Research Analyst

• Support a team of Investigators by conducting extensive research across multiple sources and tools.
• Research companies and individuals for case development using various investigative mediums.
• Conduct confidential background and due diligence investigations.
• Manage a large caseload and attorney requests in a dynamic and fast-paced environment.
• Collaborate with team members to support high-priority requests and cases.
• Assist with special projects as needed as an integral member of the Investigative Services Team.

Investigative Research Analyst

• Develop and maintain control structures to ensure data accuracy and quality across upstream and downstream systems
• Conduct data integrity gap analyses and partner with business and IT teams to resolve discrepancies
• Prepare monthly and quarterly claims analytics reports for leadership
• Analyze key performance indicators and support data‑driven decision‑making across the Claims organization
• Support fraud detection, subrogation analysis, medical management reviews, and legal analytics
• Collaborate with business stakeholders to understand requirements and develop tailored data solutions
• Present findings in a clear, concise, and visually compelling format

Insurance Claims Data Analyst

• 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

• Drives understanding and delivery of quality clinical research for all monitoring and site management activities
• Takes ownership to deliver upon near-term USO Clinical Development (CDO) goals, including successful delivery of studies within the clinical trial portfolio
• Delivers all relevant services/tasks in support of the planning and implementation of quality-driven clinical trials, in line with established targets and strategies
• Implements proactive risk identification and mitigation planning for assigned clinical trial sites
• Verifies safety reporting and the proper handling, monitoring and storage of trial products
• Ensures accuracy, validity and completeness of data collected at clinical trial sites
• Develops therapeutic area knowledge sufficient to support role and responsibilities
• Drives recruitment and retention strategies to support clinical trial sites to meet country enrollment and retention targets
• Participates in the preparation, conduct and follow-up of audit and inspection activities

Clinical Research Associate

• Support the day-to-day management of a media measurement panel, including executing regular operational processes
• Analyse data trends to identify issues and opportunities for improvement
• Investigate client queries and provide clear, timely responses
• Collaborate with internal teams to develop and improve workflows
• Support ongoing innovation by testing new panel features and processes

Research Analyst, Behavioral Panels

• Oversee all aspects of clinical monitoring and site management in compliance with GCP, global regulatory requirements, and WEP Clinical SOPs.
• Conduct on-site and remote monitoring to ensure protocol adherence, maintain essential documentation, and keep site and patient data inspection-ready.
• Build strong relationships with sponsors and sites, serving as a key point of contact throughout the study.
• Support development of study-specific procedures (e.g., Monitoring Plans) and assist in training or coordinating other CRAs.

Senior Clinical Research Associate

• Performing selection, initiation, interim monitoring and closeout visits (remote and onsite)
• Driving performance at the sites
• Proactively identifying and ensuring timely resolution to study-related issues
• Training, supporting and advising Investigators and site staff
• Development of recruitment plans with each site
• Ensuring timely collection/uploading of essential documents into the eTMF

Senior Clinical Research Associate – East Coast, NY/NJ

• Lead design and execution of equity‑centered RWD/RWE projects by therapeutic area that quantify disease burden, access, testing, treatment patterns, and outcomes across under‑represented populations.
• Develop mixed‑methods studies (EHR/claims analyses, registry data, SDoH integration, patient surveys, and qualitative interviews) and ensure outputs are timed to inform clinical programs, as well as relevant policy and commercial colleagues.
• Work cross-functionally to develop study protocols, statistical analysis plans, and methodological approaches that address selection bias, missingness in race/ethnicity/SDOH variables, causal inference, and subgroup inference.
• Integrate policy analysis into evidence generation: identify policy levers (e.g., Medicaid policy, payer coverage, reimbursement pathways) and translate study findings into policy recommendations.
• Manage strategic external collaborations and vendor relationships: identify and evaluate data partners, MSIs, FQHCs, safety‑net hospitals, community‑based organizations.
• Co‑lead co‑development of primary research with external partners (MSIs, FQHCs, community organizations) to ensure non‑extractive, trust‑based engagement and sustainable relationships that support recruitment and retention and post‑study continuity of care.
• Work closely with embedded/internal cross-functional partners to translate evidence into protocol design recommendations, site selection guidance, eligibility optimization, and outreach strategies.
• Produce actionable deliverables: TA‑specific, equity-centric RWD/RWE publications and plain language summaries and dissemination materials for both scientific and non‑technical audiences.
• Present findings to internal forums and to external stakeholders; publish in peer‑reviewed journals and present at scientific conferences.
• Mentor and build capacity across the HER Champion community; contribute to HER learning materials, SharePoint resources, and training modules.
• Ensure research adheres to ethical standards, privacy/regulatory requirements (HIPAA/GDPR where applicable), and community engagement best practices.

Health Equity Research Associate Director

• Research changes to tax forms
• Interpret the tax code and regulation updates that drove those changes
• Provide guidance to programmers on updates needed to calculations based on research findings
• Test tax return calculations for accuracy, consistency, and usability
• Design and execute test cases to confirm correct implementation of tax law changes
• Contribute to release notes, technical explanations, and customer-facing guidance as needed
• Develop working knowledge of assigned jurisdictions or tax topics and assist the team by applying that knowledge
• Develop and update documentation to support the tax return calculations and other collateral
• Provide support for the products created through both direct and indirect communication channels

Associate Tax Research Specialist

• Covering the NJ/PA Area
• Advance AbbVie's pipeline by striving for excellence in clinical research, turning science into medicine for our patients and leveraging new advanced capabilities to drive industry leading performance.
• Partners with the investigator and site staff for meaningful and effective engagements positioning AbbVie as the choice in clinical trials.
• Focus on site clinical research that ensures appropriate conduct of the trial while driving improvement in data integrity, compliance, overall study performance and customer experience.
• Considered as the primary point of contact for the investigative site.
• High level of competency or experience in providing contextual information on the clinical trials, connects stakeholder to the investigative sites and strengthens AbbVie’s positioning.
• Aligns, trains and motivates the site staff and principal investigator on the goals of the clinical trial program, protocol and patient treatment principles for the trial ensuring a trusted partnership.
• Conducts site evaluation, site training, routine, and site closure monitoring activities with compliance to the protocol and monitoring plans, in accordance with applicable regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), and quality standards, ensuring safety and protection of study subjects.
• Advanced understanding of site engagement and ability to customize site engagement strategy for assigned study (ies).
• Gather local/site insights and utilize site engagement tools such as the Customer Relationship Management (CRM) tool, to report/track progress and measure impact of that strategy.
• Advanced level of competency connecting the study protocol, scientific principles and clinical trial requirements to the day-to-day clinical trial execution activities.
• Evaluate and ensure effective recruitment and retention techniques/plans based on the patient disease journey.
• Develop solid knowledge of therapeutic area, asset and clinical landscape / patient journey to enable successful patient recruitment and overall protocol compliance.
• Possesses experienced level of competency to mentor and train less experienced CRAs on various aspects of work and provides input into their development.
• May participate in global/local task forces and initiatives.
• Responsible for activities as assigned by manager.
• Responsible for continuous risk-assessment proactively, and in collaboration with Central Monitoring team, monitor activities conducted by clinical sites to detect early overall study performance or patient safety issues.
• Advanced ability to think critically to resolve site risk signals while having robust understanding of site processes to drive study execution.
• Ensures preventative and corrective action plans are put into place, as needed, to mitigate risk and promote compliance using a customer centric approach.
• Identifies, evaluates and recommends new/potential investigators/sites on an ongoing basis.
• Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel.
• Ensures audit and regulatory inspection readiness at assigned clinical site at all times.
• Manages investigator payments as per executed contract obligations, as applicable.

Clinical Research Associate II

• Engage in extensive training with senior Clinical Research Associates and Managers
• Conduct clinical monitoring visits in accordance with study protocol and regulations
• Suggest ideas to improve site recruitment plans
• Create and maintain appropriate documentation regarding site management
• Manage the progress of assigned studies by tracking regulatory submissions and approvals

Clinical Research Associate I

• Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required
• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work
• Work with sites to adapt, drive, and track subject recruitment plans
• Administer protocol and related study training to assigned sites
• Evaluate the quality and integrity of study site practices
• Manage the progress of assigned studies by tracking regulatory submissions and approvals
• Ensure copies/originals (as required) site documents are available for filing
• Create and maintain appropriate documentation regarding site management
• Collaborate and liaise with study team members for project execution support

Clinical Research Associate – Sponsor Dedicated

• The Senior Clinical Research Associate (Sr. CRA) has local responsibility for the delivery of the studies at allocated sites.
• The Sr. CRA works in close collaboration with (Project Management Clinical Operations (PMCO), Study Start-Up (SSU) manager, Clinical Study Assistant (CSA) and other CRAs)
• The Sr. CRA acts as the main contact with the study site and is responsible for monitoring study conduct.
• Performing selection, initiation, interim monitoring and closeout visits (remote and onsite).
• Proactively identifying and ensuring timely resolution to study-related issues.
• Training, supporting and advising Investigators and site staff in study related matters.
• Development of recruitment plans with each site and managing enrollment to ensure sites meet enrollment milestones.
• Prepare and finalize monitoring visit reports in CTMS.

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Investigative Research Analyst

Insurance Claims Data Analyst

Research Specialist

Clinical Research Associate

Research Analyst, Behavioral Panels

Senior Clinical Research Associate

Senior Clinical Research Associate – East Coast, NY/NJ

Health Equity Research Associate Director

Associate Tax Research Specialist

Clinical Research Associate II

Clinical Research Associate I

Clinical Research Associate – Sponsor Dedicated

Senior Clinical Research Associate – East Coast, NY/NJ