Career Opportunities: Research and Clinical

The following list shows current career opportunities at Boston Biomedical, including title, job description, qualifications, and information about how to apply for the position:

  • All
  • Clinical
  • CMC, Quality Assurance, and Regulatory
  • Preclinical
  • Research
Clinical

Biostatistician

The Biostatistician will provide statistical and analytical support for clinical trial activities and pre-clinical research. The position will involve communication and collaboration with Clinical and Preclinical project team members. Read More

Clinical

Clinical Medical Director MD/PhD

The Clinical Medical Director MD/PhD will be responsible for clinical strategy, and support for early and late stage clinical development programs. The successful applicant will participate in all aspects of ongoing clinical research programs. Read More

Clinical

Clinical Research Associate

The Clinical Research Associate (CRA) actively participates in a variety of activities to support and facilitate the efficient conduct of patient trials in our clinical research programs. Read More

Clinical

Clinical Safety Associate

We are looking for a detail-oriented clinical professional to join our growing Pharmacovigilance (PV) team as a Clinical Safety Associate (CSA). Read More

Clinical

Clinical Safety Project Manager

We are looking for a clinical research professional to join our growing Pharmacovigilance (PV) team as a Clinical Safety Project Manager (CSPM). Read More

Clinical

Head of Clinical Operations

An experienced clinical operations person who will prepare clinical trial budgets including resource projections along with operating procedures. Must be able to establish and implement the clinical strategy to meet business ventures. Read More

Clinical

Senior SAS Programmer

Programming includes edit checks, data mapping, and analysis. Minimum seven years experience including industry background. Read More

CMC, Quality Assurance, and Regulatory

Assistant Project Manager, CMC Management

Responsible for the coordination, implementation, execution, and completion of CMC aiRNA projects to ensure clinical supply and to deliver on CMC strategy and company goals. Read More

CMC, Quality Assurance, and Regulatory

Associate Director/ Director, Quality Assurance

Plans audit calendar, lead external and internal audits. Read More

CMC, Quality Assurance, and Regulatory

Associate Project Manager of Analytical Development, CMC Management

The Associate Project Manager of Analytical Development is responsible for the coordination, implementation, execution, and completion of CMC analytical projects to ensure clinical supply and to deliver on CMC strategy and company goals. Read More

CMC, Quality Assurance, and Regulatory

Associate Project Manager, CMC Management

Associate project manager is responsible for the coordination, implementation, execution, and completion of strategic projects and specific initiatives to ensure clinical supply and to deliver on CMC strategy and company goals. Read More

CMC, Quality Assurance, and Regulatory

Associate, Regulatory Affairs

Publishes regulatory submission documents such as INDs, NDAs and IMPDs Read More

CMC, Quality Assurance, and Regulatory

Laboratory Technician - CMC

Responsible to carry out laboratory experiments associated with CMC projects to deliver on CMC strategy and company goals. Read More

CMC, Quality Assurance, and Regulatory

Manager, Regulatory Affairs

Publishes and/or manages publishing regulatory submission documents such as INDs, NDAs and IMPDs Read More

CMC, Quality Assurance, and Regulatory

Project Manager, API Manufacturing

Primary duties will be hands-on in the laboratory and require extensive cross-functional collaboration within Pharmaceutical Sciences, as well as with Research, Manufacturing and contract manufacturing organizations (CMOs). Efforts will center on process chemistry, including process research and optimization, scale-up, process transfer, and process troubleshooting. Read More

CMC, Quality Assurance, and Regulatory

Regulatory Operations Assistant

Successful preparation and submission of IMPDs/CTAs/INDs, amendments/DSURs, and vigilance/safety reports. Read More

CMC, Quality Assurance, and Regulatory

Senior Manager of Analytical Development, CMC Management

Senior manager of analytical development is responsible for the coordination, implementation, execution, and completion of CMC analytical projects to ensure clinical supply and to deliver on CMC strategy and company goals. Read More

CMC, Quality Assurance, and Regulatory

Senior Manager, Manager – Quality Assurance

Plans and develops audit calendar/program, leads external and internal audits Read More

CMC, Quality Assurance, and Regulatory

Sr. CMC Scientist/Engineer, Clinical Drug Product Manufacturing

The Sr. CMC Scientist/Engineer will be responsible for global clinical drug product manufacturing projects from initial technology transfer through preparation for commercialization. He or she will collaborate with clinical supply planning, process development subject matter experts, and external partners to meet clinical supply needs, and facilitate drug product manufacture, packaging and labeling operations - including scheduling, finances, document review, and maintenance of relevant quality systems. Read More

Preclinical

Invivo Pharmacology Scientist

We are currently recruiting a Senior Scientist to join our growing Pharmacology / Preclinical Development group. Read More

Preclinical

Lab Coordinator

We are currently recruiting a Lab Coordinator to manage the daily operations of the Preclinical laboratory. Read More

Research

Associate Scientists, Protein Expression and Purification

We are currently seeking a highly motivated and enthusiastic protein expression and purification associate who will be part of an interdisciplinary team of scientists. Read More

Research

Bio-Programmer

The Bio-Programmer will be responsible for build and development of applications that will advance our core RNA silencing program. She or he will manage multiple assigned projects, collaborate with scientists, and communicate results in a timely fashion. Efforts will range from code optimization to big data challenges, as well as systems integration. Read More

Research

Bioinformatics Programmer

Develop, and implement using our proprietary state-of-the-art algorithm applications, and work-flows to grow our bioinformatics and RNA silencing capabilities and infrastructure. Read More

Research

Computational Biologist

The Computational Biologist position will assist in development of BBI’s RNA silencing program. This opportunity offers the chance to work on projects ranging from bioinformatics to structural biology, polymaths are highly sought. This individual will work collaboratively to further BBI’s pioneering research on our RNA silencing technology. Read More

Research

Formulation Scientist (PhD)

We are currently recruiting experienced Formulation Scientist(s) to join our growing Company. If you have experience in developing new proprietary formulations including small molecules and RNA based formulation development, skills in nanoparticles drug delivery including nanosuspension and nanoemulsions and have a track record of success in ability to work complex problems within formulation development and process tech transfers, you could qualify for this opportunity. Please include your publication/patent list on your CV when submitting. Read More

Research

Research / Postdoctoral Scientists (biomarker)

Research Scientists will join a face-paced and highly collaborative group working to bring first-in-class novel oncology drugs to market. Read More

Research

Research Scientists, Postdoctoral Scientists

Ph.D. or M.D. Expertise and experience on molecular biology, cell biology, microbiology, oncology, genomics, structure biology, chemical engineering, formulation, medicinal chemistry, pharmacology and bioinformatics are desirable. Read More

Current Clinical Trials

Our ongoing studies in advanced cancers emphasize inhibition of cancer stem cell pathways.Learn More