Research Analyst

• 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.

Clinical Research Associate

• Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites
• Conduct pre-study and initiation visits
• Ensure informed consent procedures and protocol requirements are adhered to
• Monitor data for missing or implausible data
• Complete Serious Adverse Event (SAE) reporting
• Assist with training of new employees

Clinical Research Associate II, Phase I

• 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

• Function as an internal consultant and program manager in marketing, strategy, product development, customer loyalty, internal operations, and business development initiatives
• Work with leadership, project staff, and inter-departmental staff/management teams to define objectives and identify key issues for each assignment
• Oversee project work of other team members
• Synthesize results into actionable insights, implications, and management recommendations
• Involved in the implementation of new initiatives

Senior Market Research Consultant

• Provide context for clinical trials and connect stakeholders to investigative sites
• Train and motivate site staff and investigators
• Conduct site evaluations, training, and monitoring activities
• Customize site engagement strategies for assigned studies
• Gather local insights and utilize site engagement tools to measure impact
• Proactively assess risks and monitor activities for study performance
• Develop knowledge of therapeutic area and patient journey for recruitment
• Ensure quality of data and timely submission of safety events

Clinical Research Associate I

• Conduct all types of site visits—selection, initiation, monitoring, and close-out in alignment with contracted scope of work, GCP, and ICH guidelines
• Collaborate with site staff to implement and track subject recruitment strategies
• Deliver protocol and study-specific training to site personnel
• Assess site performance and adherence to the protocol
• Monitor study progress by tracking regulatory submissions and subject enrollment
• Ensure that essential documents are collected and maintained in accordance with regulatory standards
• Document site management activities, visit outcomes, and follow-up actions
• Work closely with cross-functional project teams to support study execution

• Assists in the preparation and submission of regulatory documents to the study sponsor and IRB, as required by the protocol and regulatory requirements.
• Assist in the conduct and documentation of study visits and protocol-specific testing/interviews according to the study protocol.
• Assists the research team in completing case report forms accurately and according to the protocol.

Cancer Clinical Research Specialist 1

• 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 maintain 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

• Lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.
• Monitor clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
• Conduct site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
• Collaborate with cross-functional teams to ensure timely and accurate data collection and reporting.
• Provide training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
• Build and maintain effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Senior Clinical Research Associate

• Acts as primary local company contact for assigned sites for specific trials.
• Develops meaningful site relationships through consistent collaborative communication and engagement.
• May participate in site feasibility and/or pre-trial site assessment visits
• Responsible for driving activities within site initiation and start-up, preparation and conduct of site monitoring (including remote monitoring), site management (by study specific systems and other reports/dashboards) and site/study close-out according to SOPs, Work Instructions (WIs) and policies.
• Responsible for the implementation of risk based monitoring approaches at the site level and to work with site to ensure timely resolution of issues found during monitoring visits.
• Ensures site staff are trained and the corresponding training records are complete and accurate at any time point during all trial phases.
• Responsible in close collaboration with study team for the activities during site activation phase to speed up the process and activate the site in the shortest possible timeframe.
• Ensure site compliance with study protocol, ICH-GCP, and local/country regulations
• Ensure ongoing adequacy of site (facilities, staff) for trial conduct
• Ensure source and other site documentation is adequate and in compliance with ALCOA-CCEA
• Involved with site level recruitment strategy and prioritization and implementation in partnership with other functional areas.
• Ensures site non-IMP study supplies are adequate for trial conduct.
• Ensures that clinical drug supplies are appropriately used, handled, and stored and returns are accurately inventoried and detailed.
• Oversees the appropriate destruction of clinical supplies.
• Ensures site staff complete data entry and resolve queries within expected timelines.
• Ensures validity and completeness of data collected at trial sites
• Ensures that all Adverse Events (AE) /Serious Adverse Events (SAEs) are reported within the required reporting timelines and documented as appropriate.
• Maintains complete, accurate and timely data and essential documents in relevant systems used for trial management.
• Fully documents trial related activities, in particular monitoring.
• Writes visit reports and follow-up letter in accordance with the SOPs.
• Promptly communicates relevant status information and issues to appropriate stakeholders.
• Reviews study files for completeness and ensures archiving retention requirements are met, including storage in a secure area at all times.
• Aligns with relevant training requirements.
• Act as local expert in assigned protocols.
• Develops therapeutic knowledge sufficient to support role and responsibilities.
• Works closely with CTL to ensure Corrective Action Preventative Action (CAPA) is completed for Quality Assurance (QA) site audits and for quality issues identified at the site during routine monitoring visits.
• Prepares trial sites for close out, conduct final close out visit.
• Establishes and maintains good working relationships with internal and external stakeholders in particular investigators, trial coordinators and other site staff.
• May participate in the Health Authority (HA) and IEC/IRB submission and notification processes as required/appropriate.

Clinical Research Associate II

• Conduct detailed research to identify and verify beneficiaries on deceased individuals' accounts
• Evaluate beneficiary eligibility including reviewing documents for compliance with legal standards such as ERISA where applicable
• Document research findings and maintain detailed records of all interactions and determinations in relevant systems
• Assist in the resolution of complex cases by working with legal and compliance teams as needed
• Process fund transfers from decedent accounts to beneficiary accounts in compliance with legal and regulatory requirements

🌐
Worldwide
❌ Jobs You've Hidden
⭐️ Saved Jobs
✅ Applied Jobs
✉️ Email Alerts
👤 Account
This job opening is no longer available.
Similar Jobs
Clinical Research Associate

🕒 March 16

ICON plc

10,000+ employees

💊 Pharmaceuticals

🧬 Biotechnology

⚕️ Healthcare Insurance

Website
LinkedIn
All Job Openings

Clinical Research Associate overseeing site compliance and monitoring oncology trials for a leading clinical research organization. Collaborating with teams and ensuring patient safety during clinical studies.

🇺🇸 United States – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🔬 Research Analyst

Clinical Research Associate

🕒 March 16

ICON plc

10,000+ employees

💊 Pharmaceuticals

🧬 Biotechnology

⚕️ Healthcare Insurance

Website
LinkedIn
All Job Openings

Clinical Research Associate monitoring Oncology studies at ICON. Serving as primary contact between investigational sites and sponsor, ensuring compliance and supporting subject recruitment.

🇺🇸 United States – Remote

💵 $91.3k - $114.2k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

🔬 Research Analyst

Clinical Research Associate

🕒 March 16

ICON plc

10,000+ employees

💊 Pharmaceuticals

🧬 Biotechnology

⚕️ Healthcare Insurance

Website
LinkedIn
All Job Openings

Clinical Research Associate managing investigational sites for a global clinical research organization. Ensuring compliance with protocols, regulations, and patient safety throughout study processes.

🇺🇸 United States – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🔬 Research Analyst

Clinical Research Associate

🕒 March 9

Vanguard Clinical, Inc.

51 - 200

🧬 Biotechnology

⚕️ Healthcare Insurance

💊 Pharmaceuticals

Website
LinkedIn
All Job Openings

Clinical Research Associate managing clinical sites and monitoring data for clinical trials at Vanguard Clinical. Reporting to the Director of Clinical Monitoring, focusing on data integrity and patient safety.

🇺🇸 United States – Remote

💵 $90k - $130k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

🔬 Research Analyst

Research Analyst

🕒 February 28

Omniscient Digital

11 - 50

🤝 B2B

🛍️ eCommerce

Website
LinkedIn
All Job Openings

Research Analyst transforming data into narratives for B2B SaaS companies at an organic growth agency. Collaborating with teams to deliver impactful research insights.

🇺🇸 United States – Remote

💵 $70k - $85k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

🔬 Research Analyst

Search More Research Analyst Jobs
🌐
Worldwide
Built by Lior Neu-ner. I'd love to hear your feedback — Get in touch via DM or support@remoterocketship.com
Search
Search Jobs by country
Search jobs by city
Search jobs by job title
Search entry-level jobs
Search junior-level jobs
Search senior-level jobs
Search jobs by tech stack
Search jobs by contract type
Search remote internships
Search remote part-time jobs
Remote jobs Anywhere in the World
Companies Hiring Anywhere in the World
Companies Hiring Sales People Anywhere in the World
Companies Hiring Software Engineers Anywhere in the World
Resources
Advice
Tips for finding remote jobs
Interview questions and answers
Resume examples
Cover letter examples
Post a job
Affiliates
Privacy policy
Terms of service
Job board SEO course
AI Apply Copilot
OpenClaw job finder
Jobs by Country
Remote jobs anywhere in the world (Worldwide remote jobs)
Remote jobs United States
Remote jobs Australia
Remote jobs Brazil
Remote jobs Canada
Remote jobs France
Remote jobs Ireland
Remote jobs Germany
Remote jobs Netherlands
Remote jobs Spain
Remote jobs UK
Popular Jobs
Remote data analyst jobs
Remote customer support jobs
Remote executive assistant jobs
Remote marketing jobs
Remote product designer jobs
Remote product manager jobs
Remote project manager jobs
Remote recruiter jobs
Remote sales jobs
Remote software engineer jobs
Jobs by Type
Remote full-time jobs
Remote part-time jobs
Remote contract jobs
Remote internship jobs
Remote entry-level jobs
Remote jobs with no experience required
Remote junior jobs (1-3 years of experience)
Digital nomad jobs
Remote jobs with no degree required
Freelance remote jobs
Temporary remote jobs
Remote jobs hiring now
Stay at home mom jobs

• 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

• Research criminal records in jurisdictions throughout the United States
• Report results according to Validity's formatting standards
• Ensure compliance with the Fair Credit Reporting Act
• Compile information from various research sources
• Follow local, state, and federal laws in reporting records
• Liaise with the Quality Assurance team

Research Specialist – Full-Time

• Oversee the management and tracking of clinical trial data to ensure accuracy, integrity, and completeness.
• Conduct site qualification visits, site monitoring visits, and study close-out visits. Provide support to site staff during audits or inspections.
• Ensure clinical trials are conducted in compliance with protocols, Good Clinical Practice (GCP), ICH guidelines, SOPs, and regulatory standards (FDA/DEA).
• Review and manage electronic Case Report Forms (eCRFs), ensuring data is accurate and aligned with study protocols.
• Assist in the development and maintenance of Case Report Forms (CRFs) and other study-related documents.
• Provide training to site personnel on study procedures, protocols, and regulatory requirements.
• Regularly review data entered into the Electronic Data Capture (EDC) system to ensure compliance with study protocols.
• Identify, address, and escalate any study-related risks, issues, or opportunities for improvements.
• Follow up with clinical sites to ensure that data collection is progressing as planned and all required documentation is completed.
• Ensure timely and accurate management of regulatory documents and maintain compliance with regulatory requirements.
• Engage with Key Opinion Leaders (KOLs) in the medical and research communities to stay informed on scientific research and clinical data.
• Stay up-to-date with the latest developments in scientific research and clinical data relevant to Kuros Biosciences.
• Review and track clinical trial-related invoices, ensuring accuracy and compliance.
• Contribute to the creation and maintenance of project plans for clinical trials, ensuring alignment with company policies and timelines.
• Work independently to complete tasks while ensuring alignment with team objectives, timelines, and expectations.
• Expected to travel 3-5 days per month for site visits and clinical trial support.

• Assist project teams in compiling and synthesizing information (e.g., conducting literature reviews and policy scans).
• Prepare and assist with primary source data collection through interviews, focus groups, and surveys; organize materials; and contribute to content development.
• Participate in the collection and review of research and evaluation data.
• Analyze quantitative and qualitative research data and contribute to the reporting and interpretation of findings.
• Prepare documents, portions of reports, briefs, charts, and graphs that describe and interpret findings of analyses.
• Support proposal writing and business development activities.
• Support project management tasks, including developing project timelines, coordinating meetings, and tracking project progress.

Research Associate, Healthcare Innovations

• 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
• Develop and update documentation to support the tax return calculations and other collateral
• Eventually lead or assist other leaders on team projects, as needed
• Provide support for the products we create through both direct and indirect communication channels

Senior Tax Research Specialist

• Assist project teams in compiling and synthesizing information (e.g., conducting literature reviews and policy scans)
• Prepare and assist with primary source data collection through interviews, focus groups, and surveys; organize materials; and contribute to content development
• Participate in the collection and review of research and evaluation data
• Analyze quantitative and qualitative research data and contribute to the reporting and interpretation of findings
• Prepare documents, portions of reports, briefs, charts, and graphs that describe and interpret findings of analyses
• Support proposal writing and business development activities
• Support project management tasks, including developing project timelines, coordinating meetings, and tracking project progress

Research Associate, Employment & Economic Opportunity Program

• Conduct literature reviews and contribute to evidence syntheses.
• Conduct quantitative and/or qualitative data collection under the guidance of senior researchers.
• Clean, code, and analyze data from interviews, observations, surveys, and administrative data using appropriate research methods and software.
• Support psychometric coordination and field test planning.
• Create, maintain, and use tracking systems.
• Process and coordinate item development report feedback from the client.
• Conduct item-level and passage-level test development quality-control reviews.
• Organize recurring test development and technical meetings.
• Draft and contribute to technical reports, policy briefs, memos, and presentations.
• Support project management tasks.
• Contribute to business development activities.

Industrial and Organizational Research Associate

• 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.

See all jobs on JobTailor

Clinical Research Associate

Clinical Research Associate II, Phase I

Research Specialist

Senior Market Research Consultant

Clinical Research Associate I

Clinical Research Associate

Cancer Clinical Research Specialist 1

Senior Talent Intelligence, Market Research Specialist

Senior Clinical Research Associate

Clinical Research Associate II

Research Specialist

Clinical Research Associate II

Clinical Research Associate II – FSP

Research Specialist – Full-Time

Clinical Research Associate

Research Associate, Healthcare Innovations

Senior Tax Research Specialist

Research Associate, Employment & Economic Opportunity Program

Industrial and Organizational Research Associate

Lead Research Analyst, Executive Intelligence