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Clinical Research Scientist Chase

Barrington James

Milano

Ibrido

EUR 60.000 - 90.000

Tempo pieno

8 giorni fa

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Descrizione del lavoro

A leading biotechnology company is seeking a Clinical Project Manager specializing in CNS. The role involves overseeing clinical trials, ensuring regulatory compliance, and managing resources effectively. Candidates should have significant experience in project management within CNS, fluency in English and Italian, and strong leadership skills.

Servizi

Competitive salary and benefits
Performance-based incentives
Opportunity for personal growth
Collaborative culture fostering innovation

Competenze

  • 5 years in clinical trial/project management, especially in CNS.
  • Proficiency in project management tools and systems.
  • Fluent in English and Italian.

Mansioni

  • Manage all phases of CNS clinical trials simultaneously.
  • Ensure compliance with regulatory guidelines and manage budgets.
  • Lead site management and data collection processes.

Conoscenze

Leadership
Project Management
Communication

Formazione

Bachelors or advanced degree in life sciences

Strumenti

Project Management Tools

Descrizione del lavoro

Job Description : CNS Clinical Project Manager

Position : Clinical Project Manager CNS

Employment Type : FullTime

Industry : Biotechnology

Company Overview :

Join a wellestablished and fully funded biotech company at the forefront of central nervous system (CNS) therapeutics. With an innovative pipeline targeting unmet medical needs in neurology and psychiatry we are expanding our clinical operations team and are seeking a dedicated Clinical Project Manager (CPM) to oversee and drive our CNS clinical trials to success.

Key Responsibilities :

Clinical Trial Oversight :

Plan execute and manage all phases of CNS clinical trials ensuring they are delivered on time within scope and budget.

  • Oversee multiple trials simultaneously across international sites ensuring alignment with company objectives.

Collaborate with crossfunctional teams including regulatory data management medical affairs and external vendors.

  • Act as the primary point of contact between sponsors investigators and site staff to ensure effective communication.

Regulatory & Compliance :

Ensure all trials adhere to ICHGCP guidelines company SOPs and relevant regulatory requirements.

  • Prepare and review essential regulatory documents and submissions to ethics committees and authorities.

Budget & Resource Management :

Develop track and manage clinical trial budgets contracts and resources.

  • Optimize resources to meet trial objectives efficiently.

Vendor and CRO Management :

Select contract and oversee thirdparty vendors including CROs ensuring quality deliverables and adherence to timelines.

  • Conduct regular performance reviews and risk assessments to maintain vendor accountability.

Site Management :

Lead site identification initiation and monitoring to ensure highquality trial conduct.

  • Address site challenges proactively and implement corrective actions as needed.

Data Integrity and Reporting :

Ensure robust data collection monitoring and quality control processes.

  • Collaborate with biostatistics and data management teams for timely data analysis and reporting.

Required Qualifications :

  • Education : Bachelors or advanced degree in life sciences pharmacy or a related field.
  • Experience :

5 years in clinical trial / project management with a strong focus on CNS therapeutic areas.

  • Proven track record of managing international multisite trials.
  • Handson experience with all phases of clinical trials especially Phase IIII.
  • Skills :

Deep understanding of CNS disorders and their clinical development challenges.

  • Strong organizational leadership and decisionmaking abilities.
  • Proficiency in project management tools and systems.
  • Fluent in English and Italian (both written and verbal).

Preferred Qualifications :

  • Prior experience in biotech or pharmaceutical CNS drug development.
  • Knowledge of emerging CNS therapies biomarkers or advanced trial designs.
  • Familiarity with Milans clinical research ecosystem and key opinion leaders.

What We Offer :

  • An opportunity to work with a highly skilled and passionate team in a cuttingedge biotech environment.
  • Competitive salary benefits and performancebased incentives.
  • A collaborative culture fostering innovation and personal growth.
  • The chance to contribute to lifechanging therapies for CNS disorders

hybrid

italy

LILC1

Key Skills

Laboratory Experience,Machine Learning,Python,AI,Bioinformatics,C / C++,R,Biochemistry,Research Experience,Natural Language Processing,Deep Learning,Molecular Biology

Experience : years

Vacancy : 1

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