Manager, Research Services
$49.86 - $74.81 per hourGoodwin Procter
Join Goodwin’s Global Operations Team, and make a real impact on a global scale. At Goodwin, we work with some of the world’s most successful and innovative investors, entrepreneurs and disruptors in the life sciences, private equity, real estate, technology and financial industries, and where they converge. As part of the Global Operations Team – all business professionals at the firm – you’ll collaborate with colleagues from varied backgrounds and experiences, fostering an environment where cross-functional learning, networking, and collaboration are at the core of what we do.Here, we’re not just supporting a law firm; we’re partnering with attorneys and clients to deliver cutting-edge solutions in high-stakes litigation and dispute resolution, world-class regulatory compliance and advisory services, and complex transactions. Our commitment to integrity, ingenuity, agility, and ambition drives us, and we’re proud to have been recognised as the “Best Business Team” by The American Lawyer.This is your opportunity to grow professionally in a dynamic, global environment, surrounded by forward-thinking peers.The Research Services Manager leads the firm’s research function, ensuring attorneys and business professionals receive timely, accurate, and actionable information to support client matters and firm initiatives. This role provides daily supervision, guidance, and support to the Research Analyst team as direct reports, including workload coordination, prioritization, coaching, and quality oversight. The role also partners with Practice Group leaders and the Knowledge Management function (as applicable), and drives adoption of research tools, standards, and training across the firm.What You Will Do:Oversee daily research services delivery (legal, business, industry, news, docket/case, legislative/regulatory, litigation analytics, and public records research) in support of attorneys and business professionals.Provide daily supervision, guidance, and support to the Research Analyst team, including workload coordination, prioritization, coaching, and quality review.Establish service standards, intake/triage workflows, and escalation protocols to ensure responsiveness, quality, and consistency.Consult with attorneys to clarify research objectives, scope, and deadlines; synthesize findings into concise deliverables (emails, briefings, research memos, alerts, and presentations).Partner with Knowledge Management, Practice Management, Business Development/Marketing, and IT to align tools and content with practice needs.Coordinate with the Sr. Manager of Contracts and Licensing and the Director of Research Services on subscription needs assessments, trials, licensing, contract negotiation support, renewals, cost optimization, and usage tracking.Develop and maintain research guides, templates, and internal documentation; promote self-service where appropriate while preserving white-glove support for complex requests.Monitor trends in legal and competitive intelligence and recommend new tools, data sources, and process improvements.Create and report metrics and insights (volume, turnaround time, satisfaction, complexity, and cost) to inform resourcing and strategy.Support incident response and continuity planning for research services (coverage models, vendor outages, and after-hours needs as required).Who You Are:Bachelor’s degree required; Master of Library and Information Science (MLIS/MLS) or equivalent advanced degree strongly preferred.7+ years of progressively responsible legal research experience, including experience in a large law firm, corporate legal department, or professional services environment.2+ years of people management experience (or demonstrated ability to lead teams, projects, and service delivery).Demonstrated expertise with key legal and business research platforms (e.g., Westlaw, Lexis, Bloomberg Law, PACER, SEC/EDGAR, D&B/Capital IQ, Factiva/News platforms), and comfort learning new tools.Strong written and verbal communication skills, with the ability to translate complex findings into clear, practical guidance.Excellent analytical skills, attention to detail, and sound judgment regarding source reliability and completeness.Ability to manage multiple priorities in a deadline-driven environment while maintaining high-quality output.High degree of discretion and professionalism; ability to handle confidential and sensitive information.Client service mindset and responsiveness.Research strategy and source evaluation.#LI-JM1Benefits and MoreAt Goodwin, you will discover your next career opportunity with a rewarding compensation package and comprehensive benefits, including:Health, dental, and vision insuranceLife and disability insuranceRetirement & Savings PlanEmergency back-up child and adult carePaid vacation, sick time off, and holidaysProfessional development and career advancement opportunitiesEmployee recognition and reward programsEmployee wellness and assistance programsEmployee discounts and perksThis position is eligible for overtime: NoThe target salary range for this position varies by location and is commensurate with relevant experience: Boston $103,700 - $155,600 | Los Angeles $111,500 - $167,300 | New York $111,500 - $167,300 | Orange County $111,500 - $167,300 | Philadelphia $101,600 - $152,500 | San Diego $111,500 - $167,300 | San Francisco $119,300 - $178,900 | Santa Monica $111,500 - $167,300SummaryLocation: Boston; Orange County; New York; Santa Monica; Washington DC; Silicon Valley; Los Angeles; San Diego; San Francisco; PhiladelphiaType: Full time
$103.7k - $155.6k
...resolution, world-class regulatory compliance and advisory services, and complex transactions. Our commitment to integrity,... ...global environment, surrounded by forward-thinking peers.The Research Services Manager leads the firm’s research function, ensuring attorneys and...SuggestedFull timeContract work- DescriptionThe Air Quality and Noise Department Manager is responsible for the managerial direction and leadership of a department within... ..., dedication, integrity, safety and overall outstanding service.Provide leadership to the team; direct and coordinate work assignments...SuggestedWork at office
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...Clinical Operations /Full-Time /HybridThe Senior Clinical Trial Manager will be responsible for managing operational aspects of... ...early-phase oncology studies. This includes oversight of contract research organizations (CROs), vendors, and clinical sites across both U...SuggestedFull timeContract workSummer workRelocationRelocation package- ...Contribute to a positive, collaborative, and continuous-improvement-focused team culture.· Perform additional duties as assigned by manager.Requirements:· BS/MS/Ph.D in Analytical Chemistry, Chemistry, Biochemistry, Molecular Biology, or a related scientific discipline.·...Suggested
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...leadership role offers the chance to shape the future of sensor research, work with cutting-edge science, and drive meaningful impact on... ...fluid, ensuring sound scientific and experimental rigor.Manage, mentor, and develop a high-performing team of sensor scientists...- ...and business skills in the above-mentioned fields. Actively reach out to prospective customers, explore business opportunities, manage negotiations and secure contracts. Attend trade shows/relevant conferences. Support the Marketing Team in branding and...Full timeTemporary work
$36.31 per hour
...AST Department: TEMPORARY EMPLOYMENT SERVICES Hiring Pay Scale $36.31 per hour Worksite... ...#TP139440 Assistant Clinical Research Coordinator Filing Deadline: Sun... ...CRC may: provide training, data and chart management, quality assurance check for studies, provide...Hourly payContract workTemporary workLocal areaMonday to FridayAfternoon shift$36.31 per hour
...Assistant Clinical Research Coordinator - TP139440 Position available through UCSD Temporary Employment Services (TES). Employment through TES is an excellent way to gain valuable... ...may provide training, data and chart management, quality assurance check for studies,...Temporary workMonday to FridayAfternoon shift- Kaiser Permanente in San Diego seeks a clinical research associate to collect data for trials, prepare and submit study documentation to IRB/regulatory bodies, and support related lab operations. You will document activities with precision and assist with budget components...
$75k - $90k
...Biolinq is a venture-backed digital health company developing a wearable biosensor platform that measures biomarkers important to the management of many clinical conditions including diabetes. This dynamic role is a part of a team of engineers and scientists developing a...Work at officeLocal areaRemote workFlexible hours$110k - $140k
...analytical challenges, and deliver high-quality data to support research, process development, and regulatory submissions. The... ...oral formats. ~ Strong problem-solving skills and ability to manage multiple projects in a fast-paced environment. Preferred Qualifications...Full time- Position Summary Odyssey is looking for a Clinical Research Coordinator to coordinate and assure the integrity of all activities associated... ...research participants, staff, regulatory affairs and data management groups, laboratory and clinical investigators, management and...Contract workTemporary workWork at officeLocal areaRemote workFlexible hoursWeekend workAfternoon shift
$131k - $163.6k
...fast-paced environment. Key responsibilities include: Leading study execution across startup, enrollment, conduct, and closeout Managing cross-functional teams and external vendors Owning timelines, budgets, study plans, and operational deliverables Supporting...3 days per week- At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities... ...edge technology and exceptional support services to broaden outreach and participation.... .... The Clinical Research Coordinator I manages study conduct from planning through...Full timeWork at officeLocal areaRemote work
- ...participation in Out of Specification investigations and the documentation of analytical deviations along with Qualified Investigators and management Understand and apply ICH and FDA guidance Basic Qualifications: BS in Biology, Chemistry and/or related science...Local areaFlexible hours
- University of California - San Diego Medical Centers in the Department of Medicine seeks a Research Coordinator to coordinate and manage clinical trials, including protocol management, screening for eligibility, data collection and analysis. You will ensure protocol compliance...
- ...close-out of complex Phase I oncology trials. Ensure trial activities comply with protocols, SOPs, GCP, and applicable regulations. Manage and oversee CROs, central labs, biometrics, safety vendors, eTMF providers, and other external partners. Manage, mentor, and...
- Clinical Research Coordinator (CRC) We are seeking a highly organized and motivated CRC to join our research team. The CRC will coordinate and support all aspects of clinical trials and research studies, including subject recruitment, data collection, regulatory compliance...Work at office
$60k - $85k
...may include: laboratory toxicity testing; environmental data management and summaries; QA/QC; statistical calculations; report preparation... ...a range of engineering, science, and technical consulting services. Our range of expertise, project types, and culture make us the...Full timeWork at officeImmediate startFlexible hours$120k - $150k
...Description: The Sr./Clinical Trials Manager (CTM) will support the conduct of clinical... ...functional trial team, and, externally with service providers, investigational site... ...investigational sites with input from Clinical Research and vendors. Identify potential trial...Work at officeLocal area- DescriptionJob Summary:This managing level employee is primarily responsible for developing and providing recommendations on avoiding financial... ...needs or requirements are met.Designs and develops actuarial research by designing complex methods to advance standards, assumptions,...Work experience placement
$71k - $91.85k
...Job Summary: Collects data for clinical trials research, independently. Prepares and/or supports the submission of study documentation... ...measures and documents feedback to research staff and management. Supports and develops materials for the education of research...Full timeTemporary workFor contractorsWork experience placementFor subcontractorLocal areaFlexible hoursShift work- Clinical Trial Manager / Senior Clinical Trial Manager We are partnering with a growing, clinical-stage biotechnology company focused... ...related discipline; advanced degree preferred 5+ years of clinical research experience within the pharmaceutical, biotechnology, or CRO...
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