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Statistician CRO oversight
Technogarden AB
Technogarden är ett ledande konsultföretag som erbjuder uthyrning och rekrytering av ingenjörer, chefer och tekniska specialister, inom industri, energi, olja och gas, bygg och fastighet, infrastruktur, telekommunikation, IT och life science.
Vi har dedikerade kompetensområden inom projektledning, projektstyrning och telekommunikation.
Varje år genomför vi cirka 600 uppdrag i Norge och Sverige.
Med bred teknisk kompetens och lokal närvaro har vi i över 20 år varit en pålitlig samarbetspartner för både privat och offentlig sektor.
Vi levererar lösningar som ger våra kunder rätt kompetens och kapacitet – precis när de behöver det.
Som en del av Norconsult, ett av Nordens ledande konsultföretag, är vår spetskompetens förankrad i en större kunskapsmiljö.
Drivna av vårt gemensamma syfte – Varje dag förbättrar vi vardagen – skapar vi långsiktiga värden och samhällsnyttiga lösningar.
Life Science department within Technogarden is now looking for a skilled Statistician for an assignment on-site part time in Scania! We are looking for a statistician with fairly long experience who also can program in SAS and who can work for us about 50% for at least one year.
The assignment is on site, at our clients HQ in Lund.
It is of importance that you have excellent cooperation skills and like working in a biometrics team and also participate in inhouse trial team as the inhouse trial statistician together with different functions.
If you appreciate:
- High speed at work and the upper management is very involved, and may ask direct questions meeting with stat.
- High flexibility and confidentiality
- Important to keep deadlines
Your responsibilities:
- Oversight of CROs Stat/prog activities
- Give input to relevant section in the Clinical Trial Protocol and approve/sign off
- Lead or write SAP for a trial and for other non-study analysis of data and sign off
- Give input to relevant biometrics documents
- Lead and review shells and dry-run TFLs from CROs
- QC of program, if required
- Review and approve Clinical Trial Reports
- Give input to clinical programs, study designs and sample size calculation
- Perform statistical analyses, tables e t c on clinical data
- Keep up-to-date with statistical methodology relevant to the pharmaceutical industry and share knowledge
- Participate in regulatory meetings with authorities, if required
Candidate profile:
- University degree in statistics
- Experience within Statistics in the pharmaceutical industry and at a clinical CRO
- Experience in sas-programming
- Experience in CDISC
- Excellent communication skills
- Fluent in written and spoken English
Technogarden offers interesting assignments and we are a well established company where you will belong to a tight, inspiring team both within Technogarden and at our client! We need you urgently and look forward to our first discussion to see if this is a match for you! Don´t hesitate to contact us for further questions and information.