Clinical Research Specialist Albany, NY – FT Position Available In Albany, New York

Employment Type:

Full time

Shift:

Day Shift Description:

Clinical Research Specialist•Albany, NY•

FT Position Highlights:

Quality of Life:

Where career opportunities and quality of life converge

Advancement:

Strong orientation program, generous tuition allowance and career development

Work/Life:

Monday•Friday, Office Hours What you will do: Plans and conducts research studies independently or in conjunction with investigators and clinical researchers. Performs background research and literature reviews to identify gaps in scientific knowledge. Develops hypotheses and designs studies to effectively test hypotheses. Drafts IRB proposals and works with the IRB on study proposal submissions. Reports on status of projects and maintains project timelines and study documentation. Gathers data, performs statistical analyses, and interprets results. Summarizes and disseminates study results through manuscript preparation/publication. Engages with scientific community and presents research findings at conferences. Contributes to grant applications through background research and/or writing.

Research Preparation:

Proposes ideas for new research studies to advance field based on literature reviews and/or observed gaps in clinical/scientific knowledge Formulates hypotheses and designs research studies to test hypotheses Serves as subject matter expert for clinical staff on research study design and statistical analysis Determines study-specific documentation requirements and prepares Institutional Review Board (IRB) submissions, consulting with the IRB liaison as needed Performs background research for studies and grant proposals Drafts and reviews study protocols Ensures that qualifying studies are registered as clinical trials Assists clinical staff with study planning according to study design, availability of resources, anticipated patient enrollment, and number of personnel assigned to participate in project

Research Project Management:

Conducts research studies, utilizing medical records, databases, prospective data collection, and other sources of information to compile, analyze, and evaluate data Ensures completeness of assessments/data sets Performs, or assists with, patient screening for study eligibility Administers informed consent to eligible patients Performs statistical analyses and interprets results Discusses findings with other personnel to evaluate validity

Data Management:

Oversees data collection and ensures fidelity of datasets Reports data collection progress and performs interim statistical analyses for dataset reevaluation as needed Ensures that datasets containing protected health information are shared in a HIPAA-compliant manner Maintains data files in an organized, confidential manner for easy retrieval and review Summarizes data and analyses in tables and figures for anticipated publication/presentation

Documentation Management:

Maintains protocol regulatory documents for compliance with IRB, including renewals, changes to open protocols, and submission of new protocols Prepares study records for audits by regulatory, accrediting, and research organizations Organizes and maintains all study-related documents, including informed consents, paper-based assessments, IRB submissions, and research training records for clinical staff Reporting Prepares manuscripts of completed projects for publication or for use in further research activities Coordinates the submission of manuscripts for publication in peer-reviewed journals, ensuring that all materials are compiled, formatted, and submitted in accordance with requirements and deadlines Addresses manuscript reviewer and editor comments in a timely manner Presents research findings at national conferences through poster or oral presentations Reports outcomes and prepares other statistical reports as requested What you will need: Bachelor’s in biology, clinical or scientific field required. Master’s degree or Ph.D. in clinical or scientific field preferred. Minimum five (5) years post-graduate research experience with at least 3 years in a clinical research setting preferred. Experience with research study design, data collection and analysis, and statistical analysis software. Experience with manuscript preparation and grant writing preferred.

Pay Range:

$33.10-48.00 Pay is based on experience, skills, and education. Exempt positions under the Fair Labor Standards Act (FLSA) will be paid within the base salary equivalent of the stated hourly rates. The pay range may also vary within the stated range based on location. Our Commitment Rooted in our Mission and Core Values, we honor the dignity of every person and recognize the unique perspectives, experiences, and talents each colleague brings. By finding common ground and embracing our differences, we grow stronger together and deliver more compassionate, person-centered care. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other status protected by federal, state, or local law.