• Conducts legal, business, and other research and reference work, including sophisticated, in-depth research and analysis utilizing legal and non-legal information resources • Conducts effective reference interviews and distills research results into clear and concise reports of findings • Evaluates diverse information sources for currency, reliability, relevance, and cost-effectiveness and selects the optimal resources for research requests • Assists in the instruction of attorneys, legal assistants, and others in the use of legal research tools and services • Maintains research proficiency across a wide spectrum of business, legal, legislative, analytics and docket resources including Lexis, Westlaw, Bloomberg Law, Pacer, WK VitalLaw, and Lex Machina among others • Effectively utilizes request tracking software to track and process research requests • Continues professional development through library association membership and activities

• Lead research strategy, including systematic market mapping and target company identification. • Build and maintain high-quality candidate pipelines. • Achieve 80%+ mapping accuracy through disciplined and creative sourcing methods. • Conduct first-round candidate interviews. • Contribute to structured candidate assessment and slate construction. • Produce client-ready candidate summaries and search materials. • Maintain disciplined search workflow and data integrity.

Role Description Brado’s Senior Qualitative Insight Specialist (IS) has already established a career in research and strategy, executing research to better understand consumers and customers. The Senior Qualitative IS is learning to translate research into strategy at all phases of the project. They execute research and develop and polish project deliverables under the leadership of a more senior strategist, learning to perfect their expertise in both research and strategy. Key Areas of Responsibility - Projects: - Accountable for ensuring all assigned aspects of the project are delivered on time and against client objectives. - Thinks proactively throughout the project to anticipate and quickly escalates and addresses changes to approach, design, objectives, etc. - Supports the design of studies and contributes to writing proposals. - Thoughtfully crafts questionnaires/discussion guides with appropriate techniques and activities, and structures of questions that better address objectives and fit with participant type. - Effectively moderates 1:1 and group interviews and online engagements (Communities, Remesh, etc.), spending typically 15% of their time doing live moderation. - Demonstrates an ability to connect the dots, identifying emerging themes and how they connect to the bigger story. - Incorporates and suggests strategic elements for the report including the story flow, emerging implications (so-what), and recommendations (now-what). - Begins to determine appropriate visual elements to communicate the story. - Demonstrates the ability to leverage client/industry knowledge and external frameworks (e.g., Michael Porter's Five Forces, The Habit Loop), anecdotes (i.e., metaphor and story), constructs, macro and micro-trends, psychological understanding, etc., to elevate the strategy. - Writes succinctly, to the audience, with clarity, conviction, and tension as well as polish and professionalism. - Client Relationships: - Demonstrates a confident, professional, respectful, agile presence when engaging with the client. - Develops rapport and builds empathy for and with the client, leading to long-term relationships. - Develops and continually seeks to deepen understanding of the client's business and the individual client to ask the right questions, anticipate needs. - Stays calm and collected even with difficult clients, and escalates challenges as needed. - Insight Department Activities: - Supports department specific initiatives. - Develops positive relationships with clients and other Brado teams. - Successfully represents Brado in external facing settings (e.g., conferences, new business presentations or networking events). Qualifications - 3+ years experience moderating and delivering excellent client deliverables in a market research or agency setting. - Bachelor’s Degree ideally in business, journalism, marketing, economics, social sciences (psychology, anthropology, sociology). - Pharmaceutical, med tech/med device, and consumer health market research experience with patients and healthcare professionals is a strong plus. - Willingness to travel (up to 25% of your time) and be flexible in scheduling to accommodate project needs. - Aligns with and Models our values: People, Commitment, Aspiration, Trustworthiness & Impact. Benefits - Health Care Plan (Medical, Dental & Vision). - Retirement Plan (401k, IRA). - Life Insurance (Basic, Voluntary & AD&D). - Paid Time Off (Vacation, Sick & Public Holidays). - Family Leave (Maternity, Paternity). - Short Term & Long Term Disability. - Training & Development. - Work From Home.

Role Description Ensure clinical trials are conducted and reported in accordance with all applicable regulatory requirements. - Provide cross functional operational support throughout the study lifecycle, investigating data or documentation discrepancies and contributing to process improvements that reduce recurrence during study conduct and closeout. - Support and coordinate study start up activities, including tracking site readiness, managing essential document collection, and communicating with sites regarding planning and logistics for Site Qualification Visits (SQVs) and Site Initiation Visits (SIVs). - Perform remote monitoring visits (qualification, initiation, interim monitoring, close-out) and complete reports as per study monitoring plan. - Support, interface, and collaborate with site personnel, IRBs/ECs, contractors/vendors, and cross-function company personnel. - Build and maintain strong working relationships with internal partners (Clinical Operations, Regulatory Affairs, Quality, R&D) and site personnel (Investigators, CRCs, research nurses) to support enrollment, data quality, and site performance. - Assist with any site remediation activities, as applicable. - Complete and maintain relevant global Medical and Clinical Affairs, BU-specific, and study-specific training. - Assist in identifying opportunities and proposing solutions to improve process efficiency within and across related functional areas. Qualifications - Bachelor's Degree or Equivalent Life Sciences or Nursing. - 3-4 years in clinical research (as a CRC or CRA) including quality assurance/control and regulatory compliance with experience in the healthcare industry. - Experience with electronic data capture. Requirements - Veeva experience or like platform. - Clinical research experience. - Data collections. - Domestic travel - 3 sites per year. Benefits - Contract on W2 (Need US Citizens or GC Holders or GC EAD or OPT or EAD or CPT). - First 6 months 30 hours per week then after this 25 hours per week. - Working hours are flexible (EST/PST, etc.). - REMOTE position.