CRA II – Client Dedicated

🕒 September 28

🇩🇪 Germany – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🧪 Clinical Research

👻 Ghost score 16%

What it means: the chance that no one is really hiring for this job.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Syneos Health

WebsiteLinkedInAll Job Openings

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 • Evaluate site and site staff performance and provide site-specific recommendations • Communicate and escalate serious issues and develop action plans • Verify informed consent, subject/patient confidentiality, safety and clinical data integrity • Conduct source document review and verify CRF data accuracy and completeness • Resolve queries remotely and on site within agreed timelines • Verify compliance with electronic data capture requirements • Manage investigational product inventory, reconciliation, storage, dispensing and administration as applicable • Review and reconcile Investigator Site Files with the Trial Master File • Document monitoring activities through letters, trip reports, communication logs and project documents • Support subject/patient recruitment, retention and awareness strategies • Track observations, status and action items to resolution • Manage site-level activities, communications, project objectives, deliverables and timelines • Liaise with study site personnel and ensure site team training and compliance • Attend investigator, sponsor, clinical monitoring and training meetings • Support audit readiness, audit preparation and follow-up actions • Maintain knowledge of applicable guidelines, regulations and company SOPs and complete required training

🎯 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 • Good computer skills and ability to embrace new technologies • Fluency in German and English • Excellent communication, presentation and interpersonal skills • Location in South-West Germany, as Swiss sites are also to be supported • Ability to manage required travel of up to 75% on a regular basis • Experience conducting clinical monitoring activities • Ability to comply with protocols, regulations, ICH-GCP/GPP and company SOPs/processes

🏖️ Benefits

• Career development and progression • Supportive and engaged line management • Technical and therapeutic area training • Peer recognition and total rewards program • Inclusive culture • Global collaboration opportunities • Remote work arrangement (Remote (Pre-Approved))

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