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Senior Trial Manager

Remote: 
Full Remote
Experience: 
Senior (5-10 years)
Work from: 

Offer summary

Qualifications:

Strong knowledge of GCP regulations, 6 years' clinical trial management experience, Experience with study start-up and closeout, DEC/IRB applications.

Key responsabilities:

  • Lead and manage CTIMP and non-CTIMP trial programs
  • Coordinate project partners and oversee project progress
  • Facilitate team training; collaborate with tech and product teams
  • Contribute to clinical strategy and business development
  • Support inspection readiness and develop risk mitigation strategies
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Lindus Health Research TPE https://www.lindushealth.com/
11 - 50 Employees
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Job description

🍊Our mission

All new medicines need to undergo clinical trials to show they’re safe and effective. But today’s clinical trial infrastructure is stuck in the past, and the cost of developing new medicines has skyrocketed as a result. Patients have to wait longer and pay more for new treatments. 

Our mission is to fix this; we use software to help innovative companies run faster, more reliable, and patient-friendly clinical trials. We’re still a young company, but we’ve already had a big impact. Since founding the company in March 2021 we’ve helped run over 80 clinical trials involving tens of thousands of patients. 

In August 2023 we raised an $18m Series A round from some of the world’s top investors including Creandum, Peter Thiel, Firstminute and Seedcamp to power the next stage of our growth. 

🍊About you

We'd like to hear from you if...

  • You bring strong knowledge of Good Clinical Practice/ICH guidelines, regulatory requirements, drug development process and clinical monitoring procedures

  • You have >6 years' experience managing and co-ordinating clinical trials in a project management and/or clinical operations role

  • You're experienced in leading and line-managing a team

  • You have experience with study start-up, closeout and EC/IRB applications

  • You have experience using different software for delivery of clinical trials and are able to adapt to using new technology to change the way trial processes are delivered

  • You've worked on decentralised/remote trials

  • You've run multi-site and IND/CTIMP trials

  • Previous startup/biotech experience is a plus
    ‍

🍊What you'll focus on

Project Leadership and Delivery:

  • Lead and manage the day to day running of CTIMP and non-CTIMP clinical trial programs and projects,  ensuring that they delivery successfully (i.e., conduct trials on time, on budget, in compliance, and of high quality)

  • Acts as primary liaison between Lindus Health and the Sponsor to ensure project launch, conduct, and closeout according to the Sponsor’s and Lindus health's contractual agreement

  • Coordinates activities and deliverables of all project partners and proactively identifies and manages issues

Reporting and Communication:

  • Accountable for maintenance of project information on a variety of databases and systems

  • Maintains and evaluates project progress by maintaining timelines and other tracking/analysis tools

  • Responsible for project management components of inspection readiness for all aspects of the project conduct, including Trial Master Files

  • Provides oversight for development and implementation of project plans in accordance with Lindus Health standard operating procedures

  • Directs the activities of assigned Project Support staff and mentors other project management team members and clinical staff; facilitates team building and communication

  • Develops contingency planning and risk mitigation strategies to ensure successful delivery of project goals

Training:

  • Facilitates team training in accordance with protocol and/or project requirements, including therapeutic, protocol specific, and process training

Collaboration:

  • Work closely with the tech and product teams to help design best-in-class trial technology that exceeds customer demands (e.g., EDC, e-Consent, eTMF)

  • Collaborate with Quality Management to develop formal study requirements that enable rigorous validation of clinical trial software, and contribute to the development and maintenance of our standard operating procedures and policies

  • Contribute to our clinical strategy as an early employee of the clinical operations team

Business development:

Support business development work with Sponsors and vendors where necessary

🍊What we offer

  • Have an impact across all areas of our business and fix one of the world’s most broken industries 

  • Competitive salary, plus meaningful stock options

  • Unlimited holidays; everyone is encouraged to take off at least 28 days each year

  • Enhanced Parental Leave- 12 weeks full pay for primary care giver & 4 weeks full pay for secondary care giver

  • Gympass membership; flexible access to gyms, studios, classes and wellness apps

  • Expense your lunch 1 day per week

  • Company away days - this year we went to Nashville!

  • Up to $2000 per year towards courses and development

  • A new laptop as your main workstation and up to $1000 towards setting up your home office

🍊Our hiring process

  • Initial conversation with George (Director, Talent) (30mins)

  • Second meeting with our ClinOps team (30 mins)

  • Functional Interview with 2 members of the ClinOps team (45 mins)

  • Values interview with 2-3 members of our Founding team (30 mins)

Required profile

Experience

Level of experience: Senior (5-10 years)
Industry :
Research
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Motivational Skills
  • Verbal Communication Skills
  • Adaptability
  • Team Management
  • Collaboration
  • Leadership Development

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