Senior Clinical Research Associate, Dermatology – Rheumatology

Job not on LinkedIn

🔥 13 hours ago

🇵🇱 Poland – Remote

⏰ Full Time

🟠 Senior

🧪 Clinical Research

👻 Ghost score 12%

What it means: how likely this posting is sitting open without active hiring.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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Innovaderm Research Inc.

WebsiteLinkedInAll Job Openings

201 - 500 employees

💊 Pharmaceuticals

🏥 Healthcare

💼 Consulting

Pharmaceuticals • Healthcare • Consulting

Innovaderm Research Inc. is a Contract Research Organization (CRO) specialized in dermatology, providing scientific guidance and conducting Phase I to IV clinical trials in the field. With a strong presence in North America and Europe, Innovaderm offers a comprehensive range of services including study design, regulatory consulting, project management, patient recruitment, and data management, ensuring high-quality research outcomes and customer satisfaction since 2000.

📋 Description

• Monitor the progress of clinical studies at investigative sites or remotely • Ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, SOPs, ICH-GCP, and applicable regulatory requirements • Conduct site qualification, initiation, monitoring, and close-out visits according to the monitoring plan, company and sponsor SOPs, ICH/GCP guidelines, and applicable regulations • Participate in investigators’ meetings • Prepare site visit reports and follow-up letters to investigators • Build productive relationships with investigators and site staff to achieve study objectives, including patient recruitment targets • Perform source data verification • Ensure adequate on-site study drug storage, dispensing, and accountability • Ensure adequate data collection and regulatory document collection

🎯 Requirements

• B.Sc. in a field relevant to clinical research, nursing degree and/or equivalent experience • 5 to 8 years experience in conducting on-site clinical monitoring in the biotechnology, pharmaceutical, and/or contract research organization (CRO) industry • Good knowledge of ICH/GCP standards and applicable regulatory requirements • Strong verbal and written communication skills in English • Ability to prioritize different assignments and work under pressure while maintaining attention to detail and meeting timelines • Excellent judgement and problem-solving skills • Travel to research sites approximately 65% of the time • Excellent knowledge of Microsoft Office (i.e., Word, Excel, PowerPoint) • Experience in dermatology is an asset • Legally able to work in Poland

🏖️ Benefits

• Flexible work schedule • Permanent full-time position • Vacation, PPK, health allowance • Home-based position with teleworking allowance • Ongoing learning and development • Attractive advancement opportunities