[Hiring] Senior Clinical Research Associate @Ergomed

Role Description

• Performs on-site or remote Pre-Study, Initiation, Interim, and Close-Out monitoring visit activities to ensure that facilities and staff at the investigational site continue to be adequate for the conduct of the study.
• Identifies the investigators and verifies that the investigator has adequate qualifications, resources, facilities, equipment, and staff to conduct the clinical study throughout the study period.
• Trains investigational site staff as necessary.
• When applicable, supports preparation of regulatory and/or EC submissions.
• Participates in mentoring/training of new staff as well as performing co-monitoring visits, to assess junior staff performance.

Qualifications

• College/University degree in Life Sciences or an equivalent combination of education, training & experience.
• Extensive on-site monitoring experience in phase 2/3 trials, ideally with experience of complex trials in oncology or rare disease.
• Full working proficiency in English.
• Ability to plan, multitask and work in a dynamic team environment.
• Communication, collaboration, and problem-solving skills.
• Ability to travel nationally.

Benefits

• Make a difference by helping to bring safe and effective pharmaceutical treatment to patients around the world.
• Join a passionate and collaborative team of experts in clinical research, pharmacovigilance, and quality consulting.
• Diverse values that unite the team, including:
• Quality: we hold ourselves to the standard patients deserve.
• Integrity and trust: we do the right thing, especially when it is hard.
• Drive and passion: we care about the outcome, because someone is waiting on it.
• Agility and responsiveness: we move quickly, because patients cannot wait.
• Belonging: everyone is welcome, and every voice counts.
• Collaborative partnerships: we go further by going together.

Department

Clinical Monitoring