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Clinical Trial Assistant - CTA - with Spanish
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Clinical Trial Assistant - CTA - with Spanish

Rodzaj pracy
Pełny etat
Doświadczenie
Specjalista/Mid
Forma zatrudnienia
B2B, UoP
Tryb pracy
Praca hybrydowa
Ryvu Therapeutics

Ryvu Therapeutics

Ryvu Therapeutics is a clinical-stage drug discovery and development company focused on novel small molecule therapies that address emerging targets in oncology.

Zobacz profil pracodawcy

Wymagane umiejętności

spanish

eTMF

GCP

Opis stanowiska

Ryvu Therapeutics is a clinical stage biotechnology company developing novel small molecule therapies addressing high value emerging targets in precision oncology. With a mission to bring life-saving innovations to patients worldwide, we combine scientific excellence with a collaborative, forward-thinking culture. Join us in our mission to revolutionize oncology treatment.

 

Clinical Trial Assistant will work closely with the Clinical Operations team members by providing support to the conduct of clinical trials in day-to-day execution of clinical studies.


KEY RESPONSIBILITIES

  • Work closely with Clinical Operations team members to ensure successful clinical trial planning, execution and delivery.
  • Assist in study team meetings preparation. Issues and provides to an indicated team internal study team meeting minutes
  • Perform study related administrative tasks to support the Clinical Operations team as needed.
  • Track and reconciliation of study related materials e.g., study samples and investigational medicinal product
  • Assist in maintenance of study related tracking tools.
  • Assist in preparation of study specific documents, including finalization, distribution, document revision, management and archiving.
  • Assist with review of Trial Master File (eTMF) for completeness and timely provision of TMF content.
  • Assist with quality control checks for key study related materials e.g. protocols, study reports.
  • Contribute to department initiatives to improve the efficiency and effectiveness of the Clinical Operations team.
  • Support identification of vendors and collaborators
  • Support CTM and CRA to ensure successful clinical trial planning, execution and delivery.
  • Provide CTM and CRA with reports, trackers, summaries as required in the study.


YOUR BACKGROUND

  • Master's degree in the life sciences, chemistry or health related fields
  • Min 1 year experience at CRO, pharma or biotech organisation in a similar role.
  • Knowledge of intermediate Ms Office (Excel, Word, Powerpoint, Outlook) and internet-based systems (WebEX, SharePoint, etc).
  • Fluent English and Spanish
  • Current GCP training (must have)


YOUR BENEFIT PACKAGE

  • Work in one of the most innovative companies in the region with a proven track record and high perspective of growth
  • Participation in challenging and ambitious projects and opportunity for rapid scientific and business career development
  • Collaborative and supportive work culture
  • Training program enabling scientific development: Ryvu Academy, scientific lectures, participation in conferences
  • Package of benefits: Luxmed, Multisport and many others
  • Onsite support for foreigners and help with relocation if needed
  • Mindgram - wellbeing platform

 

 

If you don’t see yourself meeting every single requirement in the job posting, we still encourage you to apply. Research has shown that women and underrepresented groups often hesitate to apply unless they feel 100% qualified, but we believe that your unique experiences and perspectives matter. We’re committed to building an inclusive, diverse, and supportive workplace, and we warmly welcome applicants of all genders, backgrounds, cultures, abilities, and life experiences to join us.

 

Whistleblowing policy  


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