Anna Westerdahl Email & Phone Number

Stockholm, Stockholm County, Se

Stockholm, Se

Stockholm, Se

Lund, Skåne, Se

Lund, Skåne, Se

Huddinge, Se

Lund, Skåne, Se

Lund, Skåne, Se

Coordinating and managing CRAs in a global trial. Aid to project management. Creation and writing of necessary manuals and instructions. Overall tracking of study specific activities.

Lund, Skåne, Se

Overall responsibility for project delivery in a global trial.

Lund, Skåne, Se

TFS is a comprehensive full-service Contract Research Organisation (CRO) dedicated to assisting our clients in the development of their new drugs. Offering the highest level of competence and experience, TFS is all about people; people you can trust to deliver the highest level of competence, experience and personal attention to your clinical trials.We will support every aspect of your clinical trial in all clinical phases and all clinical disciplines.For more details visit www.tfscro.comCurrently Lead CRA in global trial.*Monitoring report review*Main contact for and support to country CRA:s*Link between CRA:s and Project Manager*Experience as application specialist*Start-up, conduct and closing of clinical trials*All phases except phase I*IP-managment*Contracts*Indications; oncology, pain, diabetes, vaccines and renal disease*Oracle based CRF, electronic archiving*Good language skills

Brentford, Middlesex, Gb

Help to CRA:s during start-up phase. Applications to MPA, ethics committee, biobank committee, radiology board and data protection board. Submission of amendments during the conduct phase and all tasks (up-date of ICF etc.) that comes along with an amendment. Also support to the vaccine team.

New York, New York, Us

Pre-study activities, start-up and conduct of clinical trials. Applications to ethics committee and MPA during the end of the contract placement.

Working with in-house projects or out-sourced to client depending on what's requested. All different phases of clinical trials except for Phase I. From feasibility to close-out. Leading projects within compliance and adherence. I also planned and conducted feasibility studies within adherence. I also made a smaller market survey to investigate the CRO market within a few Asian countries during my time at Adxto.

New York, New York, Us

At Pfizer I was lead CRA for three studies; one compassionate use study, one Phase III renal oncology study and one Phase II women's health study. The work included planing and preparing monitoring activities, conducting and reporting monitoring visits as well as IP-management and filing. I also started an oncology study on Prostate cancer before the assignment ended. I prepared and conducted the initiation visits and the contracts negotiations together with the feasibility specialist.

Contract placement with clients. Part of my time at IRW Consulting I was contract placed with a client as a Clinical Trial Assistant learning the entire process of the clinical trial from the bottom. I moved on to a CRA position after ½ a year and became responsible CRA for three different trials within different therapeutic areas.

Paris, France, Fr

During my time at sanofi-aventis as contract place clinical trial assistant I was responsible for the study files together with the CRA. I also had the main responsibility for the economy and worked closely with the project manager. I helped compile ethichs applications and took part in the planning of investigator's meetings among other things.

Cambridge, Cambridgeshire, Gb

Pre-clinical toxicity studies at the safety assessment department. Working mainly with bone marrow toxicities and toxicities affecting the blood. This was a fixed-term employment.

1 Y Pre-Doctorial Studies, Medical Research

Master Of Science (M.S.), Medical Biology

Master Thesis, Medical Research