Responsibilities and duties
- Contribute to scientific R&D and CMC projects through hands-on design, monitoring, and analysis of laboratory experiments.
- Contribute to approve Vendor, CRO and/or research universities initial and extension contract scoping. Check for milestones, deliverables and invoices.
- Conduct regular scientific updates to the Genflow Leadership Team
- Contribute to the execution of academic collaboration
- Accurately record and present scientific results through the completion of laboratory records, written reports, and presentations.
- Direct verbal and written communications with vendors and investigators, researchers and authors;
- Manage project deliverables within timelines and within the approved budget;
- Ensure of compliance with applicable regulations and guidelines throughout activities;
- Develop / improve of procedural documents and processes.
- Conduct logistical and administrative work (teams coordination, organize shipment, order material).
Qualifications
- Life science degree (e.g. Biology, Chemistry, Pharmacy, Bio-medical sciences), or equivalent experience
- Ph.D. or equivalent experience
Experience
- Thorough knowledge of the drug development process is essential
- Experience and deep expertise in molecular and cellular biology ideally in a drug discovery environment
- Experience in relevant laboratory techniques including: immunoassays (ELISA, Western Blot), qRT-PCR, flow cytometry
Required Skills
- Team player with the ability to work independently
- Strategic thinker and decision maker with open mindset
- Leadership, proven conflict management and negotiation skills
- Ability to interpret, analyze and translate interdisciplinary information
- Strong organizational, communication and motivational skill
- Analytical, pro-active, problem solving, and flexible
- Good time and project management
- Excellent communication skills and a personable nature to support relationship building within the team and with key stakeholders.
- Fluency in French and English is essential