Clinical Research Associate FREELANCE

JR Italy; Bari; In loco; EUR 30.000 - 50.000; Tempo pieno

Descrizione del lavoro

A Contract Research Organization is seeking a Clinical Research Associate to support their Operational Italian Team. This role offers a full remote work opportunity and requires a Bachelor's degree in a relevant field, clinical monitoring experience, and GCP-ICH training. Successful candidates will conduct site visits and ensure data integrity while working in a dynamic, multicultural environment.

Servizi

Full remote work opportunity

Multicultural and dynamic work environment

Competenze

• Proven experience in clinical monitoring with relevant training.
• Current CRA certification as per MoH decree 15/11/2011.
• Availability to travel in Central-South Italy.

Mansioni

• Conduct site visits according to SOPs and study Monitoring Plan.
• Write monitoring reports and perform site management.
• Check data integrity and support submissions to ethics committees.

Conoscenze

Clinical monitoring experience

Excellent organizational skills

Time management skills

GCP-ICH training

Bachelor's degree/MD in relevant field

Formazione

Bachelor’s degree/MD or equivalent in a technical-scientific field

Descrizione del lavoro

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Clinical Research Associate FREELANCE, Bari

Client:

Evidilya

Location:

Bari, Italy

Job Category:

Other

EU work permit required:

Yes

Job Reference:

8662617666420211712337117

Job Views:

3

Posted:

27.08.2023

Expiry Date:

11.10.2023

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:

Clinical Research Associate

To reinforce the Operational Italian Team.

Main Responsibilities:

• Conduct and perform SQV/Pre-study Visits, site initiation visits, monitoring visits, close-out visits, according to SOPs and study Monitoring Plan.
• Write Monitoring Reports and perform site management, addressing follow-up activities.
• Check data integrity.
• Support the team in the submission of the study to ethics committees/IRBs.

Hard & Soft Skills:

• Bachelor’s degree/MD or equivalent in a technical-scientific field.
• Proven experience in clinical monitoring and relevant training in the field.
• Proven GCP-ICH training.
• Current CRA certification as per MoH decree 15/11/2011.
• Excellent organizational and time management skills.

Additional requirements:

• Availability to travel, especially in Central-South Italy.

What we offer:

• Full remote work opportunity.
• Multicultural, young, and dynamic work environment.