Junior Clinical Trial Administrator

1 semana atrás

Lisboa, Lisboa, Portugal Lis Fortrea Development Ltd Sucursal Em Portugal Tempo inteiro

Junior Clinical Trial Administrator - FSP Team - Lisbon (Hybrid Position) page is loaded Junior Clinical Trial Administrator - FSP Team - Lisbon (Hybrid Position) Apply locations Lisbon Portugal time type Full time posted on Posted 6 Days Ago job requisition id As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas.

With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.


Job Overview:

The Clinical Trial Administrator (CTA) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project.

The degree of responsibility given to the CTA shall reflect their experience, and level of contribution which they can make to the project.

The CTA performs study-related tasks as required by the department, including (but not limited to): communicate with project team members regarding study updates, maintain documentation as required by protocols, SOPs and regulatory standards, to ensure timely production of high quality clinical data, provide systems support, track information related to the status of study activities and assist with general administrative functions as required.

Activities will be conducted in compliance with Company or Sponsor SOPs and regulatory standards and guidelines applicable.

Summary of Responsibilities:

  • Document and track study activities using relevant forms and tools, as well as relevant Project Management Systems with guidance/support.
  • Assist in the preparation of study and site-specific materials in accordance with relevant SOPs.
  • Complete minute taking and documentation for sponsor/external or internal teleconferences as requested.
  • Assist in setting up and maintaining tracking systems/spreadsheets for e.g., study supplies.
  • Maintain the Project Directory.
  • Provide support for Investigator Meetings; track meeting attendees and/or other information regarding the Investigator Meeting.
  • Provide support to project team (e.g., proof-reading and editing correspondence, mailings, shipping of study files, faxing and photocopying documents, assembling study documents, and arranging meetings, etc.).
  • Maintain Trial Master File documentation within the appropriate TMF platform, participate in TMF QC, as assigned, and track and /archive as applicable.
  • Audit and CAPA tracking.
  • Set up and maintain clinical investigator files and documentation.
  • Liaise with vendors, as needed, for study conduct such as printing study materials and/or external systems access for study team members.
  • Coordinate and plan study supply shipments with vendors.
  • Maintain and confirm shipment information such as courier tracking numbers and date of shipping and delivery.
  • Prepare/assemble/ship supplies to sites pre-SIV: Study File Notebooks, CRFs, other study-specific ancillary supplies (i.e., diary cards, patient visit reminders).
  • Generate reports as needed, for example CTMS site contact information list.
  • Work with the In-House CRA and other project team members on reconciliation of data with CTMS.
  • General communications to sponsors, sites and internal team members via electronic mail or courier or telephone.
  • Perform other administrative duties as assigned by Line Manager, Project Managers or Clinical Trial Lead.
  • All other duties as needed or assigned.

Qualifications (1 years of experience as CTA Required):

  • Diploma – Associate degree or equivalent.
  • In lieu of the above requirement, candidates with 1-2 or more years of relevant Clinical Research experience in pharmaceutical or CRO industries may be considered.
  • Fortrea may consider relevant and equivalent experience in lieu of educational requirements.

Language Skills Required:

Speaking:
English and local language

Writing/Reading:
English and local language

Experience (Minimum Required):

  • Minimum one (I) year administrative experience or equivalent training.
  • Good oral and written communication skills.
  • Good organizational and time management skills.
  • Computer literacy (Microsoft Office Suite (Word, Excel, PowerPoint)

Preferred:

  • Aptitude for handling and proof-reading numerical data, some spreadsheet software competency
  • Good typing skills
  • Good spelling and proof-reading skills
  • Ability to operate standard office equipment (e.g., fax, copier)
Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials.

Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need.

Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact.

For more information about Fortrea, visit
Fortrea is proud to be an

Equal Opportunity Employer:

As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind.

We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic.

We encourage all to apply.
For more information about how we collect and store your personal data, please see our Privacy Statement .

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