About Cannaflos and the position:

Cannaflos is an innovative pharmaceutical startup focused on the research and development of cannabis-based compounds and medicines. With a clear focus on scientific excellence and compliance, Cannaflos is driving the medical potential of cannabis, from plant to patient.

We are currently seeking a Project Manager Clinical Development to join our dynamic team. In this role, you will have the unique opportunity to work with cannabinoids and make a real difference in the lives of pain patients. As a key member of our clinical development team, you will oversee and manage clinical trials, ensuring they are conducted with the highest standards of scientific rigour and regulatory compliance. If you are passionate about advancing medical research and improving patient outcomes, we would love to hear from you.

Your new responsibilities:

Clinical Trial Management:

The role involves developing project plans, managing clinical trials from start to finish, and leading project team meetings.

• Regulatory and Compliance: The job requires ensuring that all clinical trials comply with regulatory requirements and company SOPs. It also involves preparing and submitting regulatory documents.
• Vendor and Site Management: The role includes identifying and managing relationships with CROs, clinical sites, and other vendors. It also involves overseeing site selection, initiation, monitoring, and close-out activities.
• Budget and Resource Management: The job involves developing and managing project budgets, monitoring project expenditures, and providing financial updates to senior management.
• Risk Management and Problem-Solving: The role requires identifying potential project risks and developing mitigation strategies. It also involves resolving project-related issues and challenges.
• Data Management and Analysis: The job requires ensuring data integrity and quality, overseeing the design and approval of Case Report Forms, maintaining trial documentation, and reviewing and interpreting clinical data.
• Stakeholder Communication: The role involves maintaining clear communication with internal and external stakeholders and preparing and delivering project updates, presentations, and reports.
• Team Leadership and Development: The job requires providing leadership and mentorship to project team members and supporting their professional development.

Your skills:

• Master’s degree in a life sciences field (e.g., biology, chemistry, pharmacology) or medicine; advanced degree (e.g. PhD, MBA) preferred.
• Relevant experience in clinical research and project management within the biotech or pharmaceutical industry or within a CRO.
• In-depth knowledge of clinical trial design, execution, and regulatory requirements (FDA, EMA, ICH-GCP).
• Proven track record of successfully managing clinical projects.
• Knowledge of biostatistics, data interpretation as well as critical design aspects of clinical trials.
• Very good oral and written communication in english.
• Excellent organizational, communication, and interpersonal skills.
• Strong problem-solving abilities and attention to detail.
• Proficiency in project management tools and software (e.g., MS Project, Smartsheet).
• Ability to work independently and as part of a cross-functional team.

We offer:

• A diverse and dynamic team
• Option for full home office work (except for travel) and flexible working hours
• Individual development opportunities and further training
• Have a significant voice in shaping company strategy
• Enjoy fast growth and promotion opportunities
• 30 days paid vacation
• Home Office Equipment
• Train Ticket for Germany (if applicable)
• Employee Participation

Further information:

This position is a fully remote working model. It is possible that your induction will take place on site in Cologne and/or Berlin. If it is not possible to be on site, a virtual induction is also doable.

You can send us your application via this platform or by e-mail to: clinicalmanagerjob@cannaflos.de. Your HR contact is Dominique Reinhard.

Stay up to date and connect with us on LinkedIn, where we regularly share updates on career opportunities, company developments and other exciting topics. At Cannaflos, we are committed to diversity and inclusion in the workplace and invite people from all walks of life to join our team.

You can find more information about our team and what we do here: www.cannaflos.de

Art der Stelle: Vollzeit

Gehalt: ab 45.000,00€ pro Jahr

Bewerbungsfrage(n):

• Do you obtain a Master’s degree in a life sciences field?
• Did you manage a clinical trial before?
• Do you have knowledge of biostatistics and data interpretation?

Arbeitsort: Zum Teil im Homeoffice in 50827 Köln

Voraussichtliches Einstiegsdatum: 03.02.2025