Senior Clinical Research Associate

📋 Description

• Conducts on-site or remote monitoring activities for Pre-Study, Initiation, Interim, and Close-Out to ensure that the investigational site’s facilities and staff are suitable for the study's execution.

• Identifies investigators and confirms that they possess the necessary qualifications, resources, facilities, equipment, and personnel to carry out the clinical study throughout its duration.

• Provides training to investigational site personnel as required.

• Assists in the preparation of regulatory and/or ethics committee submissions when applicable.

• Engages in mentoring and training of new team members and conducts co-monitoring visits to evaluate the performance of junior staff.

⛳️ Requirements

• A college or university degree in Life Sciences or a comparable combination of education, training, and experience.

• Significant on-site monitoring experience in phase 2/3 clinical trials, preferably with a focus on complex trials in oncology or rare diseases.

• Full working proficiency in English.

• Strong planning, multitasking abilities, and capability to thrive in a dynamic team environment.

• Excellent communication, collaboration, and problem-solving skills.

• Willingness to travel nationally.

🏝️ Benefits

• Opportunities for training and career development within the organization.

• A strong focus on personal and professional advancement.

• A friendly and supportive workplace culture.

• The chance to collaborate with colleagues from around the globe, with English as the primary company language.