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Benefits offered by this job
Career development opportunities
Supportive management
Diversity and inclusion culture
Job summary
A leading biopharmaceutical solutions organization in Spain seeks a Clinical Research Associate (CRA) to oversee monitoring activities across clinical research studies. Responsibilities include performing site qualifications, ensuring compliance with regulations, and documenting site interactions. The ideal candidate holds a Bachelor's degree or RN and possesses strong communication and computer skills. The position may require up to 75% travel. This is a prospective opportunity, adding candidates to the talent pipeline for upcoming roles.
Qualifications
Demonstrates good computer skills and embraces new technologies.
Must manage required travel of up to 75% regularly.
Knowledge of regulatory requirements is essential.
Responsibilities
Performs site qualification, initiation, monitoring, and close-out visits.
Assures informed consent process is documented for each subject/patient.
Documents activities using confirmation letters, reports, and logs.
Skills
Good Clinical Practice/ICH Guidelines
Excellent communication
Good computer skills
Interpersonal skills
Education
Bachelor’s degree or RN in a related field
Job description
A leading biopharmaceutical solutions organization in Spain seeks a Clinical Research Associate (CRA) to oversee monitoring activities across clinical research studies. Responsibilities include performing site qualifications, ensuring compliance with regulations, and documenting site interactions. The ideal candidate holds a Bachelor's degree or RN and possesses strong communication and computer skills. The position may require up to 75% travel. This is a prospective opportunity, adding candidates to the talent pipeline for upcoming roles.