Clinical trial manager (ONC) - permanent or freelance
Are you looking to work as a Clinical Trial Manager in an innovative biotech company developing products in the field of oncology? My client is a company using genetic engineering in the fight against cancer. They have a big pipeline of products that are in the early stages (preclinical and phase I) and you can be joining this company now to help manage these products throughout the whole clinical process. Working for my client means working in an exciting environment while you increase your value on the market as you will gain experience in innovative research in oncology.
As a clinical trial manager your responsibilities would be to; select and activate chosen study sites, establish and maintain an excellent relationship with site investigators and research teams; create and update activities in overall project plan on a regular basis to assure appropriate outcome of clinical trial projects in terms of scope, time lines and objectives; coordination of assigned CRA monitoring activities; ensure study quality/GCP compliance to deliver a rigorous patient data; partner with Clin Ops Director and provide oversight to all vendors or study delivery team, ensuring timely delivery of milestones and budget compliancy; propose and implement study process improvements; Participate in the preparation, updating and training of SOPs; liaise with manufacturing, central lab, and other study project stakeholders as needed; prepare all external and internal documentation for assigned trials ensuring it is completed in accordance with the study protocol, internal SOP's and GCP requirements (e.g., Patient Informed Consent Forms, Monitoring Plans, Project Plans); work with the Clin Ops Team to develop and maintain study time lines; be responsible for ensuring vendors deliver according to scope of work and review/approve vendor invoices
What we are looking for:
- Degree in Life Science, biological science, health (nursing, nutrition) or related area: or equivalent relevant experience acquired within life science industries
- At least 4 years' experience in clinical project management, including early phase
- Therapeutic area of expertise in oncology/haematology trials is a big plus
- Strong knowledge of ICH and GCP rules and of the complete clinical trials process
- Prior Biotech experience is a plus
If this job sounds interesting to you, please apply here or send your CV to me, Sofie Thijs, via the web page of NonStop consulting. You can find me on Linked In as well. If you are not available but you know someone that would be interested, please forward this to them and help out the people in your network!
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