Clinical Research Associate (CRA) II

at  Medicorent

Clinical Research Associate (CRA) II, Sweden
Medicorent is a Scandinavian contract research organization providing innovative full-service solutions to the pharmaceutical industry in the Nordics and some European countries. With a close network of over 100 active consultants and access to a great number of candidates in the life-science area, we take care of internal projects as well as offering long- and short-term outsourcing solutions to our clients. We are committed to quality and cost-effectiveness to help our clients and partners deliver life-changing therapies and improve health and well-being.
We have a new opening for a Clinical Research Associate II for our operations.
This is a permanent position and can be office/home-based in Stockholm and will be assigned to both external and internal projects.

QUALIFICATIONS AND EXPERIENCE:

• Bachelor’s degree in life or health sciences, preferably with a nursing background and experience in intensive care.
• Minimum 2 years of experience conducting clinical trials in the pharmaceutical, biotech, or CRO industry
• In-depth knowledge of ICH-GCP
• Fluent in Swedish and English
• Proven flexibility and adaptability
• Experienced user of MS Office suite
• Willingness and ability to travel across Sweden and occasionally to other European countries

Plan and properly conduct clinical trials in accordance with protocol, SOPs, local procedures, national regulations/requirements, and ICH-GCP including:

• Submit and obtain necessary approvals from the authorities
• Perform site selection, initiations, monitoring, and source data verification (SDV)
• Manage site recruitment performance
• Oversee trial supplies management
• Conduct data cleaning activities
• Manage study close-out and archivin

Plan and properly conduct clinical trials in accordance with protocol, SOPs, local procedures, national regulations/requirements, and ICH-GCP including:

• Submit and obtain necessary approvals from the authorities
• Perform site selection, initiations, monitoring, and source data verification (SDV)
• Manage site recruitment performance
• Oversee trial supplies management
• Conduct data cleaning activities
• Manage study close-out and archiving