TIKOMED is looking for an experienced Project Leader
We are looking for you who are passionate, skilled and with strong track record and high personal commitment. You want to contribute and be part of our exciting journey in the creation of novel therapies for severe diseases.
TIKOMED is a biopharmaceutical company developing ground breaking projects in neurology and ophthalmology. ILB is our exciting new pleiotropic molecule with the potential to treat several neurological diseases and the cause of glaucoma. First into clinic is our treatment for ALS (Amyotrophic Lateral Sclerosis) to be followed by a glaucoma study. In parallel we are also developing our IBsolvMIR drug which helps cells survive attacks from the innate immune system.
We would like for you to focus on our forthcoming Phase II program for ILB, where additional indications are currently being evaluated.
We are located in the countryside outside the village of Viken not far from Helsingborg. We also have a research site in Uppsala Science park. As of today, we are 5 employees but plan to add colleagues to our team. We aim to attract and collaborate with the sharpest minds over the world to keep our science exciting.
The work consists mainly of project management and project administration with regards to:
• Planning and structuring clinical studies.
• Coordinate with our ILB Executive and investigators.
• Lead and maintain contacts with external partners (CRO, University, etc.) and compile documentation in a regulatory correct manner in preparation for interactions with both Swedish and international authorities.
• Gather knowledge and competence in the main clinical and research fields, carry out literature studies and write study applications, manuals, minutes and summaries.
• Create basic schedules and budget.
Project work is a team effort where your role is to lead and co-ordinate the network of both internal and external skills and capabilities to optimize our results. You work independently, and have the ability to make your own priorities, shifting focus between the company’s various projects.
You are positive, problem solving, self-perpetual and goal oriented. You have extensive experience in project management of clinical trials and regulatory affairs.
Your educational background is in natural science, at least equivalent of the Master level, preferably in the pharmacology, biology or biomedicine. Experience from work in the industry / authority / consultancy about production / quality issues, regulatory work and / or clinical trials is a requirement. You express yourself in English fluently both in written and oral terms. You have all necessary computer skills and can handle all common MS Office programs as well as Share Point, general software and cloud-based programs.
Send your application by e-mail, no later than 24 August to TikoMed AB, firstname.lastname@example.org or TIKOMED AB, Box 81, 263 03 Viken.
For further information, please contact: CEO, Anders Kristensson: Tel: +46 734-32 32 45
E-mail email@example.com. or visit www.tikomed.com