Clinical Trials Manager gene therapy
Location: NetherlandsSIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!Our client is a professional Clinical Research organisation, based in Utrecht Netherlands.
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.
- 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.
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.
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