Senior Regulatory Coordinator

Emploi pas sur LinkedIn

🕒 il y a 1 mois

🇺🇸 États-Unis – Télétravail

💵 $44 - $69 / heure

⏰ Temps Plein

🟠 Senior

🚔 Conformité

🦅 Parrain de Visa H1B

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Foundation

Site WebLinkedInTous les Emplois

11 - 50 employés

₿ Crypto

🏪 Place de marché

🛍️ eCommerce

💰 €200 000 Seed Round en 2021-02

Crypto • Marketplace • eCommerce

Foundation est une plateforme qui facilite le commerce des tokens non fongibles (NFTs), mettant en avant des œuvres d'art et des illustrations numériques inspirées par des thèmes cosmiques et transformateurs. Elle permet aux artistes de créer, vendre et exposer leurs œuvres dans un marché en plein essor, en se concentrant sur l'intersection de la créativité et de la technologie. La plateforme embrasse la nature évolutive de l'art en rapport avec le paysage numérique, notamment à travers le prisme des NFTs et de la technologie blockchain.

Description

• Leads regulatory oversight for clinical trials, including preparation and submission of amendments, continuing reviews, safety reports, deviations, and study close-out documentation to IRB, DSMC, PRMC, IBC, and other regulatory committees while ensuring compliance with institutional and federal guidelines. • Maintains accurate and audit-ready electronic regulatory binders and essential study documents, ensuring ongoing compliance with GCP, protocol requirements, regulatory standards, and internal policies during monitoring visits and external audits. • Serves as a primary regulatory liaison between investigators, research teams, sponsors, CROs, and regulatory agencies, facilitating timely protocol approvals, resolving study-related questions, and communicating submission status updates to key stakeholders. • Provides regulatory expertise and operational guidance to investigators and research staff by leading onboarding, training, educational sessions, and development of reference materials related to clinical trial policies, procedures, and compliance requirements. • Collaborates with legal teams, sponsors, and study personnel to review informed consent documents, ensure consistency in institutional and contractual language, and implement protocol and staffing updates as required. • Participates in departmental meetings, process improvement initiatives, and cross-functional workgroups to enhance regulatory operations, strengthen compliance practices, and support efficient clinical research program execution.

🎯 Exigences

• Associates degree and 5 years of experience related to the management and conduct of clinical trials in an academic setting OR Bachelor’s degree and 3 years of experience related to the management and conduct of clinical trials in an academic setting. • Working knowledge of clinical trials, Federal, State, and Local Regulations, IRB requirements, consent form and protocol development.

🏖️ Avantages

• Comprehensive Benefits