SENIOR CLINICAL CONSULTANT – LIFE SCIENCES

CPL TAYLOR by Synergos srl - Ricerca e Selezione Personale Qualificato; Ciampino; Ibrido; EUR 50.000 - 70.000; Tempo pieno

Descrizione del lavoro

A consulting firm specializing in Life Sciences seeks a Senior Clinical Consultant to support digital transformation for clients in the pharmaceutical and biotech sectors. The role involves coordinating project milestones, implementing digital solutions, and ensuring compliance with regulatory standards. Ideal candidates will have a degree in Bioinformatics, professional English proficiency, and familiarity with clinical operations workflows. This permanent, full-time position offers flexibility with locations in Rome, Verona, or Milano.

Servizi

Dynamic, innovative environment

Opportunities to work in major cities

Competenze

• Degree in Bioinformatics or a related field.
• Professional English proficiency.
• Familiarity with ICH-GCP and regulatory requirements.

Mansioni

• Support clients in digital clinical transformation.
• Coordinate project milestones and deliverables.
• Implement clinical digital solutions and monitor activities.
• Prepare and maintain project documentation.
• Identify continuous improvement opportunities.

Conoscenze

Professional English proficiency

Familiarity with ICH-GCP

Knowledge of clinical operations workflows

Experience with clinical digital platforms

Formazione

Degree in Bioinformatics or a related field

Strumenti

EDC

eTMF

CTMS

SCE

Descrizione del lavoro

JOB SUMMARY

Senior Clinical Consultant – Life Sciences (Rif. ANN418147)

We are CPL & Taylor by Synergos, an international digital‑solutions consulting firm specialising in the Life Sciences sector. Based in Italy, we support pharmaceutical and biotech companies across regulatory, pharmacovigilance, clinical trials, medical affairs and quality assurance. The role is full‑time, permanent and open to candidates from Verona, Milano and Roma.

RESPONSIBILITIES

• Support clients in digital clinical transformation—planning projects, gathering requirements and monitoring deliveries to ensure compliance with regulatory standards, internal procedures and best‑practice.
• Coordinate project milestones and deliverables, ensuring on‑time delivery and maintaining documentation throughout the project lifecycle.
• Implement clinical digital solutions such as eTMF, CTMS and SCE, organising projects, documenting processes and monitoring activities.
• Prepare and maintain project documentation (kick‑off presentations, result sharing), conduct gap analyses and develop strategic roadmaps.
• Identify continuous improvement opportunities, collect feedback and propose enhancements to processes and methodologies.
• Assist in change management and hyper‑care activities for implemented systems.
• Facilitate stakeholder communication between internal teams, clients and partners.
• Triage client requests and issues during project execution, ensuring proper escalation.
• Define project KPI and support monitoring of project progress.

QUALIFICATIONS

• Degree in Bioinformatics or a related field.
• Professional English proficiency.
• Familiarity with ICH‑GCP and regulatory requirements, notably ICHE6(R3).
• Knowledge of clinical operations workflows (study start‑up, site management, monitoring, trial master file management).
• Experience with clinical digital platforms (EDC, eTMF, CTMS, SCE).

COMPANY & BENEFITS

• Contract: permanent, full‑time.
• Compensation: negotiated based on experience.
• Dynamic, innovative environment with strong focus on regulated markets.
• Opportunities to work in Rome, Verona or Milano.

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CONTACT

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