Looking for various consulting/analysis/planning work done on a regulatory preclinical and Phase I chemotherapy I/O drug development (solid tumors - especially gastrointestinal and pulmonary).
Already working with big names such as Covance, but looking to add a more flexible individual to the core team for miscellaneous work related to above and/or for scientific writing (grants, pitches) related to above.
Please ping me with your brief profile (maybe LinkedIn or a local CV) and we can discuss more details.
As stated, the tasks are various and so we welcome interest from anyone who believes that he/she can help with at least some part of the above.
Potentially will go for FDA first.
Core team based in EU.
UPD: you must have a life science education and experience in basic or translational research or medicine/clinic.
26 freelancers are bidding on average €34/hour for this job
Hi, I am a medical writer with in depth knowledge in health and medicine having a medical background. I would be keen on joining your team and writing articles for you. With due consideration, we can discuss further.
PhD thesis in Life Science, MSc in Biomedicine, BSc in Molecular Biology and Physiology. University Teaching Assistant, vast experience in scientific research and writing.