Research Analyst

• Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance
• Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific actions; immediately communicates/escalates serious issues to the project team and develops action plans
• Maintains a working knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations, and company SOPs/processes
• Verifies the process of obtaining informed consent has been adequately performed and documented for each subject/patient, as required/appropriate
• Demonstrates diligence in protecting the confidentiality of each subject/patient
• 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
• Assesses site processes as per the Clinical Monitoring/Site Management Plan (CMP/SMP)
• Conducts Source Document Review of appropriate site source documents and medical records
• Verifies required clinical data entered in the case report form (CRF) is accurate and complete
• Applies query resolution techniques remotely and on site, and provides guidance to site staff as necessary, driving query resolution to closure within agreed timelines
• Utilizes available hardware and software to support the effective conduct of the clinical study data review and capture
• Verifies site compliance with electronic data capture requirements
• May perform 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
• Ensures the investigator/physician site is aware of the requirement of archiving essential documents in accordance with local guidelines and regulations
• Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs and Clinical Monitoring Plan/Site Management Plan
• Supports subject/patient recruitment, retention and awareness strategies
• For assigned activities, understands project scope, budgets, and timelines; manages site-level activities / communication to ensure project objectives, deliverables and timelines are met

Clinical Research Associate – Full-Service

• 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

• Provide support to the Head of Institutional Loans to build and manage a portfolio of institutional loans.
• Identify appropriate investment opportunities based on credit fundamentals of the issuer & sector and the bank’s credit risk appetite.
• Monitor the portfolio closely for financial & business updates and make timely buy, sell, hold recommendations.
• Work and present credits independently with minimal supervision and collaborate with the business, credit, internal audit and back office for credit approvals.
• Interact with senior management of portfolio companies & sponsors for investment diligence.
• Present new & existing credits at various credit committees at the bank.
• Provide on the job training in underwriting to junior members.
• Lead and/or participate in various technology & portfolio management projects.

Senior Research Analyst – Institutional Loans

• Ensure the capture of program data.
• Produce reports based on program data.
• Monitor the commitment and obligation of funds.
• Prepare reports on disbursement of funded research or demonstration projects.
• Help translate scientific evidence from the literature into practical information.
• Support ongoing coordination and management of program activity.

Research Analyst – Non-Data

• Develop SAS programs for validating surveillance, clinical, or research study data.
• Verify that all variables that should be included in the resulting dataset are present in the dataset and extraneous variables are excluded.
• Identify data discrepancies and other inconsistencies in the resulting dataset.
• Develop codebooks and data management plans.
• Run duplicate procedures and comparison of results to ensure validity with applicable standards of the resulting final data sets, indicators, questionnaire coding, metadata set, SAS programming, and output files.
• Conduct geospatial and molecular HIV analysis and interpret results using R.
• Work collaboratively with other analysts to develop novel code in support of analyses.
• Support dissemination and reporting of data to internal and external partners.
• Work alongside federal partners to support funded jurisdictions or funded CBOs.

Research Analyst, SAS, R

• function as an expert in the field of risk analysis
• perform security reviews and produce written and oral reports identifying risk
• support compilation and analysis of data
• conduct risk-based security reviews on non-U.S. Government personnel
• prepare and provide reports, analyses, and recommendations
• coordinate with stakeholders to schedule meetings and present findings.

Junior Operations Research Analyst

• Assist in the origination, underwriting, and monitoring of privately placed debt securities for institutional clients
• Perform in-depth due diligence including credit analysis, research, and financial modeling
• Prepare detailed investment memos and present recommendations for new investments
• Active management and surveillance of existing portfolio credits
• Engage with sell-side agents, sponsors and investment banks to build relationships
• Partner with various sales teams to drive broader business development

Senior Research Analyst

• Generate, analyze and adjust custom reports based on client needs.
• Produce proactive insights and game notes to support live broadcasts and pre/post game coverage.
• Utilize SQL code to generate charts and reports from robust data sets.
• Assist with QA and maintenance of the research tool and datasets.
• Utilize ticketing systems to communicate directly with clients as well as to internally track the progression of issues.
• Leverage sports knowledge to create data-driven insights for broadcasts.
• Meet time sensitive deadlines.
• Identify potential quality issues and escalate as needed.
• Perform other ad hoc duties as required.

Broadcast Research Analyst

• preparing images for evaluation
• classifying observed changes
• entering data into FDA compliant electronic case report forms
• participating in quality control exercises
• performing literature reviews and writing reports
• reviewing, analyzing, and interpreting data and/or documents results for presentations and/or reporting to internal and external audiences
• providing operational guidance on day-to-day activities of unit or program staff and/or student workers
• operating, cleaning, and maintaining organization of research equipment and research area
• tracking inventory levels and placing replenishment orders
• participating in the development, interpretation, and implementation of research methodology and materials
• conducting research experiments according to established research protocols

Research Specialist – Grader

• Provides market research support in compiling and publishing high quality, comprehensive analysis and research on individual corporations, industries, financial markets, and economic developments as assigned
• Compiles, analyzes, and evaluates data, conducting modeling on multiple data inputs related to assigned: companies/industries and/or financial markets and economic analysis research reports
• Assists in the development of valuation tools and provides advice to institutional clients
• Assists in the preparation of forecasting models
• Maintains and enhances financial models and databases
• Works closely with senior research leads on ongoing publication of research reports

Equity Research Associate – Clean Energy

• Serve as the primary point of contact between investigational sites and the sponsor
• Conduct all types of site visits, including selection, initiation, routine monitoring, and close-out
• Ensure site compliance with ICH-GCP, SOPs, and regulations
• Maintain up-to-date documentation in CTMS and eTMF systems
• Support and track site staff training and maintain compliance records
• Monitor patient safety, ensuring timely and accurate AE/SAE/PQC reporting
• Support subject recruitment and retention efforts at the site level
• Oversee drug accountability and ensure proper storage, return, or destruction
• Resolve data queries and drive timely, high-quality data entry
• Document site progress and escalate risks or issues to the clinical team
• Assist in tracking site budgets and ensuring timely site payments (as applicable)
• Collaborate with cross-functional partners including CTAs, LTMs, and CTMs

Senior Clinical Research Associate

• Coordinate and oversee clinical trial activities throughout the study lifecycle.
• Provide strategic guidance and oversight, mentoring junior staff and coordinating with management.
• Develop and maintain clinical trial documentation.
• Advanced clinical support, including document creation for product registration and statistical analysis of clinical trials.
• Create, implement and administer methods and procedures to enhance operations, as appropriate.
• Provide clinical feedback and knowledge to Regulatory Affairs in the creation of documents required for product registration and technical file (Clinical Evaluation Report).
• Oversee clinical trial operations and site performance.
• Clinical trials reports creation.
• Submission package readiness for Ethics Committees approval; including clinical protocols, design case report forms, patient and investigator brochure, informed consent form, among others.
• Verify that data entered on to the CRFs is consistent with patient clinical notes, known as source data/document verification, collecting completed CRF forms.
• Support and review of statistical plans for clinical trials
• Monitor any updates that may arise about ethical considerations, scientific principles, legislation and regulatory guidelines, and clinical evaluation process.
• Identify and communicate study-related risks and operational challenges
• Participate in continuous improvement initiatives related to clinical processes.

• 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

Senior Clinical Research Associate – CNS/Psychiatry

• 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 and reporting potential safety-related events
• Collaborate with top-tier colleagues from various backgrounds and specialties

Senior Clinical Research Associate – Oncology

• Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects
• Involved in all stages of the clinical study, including identifying potential sites, performing various study start-up activities, training sites, managing site activities, and closing down research activities
• Conduct study initiation visits (SIVs)
• Ensure compliance with obtaining informed consent and adhering to regulatory requirements

• 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

• Provide technical and research support to update UPENN ration balancing
• Expand and update a dairy decision tool suite incorporating on-farm production data
• Develop and launch a benchmarking tool for PA dairy farmers
• Investigate and apply new non-linear programming technique to existing tools
• Re-launch and modernize dairy decision dashboard program
• Development of crop optimization tool and economic opportunity program
• Develop robotic feeding optimizer program
• Perform additional duties as assigned

Research Specialist

• 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

• 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.

See all jobs on JobTailor

Clinical Research Associate – Full-Service

Senior Clinical Research Associate, Oncology

Clinical Research Associate

Senior Research Analyst – Institutional Loans

Research Analyst – Non-Data

Research Analyst, SAS, R

Junior Operations Research Analyst

Senior Research Analyst

Broadcast Research Analyst

Research Specialist – Grader

Equity Research Associate – Clean Energy

Senior Clinical Research Associate

Clinical Research Associate

Senior Clinical Research Associate – CNS/Psychiatry

Senior Clinical Research Associate – Oncology

Senior Clinical Research Associate – CNS/Psychiatry

Senior Clinical Research Associate – CNS/Rare Disease

Research Specialist

Investigative Research Analyst

Research Analyst Intern