bhi logoCurrently reporting to the Vice President of Economic Development, the Senior Life Sciences BusinessStrategist evaluates the commercial potential of emerging technologies and provides recommendations ongo-to-market strategies.

This is a customer facing role with a focus on supporting clients in the development of commercial analysesand federal grant proposals.

The Senior Life Sciences Business Strategist also supervises junior Life Sciences Business Strategists andmanages consultants, as needed.

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NIH BHI LogoBioHealth Innovation, Inc. (BHI), is a Montgomery County innovation intermediary which translates market-relevant research into commercial success by bringing together management, funding, and markets.  BHI is seeking a life science business analyst to support the NIH SEED Office (https://seed.nih.gov/). The analyst will provide business landscape analysis and other project support on product development, corporate strategy, and private investment for NIH-funded companies. This will entail market landscape, technology, and other business intelligence research to support Entrepreneur-in-Residence and other SEED life science commercialization activities.

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DCM Logo

The Service Coordinator is the initial and primary point-of-contact for all DCM BioServices clients. They are responsible for interfacing with our clients and the DCM team to coordinate the delivery and reporting of all repairs and services. They also have a desire to provide the highest levels of client service, be an advocate for DCM BioServices, and be eager to drive growth.

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Nobile Life Sciences LogoIn this role you will: 

  1. Overall responsibility for the conduct of the assigned study as well as the interpretation, analysis, documentation, and reporting of results.
  2. Conducting the study in accordance with GLP regulations, the protocol, and Noble Life Sciences (NLS) SOPs.
  3. Defining: staffing, supplies, equipment, and space requirements for the study and assuring those test systems are as specified in the protocol.
  4. Notifying testing facility management which animal rooms and personnel will be required for the study.
  5. Preparing the study protocol and getting signed approval from the sponsor, testing facility manager, and pertinent subcontractors.
  6. Defining and coordinating subcontractor support requirements.
  7. Preparing IACUC documentation and submitting it to the IACUC committee for approval.

And Much More.... 

Nobile Life Sciences LogoIn this role you will: 

  • Serve as a Study Director for non-GLP and GLP-compliant Medical Device efficacy and toxicology studies.
  • Be responsible for study design and execution.
  • Supervise of technical staff.
  • Conduct data analysis and interpretation
  • Prepare study reports in compliance with regulatory requirements.
  • Study design, proposal preparation, and extensive interactions with sponsor representatives are essential functions.
  • Other related duties as assigned.

Nobile Life Sciences LogoIn this role you will: 

  • Serve as a Study Director for non-GLP and GLP-compliant non-clinical toxicology studies.
  • Be responsible for study design and execution.
  • Supervise of technical staff.
  • Conduct data analysis and interpretation
  • Prepare study reports in compliance with regulatory requirements.
  • Study design, proposal preparation, and extensive interactions with sponsor representatives are essential functions.
  • Other related duties as assigned.