EPM Scientific is partnering up with fast growing global leader within the biotech industry.
A biotech company with several Phase 1 immune-oncology programmes is currently looking to expand their global research team. They need people to bring unique treatments into the clinics and design the trials with the pre-clinical team.
The company is an antibody discovery and development biotechnology company located in Geneva, Switzerland. Their focus is the development of therapeutic antibody-based approaches using a proprietary technology platform.
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Key Responsibilities:
โข Liaise with pharmacology research team to coordinate the preclinical dossier of bispecific antibody-based clinical lead therapeutic molecules targeting the tumor microenvironment in cancer
โข Lead efforts on preclinical data generation, interpretation, and communication
โข Contribute to the writing of non-clinical pharmacology study reports, investigator brochures, IND applications, regulatory annual reports, and other regulatory documents when appropriate
โข Work within the cross-functional clinical team to plan, execute and oversee early phase clinical trials in patients
โข Participate in Immuno-oncology team meetings to present data and provide analysis
โข Coordinate external collaborations and/or contract research laboratory services
โข Collaborate closely with the CMO in the execution of oncology clinical trials. Participate in drafting clinical protocol synopses, clinical protocols
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Skills and competencies:
โข An advanced degree such as M.D. or P.H.D. in cancer biology, immunooncology, or equivalent advanced biology degree
โข At least 3 years of industry experience in oncology drug development (small molecule and biologics), clinical research experience is required
โข Knowledge of translational research with an understanding of applications to cancer drug development is required
โข Experienced scientist with strong background in immunology and cancer immunotherapy, and knowledgeable in human and mouse tumor pharmacology
โข A good understanding of clinical pharmacology considerations in biologics development
โข The ability to work in a team environment and adhere to the highest personal and ethical standards with a commitment to GCP clinical research
You can apply here or by sending your application with a CV to Tihana.Sujica@phaidoninternational.com
