Research Analyst

• Conduct selection, initiation, monitoring, and close-out visits in line with GCP and ICH guidelines.
• Collaborate with sites to develop and track recruitment plans, ensuring project needs are met.
• Provide protocol and study training to sites, maintaining regular communication to manage expectations and address issues.
• Assess site practices for protocol adherence and regulatory compliance, escalating quality issues as needed.
• Oversee regulatory submissions, recruitment, enrollment, CRF completion, and data query resolution.
• Ensure all site documents are filed in the Trial Master File (TMF) and Investigator’s Site File (ISF) per GCP/ICH and local regulations.
• Generate visit reports, follow-up letters, and other necessary documentation.
• Mentor clinical staff through co-monitoring and training visits.
• Work closely with study team members to support project execution.

Senior Clinical Research Associate, Oncology

• Conduct site monitoring visits (initiation, routine, and close-out) to ensure compliance with the clinical protocol, GCP, and regulatory requirements.
• Assist in the preparation and review of essential trial documents, such as informed consent forms, case report forms, and investigator brochures.
• Collaborate with site staff to ensure proper documentation, timely data entry, and resolution of data queries.
• Assist in the identification, selection, and training of investigative sites.
• Maintain accurate and complete study files and records in accordance with GCP and company SOPs.
• Monitor study progress to ensure timelines and quality standards are met.
• Report site activities and findings to the Clinical Study Manager and escalate issues as necessary.
• Support regulatory submissions by preparing clinical trial applications and maintaining relevant documentation.
• Work collaboratively with cross-functional teams, including Regulatory Affairs, Quality Assurance, and Project Management, to achieve study objectives.

Clinical Research Associate

• The Research Analyst will report to the Manager of Global Evidence Management team and will play a key role in executing scientific research projects focused on evidence synthesis, meta-analysis, and real-world evidence.
• Conduct high-quality systematic literature reviews, meta-analyses, and outcomes research.
• Collaborate with broader Global Access, Value and Economics, Market Access and Customers Analytics, Clinical and Regulatory Affairs.
• Execute systematic literature reviews according to PRISMA methods and Cochrane guidelines.
• Perform meta-analyses using statistical analysis tools such as R software.
• Conduct real-world evidence studies and collaborate with cross-functional teams to translate research findings into actionable insights.
• Present data and findings clearly and effectively to internal and external stakeholders.
• Prepare scientific manuscripts, abstracts, posters, and presentations for peer-reviewed journals and conferences, ensuring compliance with relevant publication standards.

Research Analyst Intern

• Conduct and report all types of onsite monitoring visits
• Be involved in study startup (if applicable)
• Perform CRF review, source document verification and query resolution
• Be responsible for site communication and management
• Supervise study activities, timelines, and schedules on the country level
• Be a point of contact for in-house support services and vendors
• Be involved in quality control, such as compliance monitoring and reports review
• Participate in feasibility research
• Support regulatory team in preparing documents for study submissions

Senior Clinical Research Associate

• Act as the main line of communication between the project team, sponsor, and the site
• Build and maintain a good relationship with the site staff involved in the study conduct
• Prepare, conduct, and report site selection, initiation, routine monitoring and close-out visits
• Ensure that subject recruitment targets are timely defined, communicated, recorded and met, and project timelines are followed at site level
• Ensure accurate and timely information flow with trial sites on Adverse Events and protocol/process deviations
• Perform source data verification and follows up on data queries at site level; review and manage study risks on a site level
• Ensure proper handling, use, accountability, reconciliation, and return of all Investigational Product(s) and clinical study supplies on sites
• Review essential study documents and reconcile study Investigator Site File (ISF) / TMF at site level
• Ensures quality (data integrity and compliance) at site level
• Conduct site audit preparation visits and resolve site audit findings
• Participate in study site audits and client onsite visits, as required
• Ensure the flow of documents and study supplies between the project team, site and the Central/ Regional Laboratory/ Central Reviewer/ Warehouse
• Conduct project-specific training of site investigators
• Support preparation of Investigator newsletters
• Assist Site Management Associates in maintaining study-specific and corporate tracking systems at site level
• Support preparation of draft regulatory and ethics committee submission packages
• Support collection of IP-RED packages at site/country level
• Facilitate review and reconciliation of the study TMF on country and site levels

Clinical Research Associate II

• Lead Research and Evaluation Projects
• Manage multiple research and evaluation projects from planning through final deliverables
• Serve as a primary point of contact for clients and project partners
• Coordinate project timelines, budgets, communications, and deliverables
• Ensure research activities meet quality standards and project objectives
• Support business development efforts, including proposal writing and client relationship management
• Conduct Mixed-Methods Research
• Design and implement surveys, interviews, focus groups, and other data collection activities
• Support participant recruitment and stakeholder engagement efforts, including outreach to diverse and hard-to-reach populations
• Manage, clean, and organize quantitative and qualitative datasets
• Maintain data integrity, confidentiality, and compliance with research protocols
• Analyze Data and Communicate Findings
• Conduct rigorous qualitative and quantitative analyses using appropriate methodologies
• Develop charts, dashboards, visualizations, and other tools to support data interpretations
• Prepare reports, presentations, literature reviews, and client-facing deliverables
• Translate complex findings into clear, actionable recommendations
• Contribute to Team Success
• Mentor junior staff and support team development
• Supervise field staff, consultants, and project team members as needed
• Contribute to proposal development, business development initiatives, and client relationship management
• Participate in professional development, conferences, publications, and knowledge-sharing activities

Research Associate II

• Assist with survey design, questionnaires, and sampling to meet client objectives
• Act as the day-to-day contact for clients and project collaborators
• Coordinate and manage multiple projects at once, ensuring on-time and accurate delivery
• Partner with suppliers when needed to ensure high-quality data collection at reasonable costs
• Analyze and interpret final datasets, creating clear, visually engaging reports (PowerPoint or similar)
• Guide clients through findings using YouGov’s analytics tools and software

Research Associate

• Designs and performs moderately complex experiments with minimal input from supervisor to support the project.
• Independently analyzes data and summarizes experiments supporting a portion of the project.
• Where necessary, provides clear feedback to groups such as Software and Engineering on the outcome of the experiment.
• Understands experimental goal within the context of the overall project.
• Contributes to one or more of the following: the design of oligo systems, sample processing or assay formulation experiments.
• Executes experiments in one or more of the following areas: Support of the ADM, sequence file results processing or other software modules required to run the assay on the instrument.
• Designs and executes studies to support the optimum assay performance based on formulation.
• Generates documentation from these experiments to support regulatory submissions and or Marketing and Sales documents Product Development.

Research Associate III, R&D Oligonucleotide Synthesis

• Collect, analyze, and interpret data to generate actionable insights that inform the Total Rewards COE strategies and initiatives.
• Develop measurement frameworks to assess the impact of learning programs, leadership development initiatives, talent acquisition, performance & succession management programs, and key talent interventions.
• Conduct ROI studies and effectiveness evaluations for Total Rewards COE initiatives.
• Conduct comprehensive pay equity analysis across different demographics, present findings and develop the strategy to address any identified disparities.
• Ensure accuracy and integrity of data by maintaining standards and governance practices.
• Assist in the design, implementation, and maintenance of COE tools, templates, and methodologies.
• Utilize total rewards data (ex. compensation, benefits usage, promotion cycles) in conjunction with other PP data (ex. tenure, performance reviews) to identify at-risk employee segments and propose targeted retention strategies.
• Drive innovation by moving from standard reporting to building predictive models that forecast compensation and benefits trends.
• Collaborate with PP Business Partners, functional leaders, and key stakeholders to understand needs and areas for innovation.
• Respond to inquiries and provide guidance on COE processes, tools, and systems.
• Support change management and communication efforts related to COE projects.
• Partner with the Health & Welfare Solution Specialist to evaluate the return on investment (ROI) of existing benefits programs by analyzing participation rates, cost per hire, and employee satisfaction data.
• Partner with the Compensation & Retirement Solution Specialist to improve salary and bonus modeling processes to increase efficiency and accuracy in advanced comp cycles.
• Recommend process improvements and innovative solutions to enhance efficiency, support a best-in-class employee experience and drive adoption.
• Contribute to knowledge management by documenting and sharing COE resources and learnings.

Total Rewards COE Research Analyst

• Conduct phone surveys/interviews during business hours to obtain housing data in a region to be determined
• Establish & maintain relationships with builders’ sales agents using various forms of communication
• Perform internet research to collect current data on new home communities, as needed
• Ensure timely and accurate updates of assigned community records
• Maintain a reliable schedule and proper communication with the research manager

Part Time Residential Research Analyst

• Develop, administer, and implement environmental programs in accordance with applicable federal, state, and local governmental requirements
• Monitor pollution prevention activities, environmental compliance programs, and auditing efforts to ensure adherence to environmental regulations and company policies
• Conduct environmental studies and prepare environmental impact reports associated with new construction projects, facility modifications, operational processes, and permit changes
• Review and analyze environmental documentation issued by regulatory agencies and determine impacts to organizational operations and mission execution
• Develop and publish compliance strategies, guidance, and implementation requirements to ensure organizational readiness and regulatory alignment
• Evaluate proposed environmental regulations and policies to assess financial, industrial, operational, public, and environmental impacts
• Coordinate and interact directly with regulatory agencies and stakeholders to resolve environmental compliance issues and support permitting activities
• Represent HII and supported organizations during government, industry, and regulatory rule-making activities, meetings, and working groups
• Support energy resilience, sustainability, infrastructure modernization, and environmental stewardship initiatives aligned with Department of Defense priorities
• Provide leadership, mentorship, and technical guidance to engineering and environmental support personnel as required
• Prepare technical reports, briefings, risk assessments, and executive-level presentations supporting program leadership and customer engagements

Environmental Research Analyst

• Track proposed legislation, regulations, and public policy developments relevant to the firm's practice areas and client base; synthesize findings into timely, actionable intelligence.
• Research, draft, and produce in-depth reports, issue summaries, comparative analyses, and timelines on proposed laws and regulatory actions — proactively delivering intelligence before it is requested where possible.
• Leverage AI platforms and research tools to design and build systems for legislative monitoring, alerting, and stakeholder reporting; identify opportunities to expand and improve these systems over time.
• Provide research support across all practice groups and business units, responding to incoming requests with accuracy, thoroughness, and clear communication.
• Participate in the assessment and trialing of new research platforms and AI solutions; contribute to resource evaluations and provide informed recommendations.
• Collaborate effectively with peers to manage research requests received from attorneys, consultants and firm staff, contribute to department projects, and support the team's broader strategic goals.
• Assist with other research tasks and projects as required.

Research Specialist – Legislation Specialty

• Conduct in-depth external research, including competitor organizational mapping, geographic talent availability, compensation benchmarking, and skill trend analysis across AEC and adjacent industries.
• Identify emerging talent and capability risks and opportunities tied to the enterprise growth plan; produce capability heatmaps and tiered target lists that translate ambiguous business questions into precise recommendations.
• Build and deliver executive-ready narratives that combine internal signal with external market intelligence to inform workforce planning and business decisions.
• Help to build bench strength for future leadership needs, identifying and nurturing high-potential external talent well ahead of open roles.
• Execute best-in-class talent mappings for niche, competitive roles spanning technical disciplines, project leadership, and corporate functions.
• Partner with sourcing teams, recruiters, TA leadership, and hiring leaders to translate business goals into targeted sourcing strategies and prospect management approaches that strengthen long-term pipelines.
• Assist and actively participate in developing and maintaining directional dashboards and talent visibility tools that surface trends, measure effectiveness, and guide strategic pivots.
• Leverage AI, LLMs, and automation to enhance research speed, personalization, and depth—evaluating new technologies, testing workflows, and scaling what works across the global TA function.

Senior Talent Intelligence, Market Research Specialist

• 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.

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• Oversees all aspects of study site management to ensure patient safety is protected, quality of data generated by managed sites resulting in consistently low query levels and in acceptable Quality Assurance reports.
• Provides guidance at the site and project level towards audit readiness standards and supports preparation for audit and required follow-up actions.
• Updates, tracks and maintains study specific trial management tools/systems, and status reports.
• If required, manages site start up procedures including the feasibility and recruitment of potential investigators, preparation of EC/IRB submissions, collection and review of regulatory documents, review and adaptation in Patient Informed Consents, notifications to IRB, EC and regulatory authorities, as appropriate, translation of study related documentation, organization of meetings and other tasks as instructed by the Clinical Trial Manager/Project Manager.
• If required, assists the negotiation of study budgets and the execution of investigator contracts under directions of Site Contract Management department/designee.
• Verifies the process of obtaining informed consent has been adequately performed and documented for each subject/patient, as required/appropriate. Assesses factors that might affect subject/patient’s safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues.
• Independently conducts all forms of site visits, including pre-study/ qualification, initiation, routine monitoring, and close-out visits, in accordance with the protocol, local laws, ICH-GCP and Precision SOPs. Prepares and submits for review, accurate and timely monitoring reports from all site visits (on-site and remote).
• Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs, Clinical Monitoring Plan/Site Management Plan and client requirements. Supports subject/patient recruitment, retention and awareness strategies. Enters data into tracking systems as required to track all observations, ongoing status and assigned action items to resolution.
• Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness and completeness.
• Reconciles contents of the ISF with the Trial Master File (TMF). Ensures the investigator/physician site is aware of the requirement of archiving essential documents in accordance with local guidelines and regulations.
• Communicates effectively and proactively with both site personnel and Precision Project and Clinical Trial Management to relay protocol/study issues including any deviations and implements necessary actions in response to those issues.
• Develops and maintains good working relationship with investigators and study staff, serving as an ambassador to promote Precision high quality and professional image.
• Performs investigational product (IP) inventory, reconciliation and reviews storage and security.
• Verifies the IP has been dispensed and administered to subjects/patients according to the protocol.
• Verifies issues or risks associated with blinded or randomized information related to IP. Applies knowledge of GCP/local regulations and organizational procedures to ensure IP is appropriately (re)labelled, imported and released/returned.
• Performs data review activities, including remote EDC CRF and patient profiles review, query resolution, and assists data management and clinical data quality personnel to resolve data discrepancies.
• Identifies and processes Serious Adverse Events according to the procedures defined by the study team. Also demonstrates a full understanding of the SAE reporting process.
• Identifies site risks and escalates those to Clinical Trial Manager/Project Manager with suggested contingencies. Owns the timely and appropriate resolution of the risk with minimal support from project team.
• Prepares for and attends Investigator Meetings and/or sponsor face-to-face meetings. Participates in global clinical monitoring/project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according to the project specific requirements.
• Travels as necessary according to project needs.
• Performs other duties as assigned by management.

Clinical Research Associate II – FSP

• Works with a Clinical Research Coordinator, Research Program Administrator or Research Nurse to coordinate/implement study.
• Evaluates and abstracts clinical research data from source documents.
• Ensures compliance with protocol and overall clinical research objectives.
• Completes Case Report Forms (CRFs).
• Enters clinical research data into Electronic Data Systems (EDCs) that are provided by the sponsors.
• Provides supervised patient contact or patient contact for long term follow-up patients only.
• Assists with regulatory submissions to the Institutional Review Board (IRB) including submission of Adverse Events, Serious Adverse Events, and Safety Letters in accordance with local and federal guidelines.
• Assists with clinical trial budgets.
• Assists with patient research billing.
• Schedules patients for research visits and research procedures.
• Responsible for sample preparation and shipping and maintenance of study supplies and kits.
• Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board.
• Maintains research practices using Good Clinical Practice (GCP) guidelines.
• Maintains strict patient confidentiality according to HIPAA regulations and applicable law.
• Participates in required training and education programs.

Clinical Research Associate I – OBGYN

• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
• Collaborating with investigators and site staff to facilitate smooth study conduct.
• Performing data review and resolution of queries to maintain high-quality clinical data.
• Contributing to the preparation and review of study documentation, including protocols and clinical study reports.

• Conduct fundamental research on an assigned industry and 1 – 2 companies within the industry, supported by training and mentorship from our investment platform
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