Senior Clinical Data Specialist - Hybrid Remote

Ctifacts; Lisboa; Híbrido; EUR 35 000 - 55 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Health benefits

Hybrid work from home opportunities

Paid parental leave

Tuition reimbursement

Resumo da oferta

CTI Clinical Trial and Consulting Services in Lisboa, Portugal, is seeking candidates with a strong background in clinical data management and relat ional databases. You will review CRF data, manage study files, ensure data integrity, and contribute to SOP development within a GMP-compliant framework.

The role requires 3–4 years in data management, 2 years of relational database experience, and a Bachelor’s degree in biology, behavior, or computer science.

Qualificações

• 3 to 4 years clinical data management experience in any capacity.
• 2 years relational database experience.
• Bachelor’s Degree or equivalent in biological, behavioral, or computer science.

Responsabilidades

• Conduct pre-entry review of clinical data.
• Review and issue queries for CRF data based on edit checks and sponsor requirements.
• Assist with set-up of data management study files and archiving of study documentation.
• Maintain documentation to support accuracy and integrity of clinical databases.
• Assist in tracking controlled documents (CRFs, DCFs, etc).
• Define workflow and processes for all aspects of data management.
• Collaborate with management to develop SOPs relating to data management.
• Conduct and direct database development, testing, and validation.
• Conduct and direct training of clinical data associate staff.
• Adhere to CTI SOPs and GCP/ICH guidelines to ensure quality.

Conhecimentos

Clinical data management

Relational databases

Quality management

Formação académica

Bachelor’s Degree or equivalent in biological, behavioral, or computer science

Descrição da oferta de emprego

CTI Clinical Trial and Consulting Services in Lisboa, Portugal, is seeking candidates with a strong background in clinical data management and relat ional databases. You will review CRF data, manage study files, ensure data integrity, and contribute to SOP development within a GMP-compliant framework.

The role requires 3–4 years in data management, 2 years of relational database experience, and a Bachelor’s degree in biology, behavior, or computer science.