Team Lead Clinical Trial Management (w/m/d) @ Hamilton

Domat, GR
Vollzeit
26.11.2024
Vollzeit
Lionstep AG

Team Lead Clinical Trial Management (w/m/d) @ Hamilton

Stellenbeschreibung

We work directly on behalf of Hamilton and do not charge any agency fees.


What this position has to offer:

Wide range of further training and development opportunities
  • Newly created position and the possibility of building your team
  • Familiar working environment, Home Office opportunity Own pension fund with a choice of three options


Interested? Then book a call with us now!


On behalf of Hamilton, we are searching for their next Team Lead Clinical Trial Management.

Job Summary


Would you like to take on new challenges? Do you want to work on innovative projects in a dynamic team? Then watch out!


As a recruiting partner of Hamilton we are looking for you as Team Lead Clinical Trial Management (a) 80 - 100 % at the location in Domat/Ems.

You can look forward to an incredible working environment, exciting projects and a motivating colleagues. You will also receive a wide range of training opportunities, leisure activities and other attractive benefits!

Have we piqued your interest? Then arrange an initial consultation with us now! ?

Depending on your qualifications and professional experience, this position offers a salary ranging from 120,000 to 130,000 CHF, including a variable component.

#Team #Leader #Clinical #Trial #Management #JoinTheTeam #JobOpportunity


What You Will Be Doing


Leadership and Team Management

  • Leading, mentoring and developing the clinical trial organization at Hamilton Medical, fostering a collaborative and high-performance culture
  • Providing guidance and support to team members on clinical trial processes, regulatory requirements and company policies
  • Conducting regular performance reviews and developing training plans for team members
  • Developing trial strategies and ensuring the successful execution of clinical studies from inception to completion

Clinical Trial Portfolio Oversight

  • Overseeing the planning, implementation, and management of clinical trial portfolio (mainly European and US trials), including protocol development, site selection, and patient recruitment

Developing and managing trial portfolio budget, timelines, and resources

  • Regulatory Compliance and Quality Assurance
  • Ensuring trials are conducted in alignment with our product innovation strategy, regulatory requirements, company SOPs and ethical standards in compliance with GCP, ISO 14155, MDR and other relevant regulations
  • Monitoring regulatory requirement updates
  • Liaising with regulatory authorities as needed
  • Developing and updating SOPs related to clinical trial management

Data Management and Reporting

  • Managing and developing the overall clinical data management: data collection, quality, and analysis processes to ensure data integrity and accuracy
  • Preparing regular progress reports for senior management and regulatory bodies
  • Ensuring timely and accurate reporting of adverse events and deviations

Stakeholder Communication

  • Serving as the primary point of contact for investigators, study sites, and external vendors (e.g. CROs)
  • Facilitating communication with other internal departments, including R&D, regulatory affairs, and clinical affairs
What You Bring To The Job
  • Master’s degree in life sciences, engineering or a related field
  • Multiple years of experience in clinical trial management within medical device industry, with at least 3-4 years in a leadership role
  • In-depth knowledge of GCP, ISO 14155, and regulatory requirements (MDR) for medical devices
  • Proven track record of managing clinical trials from initiation to completion
  • Track record of successful talent recruitment and development
  • People’s lead mentality, strong leadership, organizational, and communication skills
  • Motivation to act as an architect of an effective and efficient CTM organization, interpreting this task as a challenge and attractive opportunity
  • Ability to manage multiple projects and prioritize effectively
  • Proficiency in clinical trial management software and clinical data management


  • English: C1 – Advanced

Nice-to-Haves
  • Certification in clinical research, PhD and FDA experience are a plus
  • Ge: B2 – Upper Intermediate

Team
  • Reports to: Dominik Novotni - manager research and new technology
  • Colleagues: 5

Benefits
  • Work From Home (WFH) possible
  • Employee discount for many leisure activities & services
  • Green Sense: the healthy & sustainable staff restaurant
  • Events: Summer & Christmas party
  • Sports & fun
  • Counselling services with external partners for various life situations
  • Diverse training & development opportunities
  • Family-friendly employer
  • Five weeks of vacation
  • 13th monthly salary
  • 42.5 hour weeks in a flexitime model
  • Time off in advance for bridging days between Christmas & New Year
  • Own pension fund with a choice of three options
  • Continued payment of wages in the event of illness, accident & pregnancy
  • Compulsory health & accident insurance


Hamilton Company specializes in the development, manufacturing and customization of precision measurement devices, automated liquid handling workstations, and sample management systems. Hamilton's processes are optimized for quality and flexibility. Whether it's a custom needle with a quick delivery time frame, a special length pH sensor, or a comprehensive solution to fully automate your assay workflow, trust that Hamilton products will always meet your needs.

Hamilton Company has been a leading global manufacturer for more than 60 years, with headquarters in Reno, Nevada; Franklin, Massachusetts; Timi?oara, Romania; Bonaduz, Switzerland; and subsidiary offices throughout the world.

Job Types: Full-time, Part-time