Research Analyst

• Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects
• Conduct study initiation visits (SIVs)
• Ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements
• Perform various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets
• Train sites to collect data properly and report any potential safety-related events
• Manage the site's activities during study maintenance and closing down research activities at the sites once the study has concluded

Senior Clinical Research Associate – CNS/Rare Disease

• Contribute to construction and QC of longitudinal electronic health record (EHR) analytic files using structured data
• Conduct descriptive analyses of patient demographics, lab values, medication use, and clinical characteristics
• Summarize data availability, follow-up patterns, and measurement frequency across CKD subgroups
• Support feasibility assessments by generating counts, proportions, and distributional summaries
• Produce clean, well-documented analytic code and contribute to draft tables and figures
• Participate in biweekly internal team meetings and client meetings, and contribute to written deliverables

Contingent Summer Research Analyst Intern

• Conduct deep-dive investigative research into applicant information by cross-referencing multiple internal and external data sources to verify business legitimacy and financial health
• Analyze discrepancies in applicant documentation and independently resolve complex verification issues by applying sound critical thinking and judgment
• Maintain high standards of accuracy and thoroughness while meeting daily production benchmarks in a fast-paced fintech environment
• Partner with underwriting and partner relations teams to provide clear, actionable insights derived from your research, supporting Credibly’s goal of accelerated, right-sized capital solutions
• Identify and document patterns of risk or process inefficiencies to support platform enhancements and improve data quality

Risk Research Specialist I

• Considered as the primary point of contact for the investigative site
• Conducts site evaluation, site training, routine, and site closure monitoring activities
• Aligns, trains and motivates the site staff and principal investigator
• Develop solid knowledge of therapeutic area, asset and clinical landscape / patient journey
• Ensures quality of data submitted from study sites
• Protect study subjects' safety
• Manages investigator payments as per executed contract obligations

Clinical Research Associate II – Oncology

• Conducting thorough research into an individuals’ background using a variety of tools, such as databases and public records
• Gathering information, analyzing data, and compiling this information to be entered into a final report
• Processing searches related to background screening reports
• Ensuring all searches are processed and reported according to state and federal laws as outlined in AccuSourceHR’s reporting guidelines
• Ensuring all searches are processed according to client guidelines
• Retrieving public records information and entering said information into our platform
• Analyzing information and comparing data sets to confirm matching identifiers
• Performing other duties as assigned
• Meeting or exceeding minimum standard service requirements

Research Specialist

• Execute and maintain industry-specific talent mappings.
• Analyze the velocity of the technology market to identify emerging skill gaps.
• Author comprehensive intelligence reports for senior leadership.
• Act as a key consultant to HR and Business Unit leaders.
• Bridge the gap between internal talent pipelines and external market availability.
• Maintain a pulse on the 'Who’s Who' of the industry.

Lead Research Analyst, Executive Intelligence

• Use computers effectively to enter, access, and retrieve data
• Work in a fast-paced environment
• Be responsible for adhering to daily minimum production levels

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Senior Clinical Research Associate – CNS/Rare Disease

Contingent Summer Research Analyst Intern

Risk Research Specialist I

Clinical Research Associate II – Oncology

Research Specialist

Lead Research Analyst, Executive Intelligence

Risk Research Specialist I