Senior Clinical Consultant – Life Sciences

CPL TAYLOR by Synergos srl - Ricerca e Selezione Personale Qualificato; Milano; In loco; EUR 50.000 - 70.000; Tempo pieno

Descrizione del lavoro

Una società di consulenza internazionale in Italia cerca un Senior Clinical Consultant per supportare le aziende farmaceutiche e biotech nella trasformazione clinica digitale. Il candidato ideale ha una laurea in Bioinformatica e competenze professionali in inglese. Responsabilità includono pianificazione progetti e implementazione di soluzioni cliniche digitali. La posizione è full-time e permanente, con possibilità di lavorare in diverse città tra cui Milano, Roma e Verona.

Competenze

• Laurea in Bioinformatica o in un campo correlato.
• Competenza professionale in inglese.
• Familiarità con ICH-GCP e requisiti normativi.

Mansioni

• Supporto ai clienti nella trasformazione clinica digitale.
• Coordinare traguardi e risultati del progetto.
• Implementare soluzioni cliniche digitali.

Conoscenze

Bioinformatics

Professional English proficiency

Clinical operations workflows

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

Centralino Unico: [phone]