ppPrimary Location bSpain /bbr/Job ID: bSP_MA-2411 /bbr/Job Type: bFull-Time /b /p h3JOB DESCRIPTION /h3 h3Your main responsibilities: /h3 ul liAssisting CRAs in their routine work; /li licompleting submission of documents to the Regulatory Authority (including safety reports) when required; /li lireporting safety data to Sponsor’s Pharmacovigilance Department and providing assistance when required; /li liperforming remote monitoring and site management; /li licollecting, reviewing and tracking regulatory documents when required; /li liperforming translations (only in case of appropriate education); /li liassisting with the completing of study specific documents, annotated Case Report Forms (CRFs), tracking forms, and other study /li lirelated documents; /li liparticipating in study specific training; /li liproviding status updates to CRAs and Project Manager; /li liparticipating in the preparation and coordination of investigator meetings; /li /ul h3You have:



/h3 ul liFluency in English and local language (written and spoken); /li lihigher education (a degree in science or a related field would be an asset); /li liknowledge of ICH-GCP and national regulations related to clinical trials; /li ligood to excellent verbal and written communication skills; /li licomputer literacy: skills of proficient work with MS Office; /li ligood to excellent organizational, record retention, decision making, customer service, and interpersonal skills; /li liability to establish and maintain effective working relationships with coworkers, managers and clients. /li /ul h3We offer: /h3 ul liCompetitive salary and benefits; /li liFlexible working arrangements; /li liCareer opportunities at local, regional and general levels; /li liSupport for personal and professional development (trainings, coaching, career development, international assignments, etc). /li /ul pWe provide equal opportunity to all qualified applicants and employees by prohibiting discrimination in employment decisions because of race, color, religion, sex, national origin, age, veteran status or disability. /p pCromos Pharma is an international contract research organization delivering integrated clinical research solutions that accelerate drug development. /p /p #J-18808-Ljbffr

📌 In-house CRA (España)
🏢 Cromos Pharma
📍 España