Clinical Trial Scientist

Interested in being part of one of the most dynamic pharmas within the Swiss Life Sciences industry? If so, we have a great opportunity for you!

As a Clinical Trial Scientist, you will be planning, setting-up, conducting, closing, and reporting of phase II and III clinical studies from a scientific perspective. Experience in answering HA/EC questions on protocol and ICF is a must as well as exposure to Neuro/CNS studies.

The Clinical Trial Scientist is a core member of the Clinical Trial team which is located in Switzerland. Although the current situation allows the people to work from home, the long-term scenario is to work on-site. Initially, the role is a 6 months contract and the possibilities of extension depend on performance and team budget.

The main responsibilities are:

• Providing input into and reviews cross-functional trial documents such as the SAP, ESP requirements and specifications, monitoring guidelines, data review manual as well as scientific input into responses for IRBs/ECs and Has;
• Performing literature searches as needed to keep knowledge up to date;
• Collaborates closely with the Clinical Trial Physician (Medical Director) on relevant trial-related activities.

We are looking for someone meeting the next criteria:

• PhD, PharmD, MSc or equivalent degree in life sciences or healthcare;
• At least 2 years of experience in clinical development in similar position with a focus on Neurosciences trials;
• Hands-on experience writing the protocol and/or ICF amendments.

In case you could be interested in hearing more on the role, do not hesitate in applying or feel free to contact me on ecordovagarcia@aerotek.com.