The World Leader In Serving Science
Research Associate I - Patient-Centered Research
Location
Mexico
Posted
25 days ago
Salary
0
Seniority
Entry Level
Job Description
Research Associate I - Patient-Centered Research
Thermo Fisher Scientific
Title: Research Associate I - Patient-Centered Research Location: Remote Mexico Full time Join Us as a Research Associate I Evidera– Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. What You'll Do: • Assist with preparing proposals, protocols, and reports by conducting internet and literature searches. • Conduct literature reviews by abstracting data from scientific articles. • Participate in and oversee site recruitment, site contracting and IRB submissions, site management, and site training (including tracking enrollment and scheduling). • Manage data, including performing data entry and review. Assist with data analysis, including preparing qualitative code books, performing and overseeing coding, and reviewing quantitative data tables. Conduct one-on-one cognitive interviews and co-moderating focus groups; compile data collection tools. Handle data extraction (epidemiological and clinical data); model programming (larger parts of models). • Perform efficient delegation and communication within and outside of the project team. • Assist with financial management. • Provide scientific support in the implementation of simulation models (e.g., discrete event simulation) and other decision-analytic models (e.g., Markov, individual state-transition, survival partition) to assess the cost-effectiveness of healthcare interventions. • Assist project managers on multiple projects including drafting sections of project deliverables (reports, dossiers, protocols, spreadsheets, etc.) and participate in abstract, manuscript preparation, project proposals (e.g., gathering relevant material, drafting background sections, conducting scoping searches, and developing project budgets). • Participate in client meetings and prepare meeting minutes. Education and Experience Requirements: • Master’s Degree in scientific discipline and at least one year of experience in healthcare research; or Bachelor’s Degree in scientific discipline and at least two years of experience in healthcare research. • Coursework in implementation science and/or experience with implementation science studies In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. Knowledge, Skills, Abilities: • Good knowledge of Microsoft Office • Basic understanding of research methods • Basic knowledge of implementation science theories, models, and frameworks and/or behavioral theories, models and frameworks • Know how to multitask • Good communication skills • Problem-solving mindset • Attention to detail • Ability to work well within a team Working Environment: Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role: • Travel 10–30% of the time
Related Guides
Related Categories
Related Job Pages
More Research Analyst Jobs
Statistical & Psychology Research SME
Saratoga Medical CenterSaratoga Medical Center, based in New York City, New York, is a minority and women-owned professional services agency. Since 1985, Saratoga Medical Center has b
Role Description Saratoga Medical has an exciting opportunity for a Statistical & Psychology Research SME, Remote. This is a great full-time opportunity, 40 hours work week schedule, Monday to Friday, excluding Federal holidays. Qualifications - Master’s degree in Research Psychology, I/O Psychology, or related field (mandatory) - 5+ years of experience in: - Statistical analysis (JMP, SPSS, R) - Database development & data management - Research reporting (presentations, publications, technical reports) - Managing research design & methodology - Strong experience in human performance research - U.S. Citizenship required (no Green Card) Requirements - Must-Have Requirements: - Master’s degree in Research Psychology, I/O Psychology, or related field (mandatory) - 5+ years of experience in: - Statistical analysis (JMP, SPSS, R) - Database development & data management - Research reporting (presentations, publications, technical reports) - Managing research design & methodology - Strong experience in human performance research - U.S. Citizenship required (no Green Card) Benefits - Competitive rate - Paid time off - Benefit options Company Description Saratoga Medical Center, Inc. is an equal opportunity employer and will not discriminate in recruiting, hiring, training, promotion, transfer, discharge, compensation or any other term or condition of employment on the basis of race, religion, color, age (over age 39), sex, national origin, or on the basis of disability if the employee can perform the essential functions of the job, with a reasonable accommodation if necessary.
Role Description The Research Analyst will provide research and analytical support to the IT-Non-IT Workgroup (ITW) within the Veterans Health Administration (VHA). This role is critical in facilitating the IT and non-IT-related initiatives by offering comprehensive research, analysis, and report preparation for decision-making. The Research Analyst will work closely with various stakeholders to ensure the accurate delivery of project goals by supporting funded and unfunded IT/non-IT initiatives within VHA. This individual will engage in frequent interaction with VHA IT governance bodies and play a pivotal role in ensuring the success of key projects. - Data Collection and Analysis: Conduct in-depth research to gather data relevant to IT and non-IT projects. Analyze complex datasets to generate actionable insights and recommendations. - Reporting: Prepare and present detailed reports, briefing materials, and updates for ITW leads, stakeholders, and VHA executive leadership. Maintain precise documentation to support strategic decisions. - Project Support: Assist with the development of project plans, schedules, deliverables, and key performance indicators (KPIs) for various initiatives within ITW. - Meeting Coordination: Organize and provide logistical support for ITW meetings and briefings, ensuring proper communication with stakeholders. - Documentation Management: Maintain documentation of research findings, project updates, and meeting minutes, ensuring accessibility and traceability of project artifacts. - Support for IT/Non-IT Initiatives: Facilitate the progression of both IT and non-IT projects, ensuring alignment with VHA's strategic objectives and adherence to governance processes. Qualifications - Bachelor's degree in Research, Data Analytics, Information Technology, Healthcare Management, or a related field. - At least 3 years of experience in research and data analysis, preferably within the healthcare or government sector. - Must have prior acquisition and budget experience with a federal agency. - Must have VHA IT acquisition experience. - Strong analytical, problem-solving, and decision-making abilities. - Proven capability to translate data into insights that support strategic decisions. - Proficiency with Microsoft Office Suite, particularly Excel, PowerPoint, and data analysis tools. - Excellent written and verbal communication skills with experience presenting to leadership. - Familiarity with IT and non-IT project funding processes within the VHA or other federal institutions. - Knowledge of the New Service Request (NSR) and Multi-Year Programming (MYP) processes. Benefits - Health Care Plan (Medical, Dental & Vision) - Retirement Plan (401k, IRA) - Life Insurance (Basic, Voluntary & AD&D) - Paid Time Off (Vacation, Sick & Public Holidays) - Short Term & Long Term Disability - Training & Development
• Develop strong site relationships and ensures continuity of site relationships through all phases of the trial. • Performs, with oversight, clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documents. • Gain in-depth understanding of the study protocol and related procedures. • Coordinate & manage various tasks in collaboration with other internal roles to achieve Site Readiness. • Participate & provide input on site selection and validation activities. • Perform remote and on-site monitoring & oversight activities using various tools to ensure: • Data generated at site are complete, accurate and unbiased. • Subjects’ right, safety and well-being are protected. • Conducts site visits including but not limited to evaluation visits, initiation visits, monitoring visits, close-out visits and records clear, comprehensive and accurate visit & non-visit contact reports appropriately in a timely manner. • Collect, review, and monitor required regulatory documentation for study start-up, study maintenance and study close-out. • Communicate with Investigators and site staff on issues related to protocol conduct, recruitment, retention, protocol deviations, regulatory documentation, site audits/inspections and overall site performance. • Identify, assess and resolve site performance, quality or compliance problems and escalates as appropriate in collaboration with Clinical Research Lead and CRA line manager. • Manage and maintain information and documentation in CTMS, eTMF and various other systems as appropriate and per timelines. • Supports audit/inspection activities as needed. • Travel Requirements up to 75%.
• Develop strong site relationships and ensures continuity of site relationships through all phases of the trial. • Performs, with oversight, clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documents. • Gain in-depth understanding of the study protocol and related procedures. • Coordinate & manage various tasks in collaboration with other internal roles to achieve Site Readiness. • Participate & provide input on site selection and validation activities. • Perform remote and on-site monitoring & oversight activities using various tools to ensure: • Data generated at site are complete, accurate and unbiased • Subjects’ right, safety and well-being are protected • Conducts site visits including but not limited to evaluation visits, initiation visits, monitoring visits, close-out visits and records clear, comprehensive and accurate visit & non-visit contact reports appropriately in a timely manner. • Collect, review, and monitor required regulatory documentation for study start-up, study maintenance and study close-out. • Communicate with Investigators and site staff on issues related to protocol conduct, recruitment, retention, protocol deviations, regulatory documentation, site audits/inspections and overall site performance. • Identify, assess and resolve site performance, quality or compliance problems and escalates as appropriate in collaboration with Clinical Research Lead and CRA line manager. • Manage and maintain information and documentation in CTMS, eTMF and various other systems as appropriate and per timelines. • Supports audit/inspection activities as needed. • Travel Requirements up to 75%. • Adhere to all aspects of Ora’s quality system. • Adhere to all essential systems and processes that are required at Ora to maintain compliance to Ora’s data integrity & business ethics and regulatory requirements. • Clear and sustained demonstration of Ora’s values -- prioritizing kindness, operational excellence, cultivating joy and scientific rigor – as well as their linked behaviors.
