Clinical trial manager phase I
Location: NetherlandsThe Company
My client is a clinical stage biopharmaceutical company that is conducting stage 1 clinical trials in gene therapy.Role Description
As the clinical trial manager you will be part of the clinical team that directly reports to the COO. You and your counterpart are responsible for two types of studies conducted in the Netherlands and in Canada. A new study site will be added to the portfolio that you will directly take over.The trials themselves are conducted by CRO's that you will need to manage in terms of results and logistics.
Some travel will be involved up to once a month for a couple of days.
Responsibilities
You will be responsible for the operational management and oversight of the trial at the new study site. You are responsible for managing the project, the external partners and logistics involved. You establish milestones, track and report study progress. You are responsible for good, clear and positive communications with external parties and study staff.Requirements
- MSc in biomedical sciences or similar- 5+ years of trial management experience with CRO management knowledge
- Hands-on mentality in study progress, troubleshooting and generally open to go the extra mile when called upon
- Fluent in English
- Strong personality with emphatic management style
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Naut van Osnabrugge.
Opis stanowiska
The Company
My client is a clinical stage biopharmaceutical company that is conducting stage 1 clinical trials in gene therapy.Role Description
As the clinical trial manager you will be part of the clinical team that directly reports to the COO. You and your counterpart are responsible for two types of studies conducted in the Netherlands and in Canada. A new study site will be added to the portfolio that you will directly take over.The trials themselves are conducted by CRO's that you will need to manage in terms of results and logistics.
Some travel will be involved up to once a month for a couple of days.
Responsibilities
You will be responsible for the operational management and oversight of the trial at the new study site. You are responsible for managing the project, the external partners and logistics involved. You establish milestones, track and report study progress. You are responsible for good, clear and positive communications with external parties and study staff.Requirements
- MSc in biomedical sciences or similar- 5+ years of trial management experience with CRO management knowledge
- Hands-on mentality in study progress, troubleshooting and generally open to go the extra mile when called upon
- Fluent in English
- Strong personality with emphatic management style
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Naut van Osnabrugge.
Dodatkowe informacje
- Ostatnia aktualizacja
- Wymiar etatu
- Pełny etat
- Rodzaj umowy
- Własna działalność
- Liczba wakatów
- 1
- Min. doświadczenie
- 2 lata
- Min. wykształcenie
- Wyższe licencjackie
- Branża / kategoria
- Praca Medycyna / Służba zdrowia / HealthTech