Document Specialist I - Ciudad de México - Fortrea

Fortrea

Empresa verificada

Ciudad de México

hace 1 semana

Publicado por:

Rodrigo Fernández

Reclutador de talento para beBee

Descripción

Clinical Document Specialist I - Remote

Are you looking for a fresh start within a clinical document environment? Interested in working within Clinical Pharmacology, working alongside our Project Management and Phase I Monitoring team, in an administrative and IT-focused opportunity?

Fortrea is seeking a Clinical Document Specialist to join the global Clinical Pharmacology Services team.

Perhaps you have some experience within a medical/life sciences environment but now looking to be home-based, managing documentation compliance across the clinical trial process.

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.

Key Responsibilities

Your main responsibilities will include but not be restricted to:

Responsible for general maintenance and any required archival of documents produced by the study project teams within CPS.
Organizing, gathering, scanning, and filing of all applicable documents into appropriate electronic and/or paper copy locations, including the Trial Master File (TMF), as directed by Fortrea SOPs or other applicable directive.
Responsible for document query generation and file reconciliation/resolution activities to support delivery of the TMF to client quality and integrity specifications, as well as to meet project timelines and productivity targets.
Maintains an internal standardized filing structure for study-related documents.
Works directly with the assigned Study Project Manager (PM) to review and finalise the TMF Plan and Index for individual projects.
Creates and/or maintains any general document/file-related tracking forms and/or spreadsheets, as applicable.
Maintains the TMF by working with applicable project team members to retrieve, file, and upload documents in accordance with applicable SOPs, policies, system, and client requirements.
May interact directly with project teams in securing documents for the TMF, as appropriate.
May interact directly with project teams to follow up regarding missing documents, as appropriate.
Performs archiving duties for all paper and/or electronic media, as needed.
Maintains departmental files including, but not limited to, project files.

Experience- Any experience within an administrative or IT-focused role within clinical trials or a hospital/medical setting would be advantageous. Full training will be provided.- Experience working with computers and basic programs (i.e., Adobe Acrobat, Word, Excel, PowerPoint).

Education / Qualifications- High School Diploma or equivalent.- Strong written and verbal communication skills (English language).- Strong organisational skills, with the ability to work in a fast-paced setting with many interruptions.

Did you know?

Fortrea is looking for problem-solvers and creative thinkers who are passionate about breaking down barriers faced by sponsors of clinical trials, and who are committed to helping transform the development process to get promising life-changing ideas and therapies to patients faster.

Join us as we cultivate a workspace where all employees have the opportunity to grow and make impacts on a global scale.

For more information and questions related to Fortrea, please visit

LI-Remote, Remote

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