Qureos Mentor

The Geneva Foundation

<div>About the Position
 
 
The Senior Clinical Research Coordinator (CRC) oversees and administers clinical research studies and associated activities. This position will assist with the development and management of study budgets. The Senior CRC will assist with the review of protocol requirements and assist with the collection of impact statements needed to properly assign costs to each assessment/procedure. The Senior CRC will provide feedback on the amount of time necessary for conduct staff to administer assessments and procedures as assigned during the budgeting process. The Senior CRC shall cooperate as necessary with the Geneva Corporate Manager to ensure that studies remain financially healthy, including but not limited to, the review of monthly budget reports as well as budget forecasts. The Senior CRC assists in project planning, and ensures that pre- established work scope, study protocol and regulatory requirements are followed. This position may recruit and coordinate research subjects, as appropriate, and serves as principal administrative liaison for the project. This position oversees and coordinates the provision of administrative and staff services to investigators; develops and maintains record keeping systems and procedures. The Senior CRC may also assist with the preparation of presentations for required review and approval processes, to include public
 
affairs office review as applicable.
 
 
About the Project 
 
This position will support multiple research projects under the MIRROR program. Musculoskeletal Injury Rehabilitation Research for Operational Readiness (MIRROR) delivers high value research, education, training, and infrastructure for over 40 clinically relevant musculoskeletal injury (MSI) studies within the military health system (MHS). MIRROR supports a broad scope of projects, including epidemiological investigation, investigator initiated pilots, and prospective randomized multisite clinical trials. Areas of clinical evaluation comprise general MSI care process models and highly prevalent anatomically-specific (e.g. back, knee, shoulder pain, etc.) targeted interventions with protocols examining effective return-to-duty activities. These studies particularly focus on deployment-limiting MSIs, ensuring that research addresses the challenges faced by service members in maintaining operational readiness. Results of these studies generate evidence-based approaches for future clinical practice guidelines as well as educational opportunities for future military and civilian providers at WRNMMC and USU. 
 
Compensation: $85,000 - $110,000
Qualifications<ul><li>
Bachelors degree or equivalent work experience required; masters degree preferred</li><li>
8 years&rsquo; experience in clinical research preferred</li><li>
5+ years non-profit, research, or healthcare experience desired</li><li>
Certified Clinical Research Coordinator (CCRC) certification preferred</li><li>
US Citizenship required to work at this government site</li><li>
Demonstrated competence in oral and written communication</li><li>
Must be organized, attentive to detail, and possess a positive, friendly and professional demeanor</li><li>
Must be flexible with changing priorities and able to communicate in a diplomatic and professional manner</li><li>
Computer skills including at least intermediate level experience with Excel and other Microsoft Office Software</li><li>
Knowledge of CFR, GCP and ICH guidelines</li></ul>
Management Responsibilities<ul><li>
May manage CRCs in entry-level to mid-level roles, research assistants, and other entry level to mid-level members of the conduct team, as assigned</li><li>
The following management responsibilities are applicable to the Senior CRC in a supervisory role:<ul><li>
Assist with staffing, hiring, salary negotiations and performance review process for conduct staff</li><li>
Conduct counseling, corrective action, up to and including termination, with Human Resources and Director</li><li>
Oversee programmatic/study related conduct ensuring staff perform tasks within scope of project</li><li>
Manage conduct staff to ensure optimal performance on each study</li><li>
Ensure staff demonstrate basic understanding of their job description</li><li>
Plan and facilitate individual and team meetings</li><li>
Assure all staff comply with Foundation and site policies, procedures and SOPs</li><li>
Proactively prepare and conduct site evaluation and study initiation visits</li><li>
Ensure sponsor and Geneva enrollment/milestones, study execution, and monitoring expectations are met on 100% of all studies</li><li>
Cognizant of and promotes networking opportunities with sponsors, subjects, and researchers</li></ul></li></ul>
Responsibilities<ul><li>
Promote safety and confidentiality of research participants at all times</li><li>
Adhere to Occupational Safety and Health Administration (OSHA), Good Clinical Practices (GCP), Good Laboratory Practices (GLP), and infection control procedures</li><li>
Plan and coordinate the initiation of research study protocol, and the implementation of operating policies and procedures</li><li>
Plan, implement and maintain data collection and analysis systems in support of research protocol; may coordinate the collection and analysis of research data</li><li>
Recruit, instruct and coordinate research subjects and/or volunteers, as appropriate to specific study objectives and work scope</li><li>
Coordinate the day-to-day activities of technical support staff specifically engaged in the carrying out of research/clinical protocol, as appropriate to the position; may perform aspects of research protocol, as required, in accordance with specified program objectives</li><li>
Organize and facilitate meetings, conferences, and other events associated with research activities; may perform and/or coordinate outreach activities, as appropriate to research objectives</li><li>
Document all correspondence and communication pertinent to the research</li><li>
Interact and communicate effectively with Principal Investigator, other site personnel, research participants, The Geneva Foundation, and the funding organization</li><li>
Comply with all the rules and regulations as applicable to assigned duty station</li><li>
Create and adhere to a data quality and quality assurance plan</li><li>
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</li><li>
Demonstrate proficiency in performing basic study related procedures</li><li>
Complete required and applicable research training needed to complete research</li><li>
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.</li><li>
Manage study budgets to ensure that projects remain financially healthy and viable</li><li>
Cooperative with institutional compliance and monitoring efforts related to the study(ies) and report instances of noncompliance to the PI and the institutional compliance office as appropriate. Coordinate and facilitate monitoring and auditing visits. Notify PI and appropriate institutional officials of external audits and inspections by FDA and sponsors.</li></ul></div>

Senior Clinical Research Coordinator

<div>At Geneva, we are always on the search for top talent. While this role is not associated with a current opening, one may become available in the near future. Resumes are reviewed on an ongoing basis, and you could be contacted for this role or similar, at anytime. 
 
About the Position 
 
The Bioinformatics Analyst will use computational and statistical tools to interpret vast biological datasets to support scientific research and discoveries. Duties will include designing algorithms, databases, collaborating with researchers, and analyze and communicate complex findings through visualizations and reports.
QUALIFICATIONS<ul><li>
Masters Degree in Bioinformatics, Computational Biology, Genetics, Pre-Med/Nursing, or a related scientific field preferred</li><li>
AHIC (Health Informatics Certification) is a plus</li><li>
1 year medical paraprofessional experience</li><li>
1 year working in clinical informationcs department at an accredited university</li><li>
Minimum 2-3 years of combined experience next generation sequencing (NGS) data analysis, adept in the development of Next-Generation Sequencing (NGS) analysis pipelines and large-scale data management and processing</li><li>
Minimum 3 years of experience in full software development life cycle with strong skills in software analysis, database design, data modeling, different data types architecture development and data management</li><li>
Experience working with internal and/or external stakeholders on solution design and implementation</li><li>
Programming languages: R, PHP, JavaScript, Perl, Python, SQL, Shell Scripting and Java. Computing Environments: HPC clusters, SLURM, Linux, Mac OS X, Windows</li><li>
Working knowledge of biomedical ontologies (i.e. UMLS, RxNorm, SNOMED CT)</li><li>
Working knowledge and understanding of unstructured, semi-structured, and structured healthcare data</li><li>
Strong familiarity with surgical and molecular pathology repotts, next-generation sequencing report, or clinician notes</li><li>
Demonstrated competency in oral and written communication</li><li>
Must be organized, attentive to detail and reliable, possess good judgment and a positive, friendly &amp; professional demeanor</li><li>
Must be flexible with changing priorities and able to communicate in a diplomatic and professional manner</li></ul>
RESPONSIBILITIES<ul><li>
Translate PI/study needs through design and configuration of software capabailities to deliver desired outcomes and customization of use</li><li>
Modify software application design as needed to meet PI/study needs</li><li>
Design &amp; implement algorithms fpr data processing, and develop &amp; maintain bioinformatics databases</li><li>
Work closely and collaborate with researchers, computer scientists, and others involved to design experiments and interpret results</li><li>
Utilizes high performance computing assets and large data bases (big data)</li><li>
Analyses of problems to develop integrated solutions involving computer hardware and software</li><li>
Applies theoretical expertise and innovation to create or apply new technology, such as adapting principles for applying computers to new uses</li><li>
Incorporate problem solving techniques to develop integrated solutions involving computer hardware and software</li><li>
Identify complex problems and review related information to develop and evaluate options and implement solutions</li><li>
Use logic and reasoning to identify the strengths and weaknesses of alternative solutions, conclusions or approaches to problems</li><li>
Perform highly complex network tasks and systems studies</li><li>
Analyze and compare existing systems and subsystems, and make recommendations to increase scope and performance</li><li>
Oversee laboratory information systems and develop new methods for analyzing large, complex data sets</li><li>
Maintain up-to-date knowledge of clinical informatics</li></ul></div>

BioInformatics Analyst

Join The Geneva Foundation and explore 2   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.

The Geneva Foundation

About Company

Senior Clinical Research Coordinator

BioInformatics Analyst