Clinical Trial Associate - Barcelona, España - Labcorp

Labcorp

Empresa verificada

Barcelona, España

hace 2 semanas

Publicado por:

Isabel García

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Descripción

Minimum requirements:

Minimum of one (1) year previous industry experience (other professional and/or educational experience may contribute toward this requirement)
Basic understanding of biology and biological processes
Ability to monitor study sites according to protocol monitoring guidelines, SOPs, ICH Guidelines and GCP
Good organizational and time management skills
Good communication skills, oral and written
Exhibit general computer literacy
Works efficiently and effectively in a matrix environment
Fluent in local official language and in English, both written and verbal

Essential Job Duties:

Maintain and archive study files and communications both electronically and hard copy
Update electronic study data trackers and databases for assigned studies
Function as a liaison between Sponsors, CROs, Investigator sites, study vendors, Mobile Clinicians and/or Country Coordinators to communicate MCS services and activities on an as needed basis
Provide routine study status reports internally, as applicable
Secure Mobile Clinicians, including the qualification, credentialing, contracting of Home Health Agencies, and update applicable company databases (as required per region)
Communicate with Country Coordinators and/or Mobile Clinicians to confirm visits are scheduled and conducted as ordered on the Service Request Form
Train and manage Country Coordinators and/or Mobile Clinicians in their roles for specific studies to ensure compliance with study requirements
Review ambulant care documents provided by Country Coordinators and/or Mobile Clinicians to ensure their quality, completeness, and timely provision to the Investigator site as applicable
Resolve data inconsistencies or queries with Sponsors, Investigator sites, Country Coordinators and Mobile Clinicians, and work towards resolution
Review and interpret protocols and assist with or contribute to the development of training manuals and ambulant care documents for clinical studies
Understand amended protocols and other study manuals in order to identify changes that impact ambulant care services, and create Changes in Scope of Work documents
Participate in project teleconference calls and meetings as requested
Create and distribute agendas and minutes in a timely manner for teleconference calls and meetings
Maintain an inventory of study supplies, as applicable, such as laboratory kits for home visits
Assemble study specific laboratory kits, including shipping and arrangement of courier services as applicable
Train new staff in MCS procedures and specific studies
Participate in process improvement initiatives
Provide administrative support to MCS team members
Perform other related duties and tasks as necessary or assigned
Comply with ICH/GCP guidelines, GDPR and patient data protection laws, applicable SOPs and Process Guidelines, and study requirements
Adhere to contracted scope of work per signed agreement with the client

Labcorp is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, Labcorp 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.

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