At Cure Science™ Institute, we work toward a future that is patient and data-centric to improve care delivery and develop cutting edge solutions. Our goal is to understand the disruption of the immune system by diseases and leverage omics technologies to develop personalized therapeutics. Please check out below open positions.
To Apply: Email your resume and cover letter to info@curescience.org
At this time, CureScience™ will not sponsor applicants for work visas or relocation. In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification document form upon hire.
Open Positions:
Job Descriptions:
Biomedical Engineer - Consultant
We are actively seeking an Engineer to join our growing team. This is an opportunity to work in an exciting and creative environment with an interdisciplinary team of individuals who are passionate about what they do. The Engineer will be responsible for developing and executing scientific research in the laboratory specifically related to the development of innovative devices and other technical opportunities.
Responsibilities
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Lead engineering aspects of clinical sciences primarily in the diagnostics and adjuvant technologies: exploration of new concepts, designing research strategy, design of circuits and devices etc. using Ultrasound, RF, Optics, Microfluidics etc.
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Hands-on approach exploring leading diagnostics strategies, developing interdisciplinary solutions.
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Lead IP strategy, write provisional patents, patents and other IP related activities, funding activities including monitoring agencies and opportunities, writing grants and developing strategy.
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Contribute to the strategic planning, design, development, implementation, and financial management of program objectives, procedures, processes and standards.
Qualifications
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MS or PhD in Bioengineering or other related fields with 3+ years of experience in research environment.
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Background and working knowledge RF, Ultrasound, Optics and Microfluidics etc.
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History of productivity as evidenced by publication peer-reviewed articles.
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Excellent problem-solving skills including critical and analytical thinking.
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Ability to independently design and execute experiments, interpret data, and identify appropriate follow-up strategies.
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Ability to multitask and work within timelines.
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Must be authorized to work in the United States.
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Provide three letters of recommendation.
Postdoctoral Research Scholar
The Postdoctoral Scholar will be responsible for carrying out investigational and experimental neuroscience research, with the goal of delivering cutting-edge advancements in discovery and development. This opportunity will offer a balance between learning and work experience that will allow individual development in translational research.
In this role, you will be conducting laboratory research applying cellular and molecular techniques to diagnostics and drug development, particularly for neurodegenerative diseases and neuro-oncology.
Responsibilities
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Working closely with scientists and research associates to design and independently execute in vitro experiments to support neurodiagnostics efforts, including biomarker identification and characterization, optimization, and validation.
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Responsible for implementation of in vitro studies and data collection and presentation of results as needed.
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Interpret internal and external data sets to assist in assay design.
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Present data results to leadership and to partners, collaborators, and donors to inform future decisions on potential research direction.
Qualifications
Basic Qualifications:
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PhD in Neuroscience, Cell biology or related field.
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Strong background in neurodegeneration and/or neuroscience.
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Proficiency in various cell culture systems required.
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Knowledge of molecular biology and/or biochemical techniques.
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History of productivity as evidenced by publication of scientific findings in peer-reviewed journals.
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Excellent problem-solving skills including critical and analytical thinking.
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Ability to independently design and execute experiments, interpret data, and identify appropriate follow-up strategies.
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Ability to multitask and work within timelines.
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Must be authorized to work in the United States.
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Provide three letters of recommendation.
Preferred Qualifications:
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Strong background knowledge in neurodegenerative disease and/or neuro-oncology.
Key Leadership Competencies:
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Builds strong relationships with peers.
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Learns fast, grasps the essence and can change course quickly where indicated.
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Raises the bar and is never satisfied with the status quo.
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Creates a learning environment, open to suggestions and experiments to drive the science in the field of interest.
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Embraces the ideas of others, nurtures innovation and manages innovation to reality to multitask and work within timelines.
Content Developer - Consultant
The marketing consultant will be responsible for digital engagement of stakeholders. This opportunity will offer a balance between learning and work experience that will allow individual development in translational research.
In this role, you will be responsible to develop engaging content that is broadly relevant to life sciences and healthcare. Specifically, the content needs to address disease centricity and patient centricity.
Responsibilities
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Working closely with scientists and research associates to design and independently develop relevant content.
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Develop and streamline all digital channels with a focus on seamless and frictionless engagement.
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Run platform specific marketing activities with data and metrics as guiding principle.
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Build analytics and insights for individual platforms with a goal of increasing engagement.
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Segment audience as appropriate and generate content to address the needs of segmented audience.
Qualifications
Basic Qualifications:
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BS degree in communication or sciences or related fields.
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Strong background in content generation.
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Strong proficiency in graphics, video and audio and other technologies.
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Basic knowledge of science or diseases or understanding of healthcare.
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History of productivity as evidenced by previous engagements.
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Excellent problem-solving skills including critical and analytical thinking.
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Ability to independently design and execute content deployment, interpret data, and identify appropriate follow-up strategies.
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Ability to multitask and work within timelines.
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Must be authorized to work in the United States.
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Provide three letters of recommendation.
Key Leadership Competencies:
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Builds strong relationships with peers.
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Learns quickly, grasps the essence and can change course efficiently when indicated.
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Raises the bar and is never satisfied with the status quo.
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Creates a learning environment, open to suggestions and experiments to drive the message.
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Embraces the ideas of others, nurtures innovation and manages innovation to reality to multitask and work within timelines.
Data Engineer – Healthcare (India)
CureScience™ is a US based research organization and actively seeking a Data Engineer to add to our growing team. This is an opportunity to work in an exciting and creative environment with an interdisciplinary team of individuals who are passionate about what they do. The Engineer will be responsible for developing and executing data related scientific research specifically related to the development of innovative devices and other tech opportunities. The Engineer will be working remotely.
Responsibilities
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Lead informatics related activities within life sciences, healthcare, and clinical sciences.
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Develop a data platform to showcase actionable insights from time series-based data sets. The data sets can be from wearables or other devices or publicly available.
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Develop computational pipelines, mathematical modeling, statistical analysis methods, and machine learning approaches as applied to clinical sciences.
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Serve as the primary collaborator for data visualization and analysis, and algorithms for data intensive problems.
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Summarizes and visualizes data analyses results in the form suitable for written reports, and makes preliminary interpretations of the data.
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Participates in scientific discussions and bridges research, collaborators and other internal/external research and clinical teams.
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Develop, test, and maintain modular software pipelines for genome sequencing, assembly, annotation, metagenomic analysis, and genotyping using high-throughput sequencing platforms.
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Manages data including loading and querying data from database systems, downloading omic data from public repositories, and transforming data to the necessary formats.
Qualifications
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BS in Engineering or bioinformatics with 3+ years of experience in data sciences related to healthcare or life sciences or clinical sciences (MS or PhD can be considered with less experience).
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Background and working knowledge of genomics or other omics.
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History of productivity as evidenced by publication peer-reviewed articles will be preferred.
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Excellent problem-solving skills including critical and analytical thinking.
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Ability to independently design and execute experiments, interpret data, and identify appropriate follow-up strategies.
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Ability to multitask and work within timelines.
Clinical Research Associate
We are currently recruiting a clinical research associate (CRA) for CureScience™. CureScience™ is a non-profit organization whose purpose is facilitate the advancement in personalized health care treatments focusing on cancer, immune, and neurological disorders. Working under direct supervision the CRA will help with coordinating and effectively maintaining diverse activities related to managing projects. Responsibilities include, but are not limited to patient screening, eligibility, registration, quality control of data compilation and submission, study evaluation, and managing cross-functional projects.
The CRA is responsible for coordinating and leading key projects simultaneously. The unique duties of this position will allow you to interact in a collaborative team environment where your main focus will be to support various research projects, implement process improvements, and manage technology transfer. In this role, you will be responsible for collecting and analyzing data, maintaining accurate source documentation, and prioritizing organizing, planning, tracking and coordinating the implementation of approved projects.
Responsibilities
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Work collaboratively with others in reviewing and managing protocols.
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Coordinates or performs project/activities as delegated.
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Support & assist in all aspects of clinical data management, including creation, and collection of source documentations, completion of case report forms, and tracking/reporting of serious adverse events.
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Captures/enters data into clinical trial database as necessary.
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Collects and maintains complete records and statistics on each research study patient.
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Knowledge of clinical trial components including screening, eligibility review, consenting, and ensuring completion of all protocol-required assessments.
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Serve as a resource liaison for investigators and other researchers involved in the day-to-day management of patients on clinical trials.
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Liaise with sponsors and other collaborators when applicable and coordinate study assessments and projects.
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Assist with the establishment and maintenance of procedures and systems (i.e. computerized database) for research coordination and data management.
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Assist to improve research information systems.
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Assures ongoing compliance with all system, regulatory, and federal regulations and department policies.
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Maintain research practices using Good Clinical Practice (GCP) guidelines.
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Participate in required training and education programs.
Qualifications
Basic Qualifications
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Bachelor’s Degree Required
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ACRP/SoCRA (or equivalent) certification preferred
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2-3-year project management experience
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Proficient in Microsoft Office Programs (i.e., Word, Excel, Outlook, and PowerPoint)
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Experience with Electronic Data Capture systems
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Research or clinical research data entry experience
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Must be authorized to work in the U.S.
Key Skills
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Thorough understanding of GCP and IHC regulations, clinical trial monitoring, and regulatory compliance required.
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Works well with others and possess excellent communication skills and problem-solving abilities.
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Highly organized and attentive to details.
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Ability to organize workflow and set priorities.
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Communicates well with patients, sponsors, collaborators, and staff on interpersonal and technical levels and demonstrates high integrity and confidentiality of all information.
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Experience in data collection, management and analysis, using web tools, regional databases, statistical software and spreadsheets.
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Able to manage multiple research projects within a fast-paced environment; able to collect and manage large amount of data and maintain databases; communicates progress, challenges, and results effectively.