Medicorent is a Scandinavian Contract Research Organization providing innovative full-service solutions to the local startups and pharma industry in the Nordics and some European countries through collaborators. Our clients and partners include pharmaceutical, biotechnology, medical device, bio-pharmaceutical and food supplement companies. With a close network of over 100 active consultants and access to a great number of candidates in the life-science area, we take care of our internal projects as well as being able to offer long- and short term resourcing solutions to our clients with a firm commitment to quality and cost effectiveness to help clients and partners bend the cost and time curve of drug development and life cycle management to deliver life-changing therapies and improve health and well-being of us all as we are all patients, sooner or later.
We have a new opening for a Clinical Team Manager / Project Manager for our operations. This is a permanent position and can be office/home-based in Stockholm and will be assigned to both external and internal projects.
Planning, execution and delivery of Clinical Trials, including participation in cross-functional planning sub-teams of the Sponsor.
Act as Clinical Outsourcing Manager for our clients by coordinating the process for identification, selection and contracting of suppliers/freelancers.
Lead and coordinate clinical trials (together with partners and other external service providers) to ensure quality, consistency, and integration of study data and progress operational deliverables to time, cost and quality objectives from start through close-out activities.
Assist in the development of protocol, case report form and other study documents.
Ensure that clinical trials are executed according to protocol, Standard Operating Procedures (SOPs), ICH GCP Guideline and regulatory requirements.
Qualifications and Experience:
University degree in a science related field
Minimum of 10 years’ experience of conducting clinical trials from the pharmaceutical/biotech/CRO industry
Experience of managing external service provider
Experience of clinical trial protocol and clinical documents writing
In depth knowledge of ICH-GCP as well as EU and FDA requirements
Effective communication, organizational, and problem-solving skills.
Leadership and teambuilding skills
Excellent Swedish and English skills. Language skills in German is advantageous.
Your hard work will be rewarded with a competitive base salary, as well as a benefits package including 30 days’ vacation per year, pension scheme as well as other leading-edge benefits that you would expect with a company of this type.
Apply today! For more information about the position, you are welcome to contact Nicole H´Lyon, Recruitment Manager, at email@example.com
Applications are processed on an ongoing basis. We look forward to hearing from you! Please note that we cannot accept applications via email due to GDPR.
Our goal is to build long-term relationships with our candidates, employees and customers. We are a flexible organisation with genuine interest in people and the willingness to see the individual behind the CV. We create opportunities together as a team and empower our employees to be part of our journey towards becoming the number one Scandinavia company providing full scale CRO. As a candidate, we will follow your progress in your career for years to come and we are committed to offer career development in accordance to your own preferences.