Manager, Records Management – TMF Quality Control Specialist

Vaga não está no LinkedIn

🕒 Maio 5

🏄 California – Remoto

🏄 California – Remote

💵 $115.000 - $145.000 / ano

⏰ Tempo Integral

🟢 Júnior

🟡 Pleno

👔 Gerente

Candidatar-se

Encontrar Vagas Remotas Similares

Receber Emails de Vagas Remotas

📊 Verifique sua pontuação de currículo para esta vaga

Melhore suas chances de conseguir uma entrevista verificando sua pontuação de currículo antes de se candidatar.

Enviar Currículo

Codera

SiteLinkedInTodas as Vagas

11 - 50 funcionários

🧬 Biotecnologia

💊 Farmacêutico

🤝 B2B

Biotechnology • Pharmaceuticals • B2B

A Codera é uma empresa B2B que faz parceria com empresas de biotecnologia e farmacêuticas para fornecer expertise e infraestrutura de desenvolvimento de medicamentos de ponta a ponta. Ela apoia clientes em todo o ciclo de vida do desenvolvimento de medicamentos com serviços técnicos, operacionais e infraestrutura para ajudar a avançar os programas terapêuticos.

Descrição

• Provide support for TMF activities by ensuring documents uploaded to the TMF adhere to Standard Operating Procedures, ICH GCP guidelines and other regulatory requirements • Act as a TMF Subject Matter Expert (SME) and work with the study teams to ensure the TMFs and CTMS for clinical studies are inspection ready at all times • Review study documents received from the study teams for completeness and accuracy and upload to the Trial Master File (TMF) • Perform quality control of documents submitted to the TMF per SOPs, Work Instructions and Guidance Documents • Ensure documents which fail TMF quality control and/or TMF quality review are effectively remediated and provide best practice recommendations, as needed • Conduct TMF educational workshops/training, as needed • Address TMF questions pertaining to how documents are filed, and user questions related to the TMF system • Ensure Essential Document Lists (EDLs) are maintained on an ongoing basis • Perform the secondary review of site Essential Document Packages per applicable SOPs to ensure sites meet the requirements for site activation and Investigational Product (IP) release • Responsible for Clinical Trial Management System (CTMS) maintenance, including study, country and site level updates and reviewing CTMS entries for accuracy • Contribute to TMF QC Tools as needed to match with evolving business processes (incl. QC Tool, QC Manual, Doc Owner Manual, TMF Newsletters) • Maintain up to date knowledge of the TMF Reference Model, industry best practices and regulatory considerations as applicable to the job duties • Assist with inspection/audit related activities (e.g., preparation, corrective action plans)

🎯 Requisitos

• Minimum 2 years of relevant clinical research and TMF experience required • Understanding of the clinical trial process, experience in handling clinical trial related documents required • Previous experience in electronic TMFs, Veeva preferred • Strong knowledge of ICH-GCP guidelines and regulatory requirements related to clinical document management • Must be self-motivated, well-organized, detail-oriented, and have excellent written and verbal communication skills • Demonstrated ability to achieve high performance goals and meet deadlines in a fast-paced environment • Strong organization skills with outstanding attention to detail and follow-through • Must be highly resourceful and adaptable to effectively support multiple competing demands and changing priorities • Demonstrated proactive approaches to problem-solving with strong decision-making capabilities • Must be fully proficient in MS Office Suite and internet research.

🏖️ Benefícios

• employer sponsored insurance plans including medical, dental and vision coverage • generous paid time off • retirement plan options • additional wellness and professional development programs