• 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 plot maintenance and preparation- Preparing sites to include planting, maintaining, spraying and harvesting the research plots. • Prepare for training sessions or grower field days. • Grooming plots and planning protocol execution to coincide with these events is paramount. • Crop scouting/advising - Walk research plots to evaluate weed control, insect infestations and disease outbreaks, consulting with Agronomists or Technical Seed Managers on solutions, and planning operations to resolve issues with crop production. • Help train and guide summer interns to complete operational goals. • The Research Specialist develops workflows, task lists and trains summer interns on skills necessary to complete the work in a timely manner with exceptional quality. • Planning Activities – Assist research manager with planning and organizing the following: sourcing research sites, developing contracts, site layout, entry lists, database setup, equipment prep, fertilizer and crop protection planning, operational plans, and data flow planning. • Work with Land O’Lakes safety team to ensure DOT and Safety compliance. This includes tracking fuel receipts, RAIR compliance; ensuring proper logbook procedures are followed.

Role Description The Sr Clinical Research Associate (Sr CRA) ensures the effective management and monitoring of clinical studies in the site(s) assigned by the Clinical Operations Project Manager (COPM), while respecting the protocol and in accordance with the standards of local regulatory authorities, the rules of Good Clinical Practice (ICH / GCP) and Servier Standard Operating Procedures (SOPs). This position could act as the leading CRA for the CRA team, and will assist COPM in all projects set up and management aspects and require a proven record of hands-on experience in processes such as: - Study feasibility and site qualification - TMF and ISF set up - Creation of monitoring plans - Preparation of IRB submission packages Qualifications - Bachelor’s degree or equivalent education/experience preferred in Scientific/health care field - 5+ years of Clinical Operations experience (including Clinical Research Associate roles) within a pharmaceutical company or CRO - Knowledgeable of current FDA and IRBs regulatory requirements and guidelines governing clinical research - Ability to oversee, manage and communicate effectively with clinical sites - Strong attention to detail, establish priorities and meet deadlines - Ability to work independently and take initiative - Strong knowledge of applicable computer software applications - Strong interpersonal skill set necessary to create and maintain internal and external collaborator relationships Requirements - Implement and monitor site(s) in assigned study(ies) - Contribute to the site’s identification and selection process, conduct the site’s selection and qualification visits under the supervision of COPM - Take an active role in the creation of the study monitoring plan, reference documents for sites; review other study related manuals and supportive documents if needed - Ensure the preparation of the site before the initiation visit and carry out the initiation visit and related follow up actions including initiation visit report and follow-up letter - Participate in the development of the sites recruitment plan and closely monitor the progress of recruitment of site(s) - Assist in the creation of the Investigator Site File (ISF) - When applicable, lead the CRA team of a specific study to organize and carry out trainings to all site’s research teams on the study protocol and related tasks - Perform monitoring activities according to the study specific protocol and monitoring plan - At study level, monitor the progress of clinical trials and ensure the quality, reliability and authenticity of data collected according to protocol, Servier SOPs, regulatory requirements and GCPs of all sites with the supervision of COPM - Check the validity and consistency of the data collected in the e-CRF; manage correction requests if necessary and supervise corrections - Identify and manage deviations with the personnel concerned at the site(s) - Ensure the detection and careful monitoring of adverse events (AE) and serious adverse events (SAE) representing pharmacovigilance cases and ensure the transmission of information to the departments concerned - Manage the logistics of the investigative site(s) including investigational products, clinical materials and biological samples - Serve as technical support to the investigators and be the first point of contact with the site’s staff regarding the monitoring and resolution of problems encountered - Report all monitoring activities (update data in the various clinical data management systems), write visit reports and follow-up letters to investigators - Perform site(s) closure visit - Other duties as part of the Clinical Operations team and leading CRA for a team - Assist the COPM in organizing investigators meetings - Train newcomers in the team including CRA(s), VIE, CTA - Assist in the preparation of ISF binders - Actively involved with regulatory submission including the site’s ICF review and validation, under COPM’s supervision - Assist COPM for budget and contract negotiation - Participate to UAT for the systems used for assigned study(ies) - Participate in Data Review along with COPM for the assigned study(ies) - Collaborate actively with the other members of the project team (Medical Monitor, Clinical Medical Scientist, other CRAs, CTA, Data Management, PV, CLL, CSU and etc) when needed - Involve in the preparation of study(ies) audits / inspections, assist other CRA(s) in the preparation of site(s) audits/inspections - Respond to observations from audits/inspections and ensure the implementation of the corrective and preventive actions - At Hub level, actively involved in processes improvement and tools development - Function as SME for CRA or CRA referent for the Americas Hub Benefits - Salary range: $131,000-$150,000 - Short-Term and Long-Term incentive programs - Medical, dental, vision coverage - Flexible time off (unlimited sick time and flex time) - 401(k) plan - Life and disability insurance - Recognition programs

Role Description Dow Jones Energy provides price transparency across the global fuel supply chain, including the Spot, Wholesale Rack, and Retail markets. Dow Jones Energy enables customers to buy and sell energy commodities with confidence with multi-platform access to accurate data, real-time news, powerful software, and educational events. Our commitment to reliability is reinforced by personalized customer service and constant innovation. - Identify sales leads via direct and indirect client contact. - Cover chemical markets and provide market updates for weekly and monthly reports. - Supply/Demand - Maintain, update, and balance long forms up through entire product chains, short forms, and quarterlies as needed. - Perform presentations for clients both in our offices and onsite. - Maintain a detailed working knowledge of the basic databases and tools for responsible products (Supply/Demand, Global Pricing System, Capacity Data Base, and Trade Grids). - Econometrics - Maintenance and modifications for product-specific models. - Assets - Maintain product capacities based on market intelligence. - Actively pursue and develop unique analytical approaches that provide value to clients and/or potential clients. - Maintain and develop knowledge of state-of-the-art industry processes for specific product chain. - Involvement with long-term projects related to responsible products such as cost studies, etc. Qualifications - Bachelor's Degree or equivalent experience - Chemical Engineering, Chemistry, or Technical Preferred. - Minimum of 5 years of experience. - Previous work experience in a Petrochemicals company is a significant advantage. - Previous experience using analytical skills, ideally as a Business Analyst. - Experience in customer-facing roles is an advantage. - Chemical industry knowledge combined with a good level of product expertise. - Expertise with Microsoft Office products. - A conceptual understanding of how economics and politics influence regional and global markets. - Proficient public speaker. - Ability to think through questions and/or problems and independently provide solutions. - Proactive and self-motivated, focused on delivery of quality results. - Good team worker. Requirements - Write and proof text for weekly and monthly reports. - Ensure charts and price files are up to date for routine reports. - Update Price/Supply/Demand/Forecast sections for reports. - Update/create meaningful charts for reports. - Answer client questions about data and services. - Discover prices through industry contacts; maintain price forecasts both short and long term. - Update Supply Demand Quarterly balances and Trade reports. - Contribute to Long Forms, Supply Demand, Trade, and Quarterly balances to ensure they are completed, accurate, and up to date. - Keep consultants informed of the latest news or press releases related to their products. - Help with client requests as needed. - Assist in enabling accurate and timely publishing of all reports by maintaining accuracy of price and chart files and troubleshooting any publishing issues. Benefits - Comprehensive Healthcare Plans. - Paid Time Off. - Retirement Plans. - Comprehensive Insurance Plans. - Lifestyle programs & Wellness Resources. - Education Benefits. - Family Care Benefits & Caregiving Support. - Commuter Transit Program. - Subscription Discounts. - Employee Referral Program.