implement Standard Operating Procedures (SOPs) using existing templates
  • Ensure training is up to date and clinical compliance is met
  • Prepare for and respond to audits, including post-audit CAPAs
  • Manage risk associated with clinical research activities.

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Real Staffing http://www.realstaffing.com
201 - 500 Employees
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Job description

We have a current opportunity for a Senior Clinical Research Specialist on a contract basis. The position will be based in New Brunswick. For further information about this position please apply.

Senior Clinical Research Specialist

Day to Day: Maintain SOPs, Implement SOPs using existing templates, ensure trainings are up to date, clinical compliance, risk management. Audit (prep, post, response - CAPAs). They are anticipating both a system and site audit.

Experience:
5+ years of clinical research experience
Experience with audits/CAPAs
BONUS: LAAC/structural heart experience

Desired Skills and Experience

5+ years of experience in Clinical Research
Audit/CAPA
Risk management
ISO 14155

EOE Statement: Specialist Staffing Group is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.



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Experience

Spoken language(s):
English
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