Starting a new role as a freelance CRA. Open to all CRA/clinical trial related tasks. Part time jobs are very welcome. Long or short term contracts will be considered.

Head of department performing clinical trials. Since 2010 also Head of Clinical Trials in Finland and now for the whole Nordic.Responsible for ensuring an efficient clinical research organisation and for securing quality improvement of the study processes and procedures.Manage and oversee team activities and report to Management team.Support team members to improve efficiency and increase quality.Maintain an agreed level of productivity - this has increased during the recent 3 years.Supervise study performance and advice and lead project managers and CRA's.Allocate adequate resources to deliver agreed commitment in global studies and also hire and co-operate with CRO personnel.Negotiating and contracting with CRO company.Preparing and supervising of personal development plans plus objective setting for all staff.Perform follow up of performance, productivity and objectives - either F2F or virtually.Handling of Performance Mangement on a daily basis.Train and mentor junior staff.Perform accompanied site visits and give feedback on communication and performance.From several restructures broard experience with change management - have been able to retain all personnel and to keep the productivity and spirit during hard times of uncertainty.Daily lead of 11 CRA's and formerly also 3 Study Assistants and 3 project leaders and member of the Nordic Leadership Team within Clinical Operations.

Responsible for performing clinical trials within different therapeutic areas.Site selection and negotiating/contracting with sites.Prepare/create and handle study related documents.Plan and perform pre-study, initiation, monitoring and closeout visits.Perform SDV and report AE's and SAE's according to SOP's and regulations.Create and maintain site file/ISF.Study drug handling - tracking and destruction.Forecast study timelines, resources, recruitment, budget, study material and study drugs.Create and maintain/update contingency plans for each site.Applications for EC and reporting of study progress.Train, support and advice investigators and other personnel in study related matters.Plan and perform national investigator meetings.GCP training for site personnel.Prepare for activities assosiated with audits and inspections.Training and mentoring of new CRA's.Keep track on research intelligence in local market.

Plan and perform sales visits.Participate in preparing promotion materials.Responsible for making a patient video regarding angina pectoris.Plan and complete sales/promotion meetings with GP's, specialists and pharmacy personnel.Preparing monthly/yearly plans for the district and sales.Mentoring and training of new sales personnel.Proud to be a member of the best selling team in DK.Responsible for several successful launches in the district.

Sales rep working with GP's and pharmacies. Mainly within the CV area plus OTC.Plan and perform visits to GP's and hospital specialists.Plan and perform trainings for pharmacy personnel.Promote a totally new concept within the treatment of Angina Pectoris.Plan and lead evening meetings for relevant personnel.Plan and perform pharmacy initiatives towards costumers.Part of a group creating sales promotion material.Responsible for sales within the northern district in DK and monthly reporting to headquarter.Proven sales increase in the district within OTC and CV area.