Senior Clinical Research Associate

Job not on LinkedIn

🔥 1 hour ago

🇺🇸 United States – 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.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

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 according to the protocol, SOPs, ICH-GCP, and applicable regulatory requirements • Conduct site qualification, initiation, monitoring, and close-out visits according to monitoring plans, sponsor and company SOPs, ICH/CGP 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 data collection and regulatory document collection are adequate

🎯 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 • Applicants must be legally able to work in the US

🏖️ Benefits

• Permanent full-time position • Vacation • Sick days • 401K • Benefits • Travelling position with teleworking allowance • Ongoing learning and development • Attractive advancement opportunities