Jr Clinical Trial Assistant (STAGE)

JR Italy; Milano; In loco; EUR 25.000 - 45.000; Tempo pieno

Descrizione del lavoro

An established industry player in clinical research is seeking a Junior Clinical Trial Assistant to join their dynamic team in Milan. This role involves supporting the study team throughout the project lifecycle, managing essential documentation, and ensuring compliance with protocols and regulations. Candidates should possess a Master's degree in a scientific or healthcare discipline and demonstrate strong organizational and decision-making skills. This is a fantastic opportunity to kickstart your career in a supportive environment, making a tangible impact on clinical trials and patient outcomes.

Competenze

• Master's degree in a scientific discipline or healthcare preferred.
• Strong organizational and decision-making skills.

Mansioni

• Collaborate and support the study team members for project execution.
• Prepare, manage, and archive study documents and reports.
• Evaluate the quality and integrity of study sites.

Conoscenze

Organizational Skills

Decision-Making Skills

Formazione

Master's Degree in a Scientific Discipline

Master's Degree in Healthcare

Descrizione del lavoro

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Jr Clinical Trial Assistant (STAGE), Milano

Client: Evidilya

Location: Milano

Job Category: Other

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EU work permit required: Yes

Job Reference:

590972830468800512033710

Job Views:

2

Posted:

26.04.2025

Expiry Date:

10.06.2025

Job Description:

Evidilya, the dedicated Contract Research Organization of Sprim Health Group, operates as a full-service international expertise in successfully developing and managing observational, pre-clinical, and clinical trials. We are looking for a:

Junior Clinical Trial Assistant (Stage)

to reinforce our Clinical Team in Milan.

Main Tasks:

• Collaborate and support the study team members for project execution from start to finish.
• Prepare, manage, share, and archive study documents and reports according to protocols, SOPs, and applicable regulations.
• Evaluate the quality and integrity of study sites, performing periodic reviews (TMF and TCF).
• Support CPM and CRA in developing and maintaining the Trial Master File and Trial Center Files.
• Assist the CPM by tracking regulatory submissions and approvals, recruitment and enrollment, CRF completion and submission, and data query resolution. Support start-up phase and onboarding of stakeholders and suppliers.
• Manage the relationship with the sponsor and update the CPM on the trial status.

Qualifications:

• Master's Degree in a scientific discipline or healthcare preferred.
• Strong organizational and decision-making skills.

Candidates are invited to send their CV and cover letter authorizing the processing of personal data pursuant to art. 13 of Regulation (EU) no. 2016/679 (