Ansök senast2026/02/25
PlaceringLund
Anställande företagCamurus AB

CAMURUS AB

PATIENT SAFETY MANAGERS

Camurus is a Swedish research-based pharmaceutical company committed to developing and commercializing innovative and long-acting medicines for the treatment of severe and chronic conditions, including opioid dependence, pain, cancer and endocrine disorders. New drug products are based on our proprietary FluidCrystal ® drug delivery technologies with the purpose to deliver improved quality of life, treatment outcomes and resource utilization. The company’s share is listed on Nasdaq Stockholm under the ticker “CAMX”. For more information, visit camurus.com.

We are strengthening our global Patient Safety team at the headquarters in Lund by recruiting Patient Safety Managers. We are both looking for experienced candidates with good understanding of safety databases, case processing, and project management experience, and more junior Patient Safety candidates.

You will work with committed colleagues with both post-marketing and development projects. Camurus is a rapidly growing and innovative company, and you will have a strong impact on the activities in the development of the Safety database.

You will report to the Director of Patient Safety.

The role:

As Patient Safety Manager, you are committed to ensure patients’ safety and product quality across the Camurus products. In this role, you will be involved in the development and maintenance of our global safety database. You will play a key role in ensuring a reliable, compliant, sustainable, and cost-effective supply of high-quality maintenance and development activities.

You will first and foremost ensure a compliant Pharmacovigilance System for safety surveillance for Camurus products. You will also support digital surveillance by using data driven methods and approaches.

Among others, your responsibilities will include:

  • Conduct and drive the digitalisation, automatization, and surveillance activities of safety systems and databases and its life cycle management in accordance with applicable legislation

  • Drive and lead internal cross-functional teams (Safety, IT Quality, etc.) for safety database projects and activities

  • Ensure alignment of supplier qualifications, audits, and ongoing performance monitoring activities with the overall strategic activity plan

  • Ensure adherence to company policies, industry standards, and applicable regulations (FDA, EMA, ICH)

  • Establish, develop, and maintain strong relationships with key and strategic collaboration with several departments internally to ensure continuous improvement and efficiency, quality, of the safety database and compliance of the activities

  • Perform review and quality control of ICSRs/SAE and ensure timely submission and exchange of these

  • Develop the quality system in the area of expertise, as per GVP requirement

  • Support the QPPV to enable the QPPV to maintain oversight of the Safety database

Candidate profile:

We are looking for candidates with experience within Drug- or Patient Safety/Pharmacovigilance from the pharmaceutical/medical device industry. You probably have a background as a pharmacist, nurse or an education within pharmacology or pharmaceutical science.

We think the below is part of your experience:

  • ICSR/SAE processing, signal detection, aggregate report compilation, and clinical trials

  • Case processing in safety databases

  • Database administration of one or more Pharmacovigilance databases

  • Cross-functional IT projects

  • Quality processes regarding Change Control and Good Documentation Practice

  • GVP, regulatory compliance, and quality

  • Safety database administration

You are self-driven, attentive to details, with a proven ability to deliver results in a fast-paced organization. Ownership and a pragmatic mindset are some of your key characteristics. To be successful in this role you are collaborative and solution oriented. You possess strong business acumen together with excellent communication and stakeholder management skills.

Camurus offers:

This is a great time to join a highly dynamic company during a very exciting phase of growth. The position offers an international work environment and corporate culture, with the possibility for individual development and growth. The corporate culture is driven by our core values of innovation, collaboration, ownership, quality, and passion for realizing our patient-centric commitment.

Application:

This is an immediate, full-time employment opportunity. The application process is ongoing, so apply with your cv and cover letter as soon as possible, at the latest 25th of February 2026. Please note that we do not accept applications by e-mail.

Read more about how Camurus will process your personal data here.

We are looking forward to seeing your application!

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