Senior Clinical Data Manager

Employer
Medella Life
Location
Sweden (SE)
Salary
66,000 SEK per month
Closing date
10 Oct 2020

View more

Discipline
Data Management / Statistics, Clinical Data Management
Hours
Full Time
Contract Type
Permanent
You need to sign in or create an account to save a job.

Responsibilities

  • Provide Data Management deliverables in accordance with internal and external company requirements. 
  • Proactively coordinate and perform start-up, processing and finalization activities as detailed in our SOPs. 
  • Lead study setup including design, database structure, document creation; including approvals. 
  • Communicate with cross functional groups throughout the project lifecycle. 
  • Monitor project scope. 
  • Proactively manage project budgets, including time spent on data management tasks, and associated timelines and projections. 
  • Proactively manage project quality through supervision and quality control of team members’ work. 
  • Participation in reviewing and responding to QA audit reports. 
  • Proactive participation in appropriate sponsor/project team meetings. 
  • Conduct internal and external team meetings as necessary 
  • Provide training to site personnel in person or via electronic meetings 
  • Act as key data management contact for the project. 
  • Active involvement in departmental and organisational meetings and initiatives. 
  • Develops and documents departmental procedures. 
  • Participates in the review of cross functional department procedures. 
  • Training and Mentoring of team members in accordance with established departmental procedures. 
  • Represent our company at client meetings and bid defences. 
  • Oversee the project including leading the project team, communication with the client, ensuring adherence to timelines and budget responsibility. 

Requirements

  • College graduate with a degree in life science, computing or nursing qualifications preferred; or 3 to 4 years equivalent experience.
  • Minimum of 6 years of experience and/or demonstrated aptitude for data management work. International team experience preferred. 
  • Experience working in pharmaceutical and/or Contract Research Organization (CRO) industry preferred 
  • Prior trial responsibility for entire data management life-cycle 
  • Working knowledge of EDC studies 
  • Experience working in a home office environment, as applicable
  • Excellent organizational skills 
  • Strong written and verbal communication skills 
  • Exceptional attention to detail 

Company Profile

As specialist recruiters in life sciences, our mission is to create a positive impact in the world. We place visionary people in thriving cultures where they can create a brighter future. Our impact and what that means to society is why we go the extra mile. We even baked it into our name, Medella, which means to heal. Pairing brilliant scientists with brilliant companies we find wildly exciting, and it drives everything we do.  

​No matter how hard, at Medella Life we live by our values. We may be new, but we are here to earn our stripes. Our founding team has more than twenty-five years experience in the field. Our mission is to be your first call when looking for A-list talent. What matters to us is being the best, not being the biggest. That's why we value quality over quantity. It is our belief that science can save the world. Which is why a Medella Life is a good life.

Contact Us
  • 10 York Road
  • London
  • SE1 7ND
  • United Kingdom
  • +44 20 4511 0354
You need to sign in or create an account to save a job.

Get job alerts

Create a job alert and receive personalised job recommendations straight to your inbox.

Create alert