Senior CRA, German/French or German/Italian Speaking

🔥 1 minute ago

🇨🇭 Switzerland – Remote

⏰ Full Time

🟠 Senior

✨ German

👻 Ghost score 10%

infoinfo

🗣️🇩🇪 German Required

🗣️🇮🇹 Italian Required

🗣️🇫🇷 French Required

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Logo of Syneos Health

Syneos Health

10,000+ employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. By utilizing advanced technologies and insights, Syneos Health collaborates with clients to speed the delivery of important therapies to patients worldwide, offering services that span the entire clinical-to-commercial spectrum.

📋 Description

• Perform site qualification, site initiation, interim monitoring, site management and close-out visits on-site or remotely • Ensure regulatory, ICH-GCP/GPP and protocol compliance • Evaluate site and site staff performance and recommend site-specific actions • Escalate serious issues and develop action plans • Verify informed consent processes and protect subject/patient confidentiality • Assess subject/patient safety, protocol deviations/violations and pharmacovigilance issues • Conduct source document review and verify clinical data accuracy and completeness • Resolve queries remotely and on site within agreed timelines • Use hardware and software to support clinical study data review and capture • Verify compliance with electronic data capture requirements • Manage investigational product inventory, reconciliation, storage, security and dispensing as applicable • Review Investigator Site Files and reconcile them with Trial Master Files • Document monitoring activities and enter observations, status and action items into tracking systems • Support subject/patient recruitment, retention and awareness strategies • Manage site-level activities and communications to meet project objectives, deliverables and timelines • Liaise with project site personnel and ensure assigned sites and team members are trained and compliant • Prepare for and attend Investigator Meetings, sponsor meetings and clinical training sessions • Support audit readiness and audit follow-up actions • Provide training or mentorship to junior CRAs and perform training/sign-off visits as assigned • Perform clinical operations lead tasks under supervision when assigned

🎯 Requirements

• Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience • Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements • Strong monitoring experience in Switzerland • Good computer skills and ability to embrace new technologies • Excellent communication, presentation and interpersonal skills • Basic level of critical thinking skills • Proficient in English • Native-level German is essential • Italian or French speaking • Ability to manage required travel of up to 75% on a regular basis

🏖️ Benefits

• Career development and progression • Supportive and engaged line management • Technical and therapeutic area training • Peer recognition • Total rewards program • Inclusive culture • Reasonable accommodations when appropriate

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