Culture and Careers.

About Teitur Trophics

Teitur Trophicsis looking to fill a hybridrole as ProjectManager/Clinical Trial Managerbased in our office in Aarhus,Denmark. This is initially a contract position until the end of 2026 with thepotential to turn into a full-time role in 2027. Teitur Trophics is a biotechcompany that develops first-in-class cyclic peptides in a number of therapeuticareas including neurodegenerative diseases where our lead asset is currentlyprogressing in the clinic for Parkinson’s Disease. The science behind TeiturTrophics involves decades of researchat Aarhus University on the Vps10p-domain receptor family membersSorCS1, SorCS2 and SorCS3.

The Role

The successfulapplicant will become a key member of the Preclinical and Clinical Developmentteam based in Aarhus, supporting the progress of our lead program into a PhaseII clinical trial in 2026/2027. Furthermore, the applicant will also beresponsible for the project management of the Teitur Quality Management System.The position reports directly to the CDO and the individual would be workingvery closely with experienced consultants in preclinical development, clinicaloperations and quality assurance. We are looking for an individual who has hadexposure to clinical trial management and understands the requirements ofpreclinical development. The individual will support the planning,communications and operational support of upcoming clinical trials outsourcedto external partners as well as taking on a project management type role to support preclinical development. The individual will also be part of the team supporting the preparation ofregulatory submission documents and overall quality assurance.

Whilst it isnot essential that the candidate is experienced in all aspects of this diverserole, a willingness to learn anddevelop will be key. The role requires good organizational and communicationsskills. Being a small biotech,the expectation is for each employee to get involvedin a number of differentaspects which also provides aunique opportunity for the right candidate to really grow and develop in thisrole.

Key Responsibilities

·    Project management of preclinical and clinical studies,create and evolvethe project development plan and assess critical pathactivities.

·    Key point-of-contactwith external partnerorganizations to ensurebudgets, contracts, resources,data quality and adherence to timelines are met.

·    Oversight of the Phase Iand Phase II clinical trial set-up and management, workingclosely with the CDO,CMO and Clinical Operations consultant to ensure the trial is conducted toappropriate corporate and regulatory standards.

·    Oversight and projectmanagement of the Quality Management System, working closely with the CDO andthe Quality Assurance consultant to ensure that the company is operating at theappropriate level of compliance.  

·    Effectively communicate projectprogress updates with the management team, highlight potential delays,mitigations and action plans, escalating any performance and quality issues.

Desired skills and experience

·        A degree in Life Sciences or a relatedfield.

·        Project management experience in a biotech/pharma environment or healthrelated field.

·        Background in clinical researchand/or preclinical development.

·        Experience in working with external partnersand coordinating complexprojects with multi-site input.

·        Excellent communication skills and attentionto detail.

·        Self-motivated, able to work independently and have an active interestin drug development.

‍

Application & info

Deadline for application: March 20^th 2026 (however shoulda suitable candidatebe identified beforethe deadline, the job application will be removed)

Role is based in our Aarhus office, but a hybridposition could be considered.

Start Date:Immediately or June 2026 at the latest

Send cover letter and CV in English marked“Project Manager/Clinical Study Manager” to info@teiturtrophics.com.

‍