Medical Writer/Project Manager Wanted at Lihme Research & Healthcare

Lihme Research & Healthcare AB

Uppsala län, Uppsala

Previous experience is desired

22 days left
to apply for the job

We are expanding our operations and looking for an experienced and dedicated Medical Writer/Project Manager to join our team.

As a Medical Writer/Project Manager with us, you will be responsible for project management within Real World Evidence (RWE) studies and producing clear and accurate scientific documents that meet regulatory standards and client requirements. You will work closely with project managers, researchers, statisticians, and other partners.

About us

Lihme Research & Healthcare offers services in clinical research. We provide expertise in project management, study coordination, management of regulatory documents related to studies, training, and quality monitoring (monitoring and validation). Our clients include pharmaceutical companies, researchers, universities, and regions.

If you thrive on variety, take responsibility, and appreciate working in a smaller organization with short decision-making paths, then you have a chance to help develop our work in Medical Writing.

Our office is located in Kungsporten on Kungsängsvägen in Uppsala.

Your responsibilities

  • Create and process documents such as study protocols and clinical study reports in accordance with GCP and applicable standards.
  • Coordinate the development of these documents both internally and with clients.
  • Format scientific publications such as manuscripts, abstracts, and posters.
  • Project manage registry studies and data collection in studies.
  • Collaborate with cross-functional teams to gather and compile information from various sources.
  • Contribute to project management and scheduling to ensure timely deliveries.

We are looking for someone who:

  • Has an academic degree in medicine, nursing, pharmacology, biomedicine, or equivalent.
  • Has at least 2–3 years of experience as a Medical Writer or in a related field.
  • Has experience writing regulatory documents and/or scientific publications.
  • Is proficient in Swedish and English at a high level, both spoken and written.
  • Is meticulous, structured, and has strong analytical skills.
  • Can work independently and in teams and manage multiple projects simultaneously.
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