Research Associate I - 4DBio³

The Geneva Foundation; Rockville (MD); On-site; USD 50,000 - 60,000; Full time

Job summary

A leading organization in research and biotechnology is seeking a Research Associate I to manage and enter data for various studies. The role involves interaction with research participants, support for study management, and coordination of research activities within the Uniformed Services University lab. Candidates should possess a Bachelor’s degree and relevant experience in research, demonstrating strong communication and organizational skills.

Qualifications

• Bachelor’s degree or equivalent work experience required.
• 2-4 years’ experience in research preferred.
• Experience in non-profit, research, or healthcare desired.

Responsibilities

• Collect and enter study data under supervision.
• Manage study documentation and ensure compliance.
• Coordinate data collection schedules and assist with participant recruitment.

Skills

Oral communication

Written communication

Organization

Attention to detail

Flexibility

Microsoft Excel

Education

Bachelor’s degree

Advanced degree

Job description

About The Position

The Research Associate I collects and enters study data under the supervision of the Principal Investigator. The Research Associate I has primary responsibility under the direction of the Principal Investigator for data extraction and entry in preparation for analysis.

The Research Associate I will work full time on-site at the Uniformed Services University (USU) Center for Biotechnology (4DBio³) Lab in Rockville, MD. Must be within a commutable distance to the Rockville Metro area. A thorough government background check will be administered. Those with active Security Clearances are encouraged to apply.

About The Project

The mission of 4DBio³ is to promote the development and application of advanced biotechnologies within the Department of Defense to enhance the readiness, health, and well-being of America’s Warfighters, veterans, and families. Capabilities include additive manufacturing with an emphasis on bioprinting, tissue engineering, cell culture and characterization, and product development.

Salary Range

$50,000 - $60,000. Salaries and hourly pay rates are determined based on several factors including external market data, internal equity, and the candidate’s related knowledge, skills, and abilities for the position.

Responsibilities

• Promote safety and confidentiality of research participants at all times
• Adhere to Occupational Safety and Health Administration (OSHA), Good Clinical Practices (GCP), Good Laboratory Practices (GLP), and infection control procedures
• Prepare research subjects (animal or human) for research study
• Execute and maintain research study
• Manage study documentation to include accurate and timely filing
• Prepare progress reports
• Document all correspondence and communication pertinent to the research
• Interact and communicate effectively with Principal Investigator, other site personnel, research participants, The Geneva Foundation, and the funding organization
• Procure supplies and equipment as authorized per research budget guidelines
• Comply with all the rules and regulations as applicable to assigned duty station
• Assist in all phases of the research project to include: recruit research participants, consent volunteers, administer questionnaires, prepare animal research, sanitize animal research areas
• Coordinate data collection schedules of all research team members
• Monitor budgets
• Create and adhere to a data quality and quality assurance plan
• Assist with interim and annual reports. S/he will be the primary liaison at the data collection site and will be responsible for explaining the project to military personnel associated with the study
• Make travel arrangements for consultants, when needed
• Schedule and attend regular team meetings
• Assist with the initial coding and data entry of structured questionnaires and data collection tools, when applicable
• Demonstrate proficiency in performing basic study related procedures (i.e., Vital Signs, ECG, phlebotomy, animal surgery) as required
• Recruit research participants, assist in enrollment and protocol procedures, monitor follow-up visits, oversee regulatory and administrative details, and provide data management assistance and project close-out support as applicable
• Complete required and applicable research training needed to complete research
• Maintain and update files of all applicable regulatory documentation for IACUC or IRB (including protocols, approvals, amendments, modifications, etc.) as well as any communications with the sponsor or any other Federal or regulatory office (including prior approvals, change in scope, etc.)
  
  
  

Qualifications

• Bachelor’s degree (Advanced degree preferred) or equivalent work experience required
• 2-4 years’ experience in research preferred
• 2-4 years non-profit, research, or healthcare experience desired
• Demonstrate competence in oral and written communication
• Must be organized, attentive to detail, and possess a positive, friendly and professional demeanor
• Must be flexible with changing priorities and able to communicate in a diplomatic and professional manner
• Computer skills including at least intermediate level experience with Excel and other Microsoft Office Software