Clinical Data Coordinator

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🔥 0 minutes ago

🇦🇷 Argentina – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

✨ Clinical Data Coordinator

👻 Ghost score 12%

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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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

• Participate in clinical data management activities to ensure clinical trial data are collected, managed and reported clearly, accurately and securely • Conduct activities in conformance with regulatory requirements, industry guidelines, Indero standard operating procedures, sponsor requirements and timelines • Provide general data management support to the project team, sponsor and external vendors • Support the Lead Data Manager with data review, data reconciliation and discrepancy management • Maintain study metrics and monitor study status, including enrollment and CRFs monitored/approved • Provide data status reports to the project team as needed • Generate ad-hoc study reports • Perform user maintenance • Assist with user acceptance testing • Assist with database design • Assist with creating data management plans and related documentation • Assist in ensuring data management documentation is complete and up-to-date in the trial master file

🎯 Requirements

• B.Sc. or related field • 1 year of clinical data management experience in the pharmaceutical industry or in a CRO environment is considered an asset • Experience using an EDC system (ie. Medidata Rave, Medrio) is considered an important asset • Skilled in use of computer technology, and ability to learn new applications • A general knowledge of CDASH/SDTM is considered an asset • Highly organized and detail-oriented with effective project planning and time management skills • Strong verbal and written communication skills in English; French is an asset • Ability to work in a fast-paced environment with demonstrated agility to juggle and prioritize multiple competing demands • Excellent interpersonal, communication, problem solving and organizational skills with the ability to work both independently and in a team environment • Understanding of the drug development process and of applicable regulations, including Good Clinical Practices, ICH Guidelines, and applicable Health Canada and Food and Drug Administration (FDA) regulations/guidelines • Must be legally authorized to work in Argentina

🏖️ Benefits

• Flexible work schedule / work schedule • Home-based position • Ongoing learning and development • Attractive advancement opportunities • Accommodations throughout the recruitment and selection process to applicants with disabilities, upon request

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