DSMB Member – Dermatologist

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🔥 1 minute ago

🐊 Florida – Remote

🐊 Florida – Remote

💵 $2k / day

⏳ Contract/Temporary

🟡 Mid-level

🟠 Senior

👻 Ghost score 0%

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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Sitero

WebsiteLinkedInAll Job Openings

201 - 500 employees

🏥 Healthcare

💼 Consulting

⚕️ Healthcare Insurance

Healthcare • Consulting • Healthcare Insurance

Sitero is a next-generation clinical trial solutions provider that accelerates clinical trials, ensures compliance and safety, and enables innovation through advanced technology and world-class services. They offer a wide range of clinical services, including site support and activation, data management, biostatistics, and drug safety. Sitero specializes in eClinical technology, providing end-to-end, technology-enabled services such as electronic data capture, randomization and trial supply management, clinical trial management systems, electronic consent solutions, and payment systems. Their services also include IRB ethical review, biosafety consulting, and pharmacovigilance agreements, ensuring comprehensive support for clinical research organizations.

📋 Description

• Review research submissions for regulatory, ethical, and institutional compliance • Prepare for and actively participate in scheduled meetings • Evaluate risks, benefits, and safeguards within research protocols • Identify non-compliance, protocol deviations, or safety concerns • Maintain confidentiality of sensitive research information • Provide recommendations for approval, modification, suspension, or termination of studies • Document reviews and determinations in accordance with institutional policies • Remain current with applicable regulations, guidance, and best practices • Complete required training and conflict-of-interest disclosures • Review interim study data for participant safety and data integrity • Assess adverse events, trends, and stopping rules • Recommend continuation, modification, or termination of trials • Maintain independence from study sponsors and investigators • Evaluate statistical analyses and safety monitoring plans • Ensure confidentiality of interim data and deliberations • Attend scheduled meetings, conduct independent review time before meetings, and participate in ad hoc reviews or urgent matters when needed

🎯 Requirements

• Advanced degree or equivalent experience in science, medicine, research ethics, regulatory affairs, biostatistics, veterinary medicine, biosafety, or related field (requirements vary by committee) • Board-certified physician with expertise in hair disorders and the diagnosis and management of androgenetic alopecia (AGA) • Demonstrated clinical and research experience in the evaluation and treatment of hair loss conditions, particularly androgenetic alopecia • Previous experience serving as an investigator, sub-investigator, medical monitor, or oversight committee member for androgenetic alopecia clinical trials • Familiarity with efficacy and safety endpoints commonly used in hair restoration and hair growth studies, including photographic assessments, hair density measurements, and patient-reported outcomes • Experience reviewing safety and efficacy data from dermatology or hair-loss clinical research programs • Ability to provide expert clinical interpretation of emerging study data and assess potential risks and benefits for study participants • Prior experience serving on a Data and Safety Monitoring Board (DSMB), Safety Review Committee (SRC), or similar independent oversight body preferred • Strong understanding of regulatory and ethical considerations related to clinical research involving dermatologic and hair-loss therapies

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