AT THE FOREFRONT OF SCIENCE AND MEDICINE.

ContraFect Corporation is an equal opportunity employer. We recognize the power and importance of a diverse employee population and strongly encourage applicants with various experiences and backgrounds.

All qualified candidates are encouraged to apply.
  • All positions are full-time.
  • Salaries are commensurate with experience.
  • To Apply: Send cover letter describing your qualifications for the desired career opportunity (with #, please) and your resume/curriculum vitae to jobs@contrafect.com
  • No phone calls, please.
ContraFect Corporation, a vibrant and growing biotech company in Westchester County, NY, just outside of New York City, is building its scientific team to develop anti-infective therapies based on fully human monoclonal antibodies produced through phage display technology and anti-bacterial lysins.

ContraFect is seeking self-motivated, curious, collaborative individuals who want to grow with us in an environment that is both challenging and energetic. We are looking for individuals who want to contribute their talents, intellect, and personality to a team of committed and dedicated employees.


Career Opportunity #0027
Head of Preclinical Development and Toxicology
Position Summary: ContraFect Corporation is a seeking a Head of Preclinical Development and Toxicology with a strong toxicology and immunotoxicity background. Experience with pharmacokinetics also desired. Direct experience designing and managing animal toxicology studies and other safety studies, and managing external CROs, as well as other IND enabling activities, including generating reports for FDA submission.

Primary responsibilities include all aspects of Preclinical Development including the design, development and direction of toxicology, immunological, pharmacology and pharmacokinetics studies. The successful candidate will be an accomplished preclinical development scientist with biologics experience. Excellent planning, budgeting and project management skills are also needed.

Primary Responsibilities:

  • Provides strategic and hands-on management ensuring that toxicology studies are conducted in line with the appropriate regulatory guidelines and standards (FDA, WHO, GLP, and ISO).
  • Oversees and manages protocol preparation for toxicology studies.
  • Ensures that all safety testing plans, registration activities, government submissions, and design control activities are addressed in accordance with Research and Development requirements.
  • Design and management of nonclinical studies.
  • Initiates and manages contracts in conjunction with finance group, coordinates activities with select Contract Research Organizations (CROs) and academic collaborators for preclinical development in the areas of toxicology, pharmacology, pharmacokinetics.
  • Prepare reports, regulatory documents and INDs.
  • Works closely with other functional areas and colleagues to insure that all studies are performed in a quality, timely and scientific manner.
  • Provides preclinical expertise, and strategy, to multi-functional project teams as the preclinical representative.
* Ensures compliance with GCP, GMP, and regulatory guidelines.

Requirements and Job Qualifications:

  • Ph.D. in pharmacology, physiology or related discipline. DABT preferred.
  • Minimum of 10 years of pharmaceutical/biotechnology industry experience.
  • Minimum of 7 years hands-on expertise developing and managing preclinical studies including those performed at external CROs.
  • Mastery of preclinical drug development, strategies, practices and FDA regulations.
  • Experience with biologics and related immunological studies required.
  • Demonstrated proficiency in nonclinical study design and management.
  • Demonstrated results in preclinical development and a track record of successful IND, NDA and BLA filings.
  • Previous experience and success with choosing and managing relations with external contractors, including CROs.
  • Experience interacting with U.S. and European regulatory authorities required.
  • Experience with all phases of clinical development, including pre-IND through Phase IV programs and associated regulatory filings.
  • Excellent writing and language skills along with strong communication and team management skills.

To Apply: Send cover letter and resume or curriculum vitae to jobs@contrafect.com

No phone calls, please.

ContraFect Corporation is an equal opportunity employer. We recognize the power and importance of a diverse employee population and strongly encourage applicants with various experiences and backgrounds.


Career Opportunity #0028
Senior Associate Scientist in Virology
Employment Status: Full-Time

Join a dynamic, growing biotechnology company in Westchester County, NY, just outside of Manhattan. We are dedicated to the development of biological drugs for the prevention and treatment of infectious diseases.

We are seeking a motivated and productive Senior Associate Scientist to contribute to the Antibody Development Team that supports antibody discovery and characterization efforts. The qualified applicant is a conscientious and diligent scientist, who is flexible and able to work with day-to-day autonomy but as an integral team member. The Senior Research Associate will play a key role in development, optimization, execution and analysis of in vitro functional assays. This individual will be involved with assays designed to support a wide variety of antibody characterization experiments.

Work Description:
The successful candidate must possess a demonstrated experience in virology techniques, mammalian cell culture, virus neutralization, and ELISAs.

Experience with a broad array of experimental techniques encompassing protein characterization, in vitro functional assays, animal model of virus infection, antibody expression/purification, and molecular biology techniques would be highly preferred. The qualified candidate will be responsible for designing and implementing novel tools and assays as needed. A strong work ethic and organizational and communication skills, together with an ability to work well in a dynamic team environment are required. Excellent problem-solving skills and experience in experimental design is highly preferred. Experience with data analysis software including GraphPad Prism and Excel is preferred. The candidate will be responsible for maintaining a detailed and well-organized notebook, and will work close with other members of the group to attain project goals. The successful candidate will need to be self-motivated, possess excellent interpersonal and written communication skills and the ability to work effectively in a fast-paced environment. The qualified candidate will also be responsible for analyzing data, creating timelines, generating detailed reports, and preparing and presenting project results to diverse teams and management. Management/supervisory experience is ideal, but not required. Excellent oral and written communication skills are required. Able to effectively present scientific data and concepts to international standards is required.

A minimum of a B.S. in Immunology, Biochemistry, Virology, or a related field is required. A minimum of 5 years of laboratory experience, preferably in a pharmaceutical or industry setting is preferred.More experienced applicants with Master's or Ph.D. degrees are also encouraged to apply.

Salary and Title: Commensurate with experience.

To Apply: Send letter, resume or curriculum vitae to jobs@contrafect.com

No phone calls, please.

ContraFect Corporation is an equal opportunity employer. We recognize the power and importance of a diverse employee population and strongly encourage applicants with various experiences and backgrounds.


Career Opportunity #0029
Senior Research Associatein Microbiology/Immunology
Employment Status: Full-Time

Join a dynamic, growing biotechnology company in Westchester County, NY, just outside of Manhattan. We are dedicated to the development of biological drugs for the prevention and treatment of infectious diseases.

We are seeking a motivated and productive Senior Research Associate to contribute to the Microbiology Team that supports drug development and new drug discovery efforts. The qualified applicant is a conscientious and diligent scientist, who is flexible and able to work with day-to-day autonomy but as an integral team member. The Senior Research Associate will play a key role in development, optimization, execution and analysis of in vivomodels of infectious disease. This individual will also be involved with assays designed to support a wide variety of drug development experiments.

Work Description:
The successful candidate must possess a demonstrated experience in microbiology techniques and small rodentprocedures.

Experience with a broad array of experimental techniques encompassing protein characterization (ELISA, flow cytometry) and assay developmentwould be highly preferred. The qualified candidate will be responsible for designing and implementing novel tools and assays as needed.

A strong work ethic and organizational and communication skills, together with an ability to work well in a dynamic team environment are required. Excellent problem-solving skills and experience in experimental design is highly preferred. Experience with data analysis software including GraphPad Prism and Excel is preferred. The candidate will be responsible for maintaining a detailed and well-organized notebook, and will work close with other members of the group to attain project goals. The successful candidate will need to be self-motivated, possess excellent interpersonal and written communication skills and the ability to work effectively in a fast-paced environment. The qualified candidate will also be responsible for analyzing data, creating timelines, generating detailed reports, and preparing and presenting project results to diverse teams and management. Excellent oral and written communication skills are required. Able to effectively present scientific data and concepts to international standards is required.

A minimum of a B.S. in Immunology, Biochemistry, Microbiology, or a related field is required. A minimum of 2 years of laboratory experience, preferably in a pharmaceutical or industry setting, is required. More experienced applicants with Master's degrees are also encouraged to apply.

Salary and Title: Commensurate with experience.

To Apply: Send letter, resume or curriculum vitae to jobs@contrafect.com

No phone calls, please.

ContraFect Corporation is an equal opportunity employer. We recognize the power and importance of a diverse employee population and strongly encourage applicants with various experiences and backgrounds.