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Project Manager, Cardiac Safety (f/m/x)

extra holidays - extra parental leave
Remote: 
Full Remote
Contract: 
Experience: 
Mid-level (2-5 years)
Work from: 

Offer summary

Qualifications:

Bachelor’s degree or proven Project Management experience, 1-4 years of Project Management experience in pharmaceutical field, Knowledge of drug development process, Excellent organizational and time management skills, Working knowledge of Microsoft Office products.

Key responsabilities:

  • Direct and manage client project services ensuring quality and budget adherence
  • Lead study management phases including planning, monitoring, and closeout
  • Monitor timelines, budget reviews, and risk mitigation strategies
  • Manage internal/external negotiations and foster a collaborative team environment
  • Ensure compliance with training requirements and attend necessary meetings
Clario logo
Clario Biotech: Biology + Technology XLarge https://clario.com/
5001 - 10000 Employees
See more Clario offers

Job description

Clario, a renowned leader in cardiac safety with half a century of expertise, is seeking a talented Project Manager (f/m/x) to bolster our Cardiac Safety team in Hungary.
With a steadfast commitment to excellence, we centralize data collection using robust, responsive, and reliable tools, guaranteeing credible, compliant, and high-quality data. If you're passionate about making a difference in healthcare and thrive in dynamic environments, join us at Clario and be a part of shaping the future of clinical research.

What we offer

  • Competitive compensation

  • Attractive benefits (security, flexibility, support and well-being)

  • Engaging employee programs

  • Remote working

What you'll be doing

  • Responsible for directing and managing services for client projects to assure high quality, on-time, and on-budget services while promoting excellent customer service.

  • Lead the Planning and Setup, Monitoring, and Closeout phases of study management which includes:

  • Gathering customer requirements and relaying to internal teams

  • Developing study documentation

  • Distributing/tracking equipment

  • Creating/distributing reports

  • Archiving study data and documentation

  • Appropriate setting and fulfilling of customer expectations

  • Monitor study timelines and manage the financial components of each program/study, which includes:

  • Budget reviews

  • Revenue forecasting

  • Scope changes

  • Invoice reconciliation

  • Identify potential study risks and mitigations and escalate as appropriate

  • Manage internal/external negotiations and promote collaboration to foster a positive team environment, effective communications, and efficient use of resources to meet study timelines and contractual obligations

  • Apply problem solving strategies to address customer issues and maintain issue tracking documentation to monitor progress and ensure timely resolution to customer escalations

  • Ensure compliance with timely training completion/documentation.

  • Present study services at Investigator Meetings or site initiation meetings as needed.

  • Attend client meetings with Business Development and/or Operational teams to present Company services and Operational Data flow, as needed.

  • Assist with training new members of the Project Management team.

What we look for
  • Bachelor’s degree and/or proven Project Management skills or experience within the industry. 

  • 1- 4 years of experience in Project Management with an emphasis in the pharmaceutical field (or related industry experience). 

  • Knowledge of the drug development process.

  • Excellent organizational, interpersonal, time management, and prioritization skills.

  • Excellent verbal and written communication skills, including ability to communicate effectively in English.

  • Working knowledge of Microsoft Office products.

  • Detail oriented and demonstrated responsiveness to inquiries and requests.

At Clario, we put people first, always. We are united and driven by patients, committed to making a difference, and we are always looking for the best talent to help us transform lives. We value the contribution each of our people brings. It’s only through our people that we can continue to innovate technology that will shape the future of clinical trials.

#LI-NF1

Required profile

Experience

Level of experience: Mid-level (2-5 years)
Industry :
Biotech: Biology + Technology
Spoken language(s):
EnglishEnglish
Check out the description to know which languages are mandatory.

Other Skills

  • Social Skills
  • Time Management
  • Organizational Skills
  • Microsoft Office
  • Prioritization
  • Non-Verbal Communication
  • Customer Service
  • Problem Solving

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