Clinical Project Manager

WORKING AT MÖLNLYCKE
Are you looking for a great career and want to make your mark? Could you help improve healthcare outcomes around the world? If the answer is yes, you think just like us and should make your next move in your caarer and apply for this exciting opportunity that we have below.
We are looking for a Clinical Project Manager to join our journey. As our new team member you will be responsible for the executioin of global clinical projects according to applicable guidelines/laws, timelines budgets and quality standards.
You will be working with projects from start to finish, where you have the possibility to improve and develop the future. You will build and maintain organizational relationships. To be successful in this role you need to have strong negotiations and communications skills to work with different stakeholders.
We are looking for someone with a solution-orientated mindset and strong work ethic. We want our new team member to have a strong feeling for ownership and autonomy. You will be accurate and have a creative way of thinking which makes you stand out. The role is based in HQ in Gothenburg, Sweden.
Key Accountabilities
Being part of cross functional teams and global teams to lead clinical projects.
Developing Clinical Investigation Plans with focus on practical feasibility (design, time plan, country/site/investigator selection, budget).
Developing Clinical Investigation Reports, including contributing in the analysis of clinical data.
Compliant execution of clinical investigations.
Timely management of all operational aspects of assigned clinical investigations (e.g. CRO/site/lab selection, milestone delivery, enrolment, data consistency, investigation products).
Contract management (negotiation, management, payments) and documentation.
Submissions to competent authorities and ethics committees.
Vendor and site management (e.g. selection, training, monitoring, follow-up).
Ensures regular and timely progress reporting (milestones, budget, timelines).
Review and update of applicable SOPs.
Perform/supervise/coordinate site visits such as site selection, initiation, training, management, monitoring, close out.
Oversee data management activities throughout the study.

Your Qualifications
Relevant (Life science) education on MSc level.
Minimum 3 years of experience in Clinical Project/Study Management (preferably Medical Device) in an international setting.
Proven track record of working in cross functional teams.
Solid experience of managing various study types in different phases eg. pre/post-registration study involving patients, healthy volunteers, and/or registries.
Relevant knowledge of GCP and applicable regulations/laws.
Basic understanding in statistics, data management and scientific writing.
Fluent in English (written and spoken).

We will evaluate candidates continuously, don’t hesitate to send us your application. We will contact only selected candidates.
We look forward hearing from you.