Clinical Research

• Design clinical studies and evidence strategies supporting global regulatory submissions
• Act as a scientific and clinical liaison with regulatory bodies and external sites
• Partner cross-functionally with R&D, Regulatory, Medical Affairs, Quality, and Commercial teams
• Author and review clinical and regulatory documentation to support product clearance and commercialization
• Build strong internal and external collaborations and mentor junior scientists

Principal Clinical Scientist

• Conduct comprehensive baseline nutrition assessments consistent with study protocols.
• Provide individualized nutrition counseling and lifestyle coaching during scheduled onsite and Telehealth study visits.
• Deliver evidence-based education related to: GLP-1 medications, Weight management strategies, Calorie intake and macronutrient balance, Protein and hydration needs, Sustainable behavior change, Physical activity recommendations.
• Review participant food logs, weight trends, and other study-related data prior to visits.
• Accurately document all participant encounters according to study requirements.
• Collaborate with the clinical research team to ensure protocol compliance.
• Maintain participant confidentiality and adhere to all study documentation and regulatory requirements.

Registered Dietitian – Clinical Research Role

Registered Dietitian – Clinical Research

• Conduct comprehensive baseline nutrition assessments consistent with study protocols.
• Provide individualized nutrition counseling and lifestyle coaching during scheduled onsite and Telehealth study visits.
• Deliver evidence-based education related to: GLP-1 medications, weight management strategies, calorie intake and macronutrient balance, protein and hydration needs, sustainable behavior change, physical activity recommendations.
• Review participant food logs, weight trends, and other study-related data prior to visits.
• Accurately document all participant encounters according to study requirements.
• Collaborate with the clinical research team to ensure protocol compliance.
• Maintain participant confidentiality and adhere to all study documentation and regulatory requirements.

• In collaboration with other members of the clinical research site team works to ensure the execution of assigned studies.
• Responsibilities may include but are not limited to:
• - Screening of patients for study enrollment;
• - Patient consents;
• - Patient follow-up visits;
• - Documenting in source clinic charts;
• - Entering data in EDC and answering queries;
• - Obtaining vital signs and ECGs;
• - May perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up;
• - Requesting and tracking medical record requests;
• - Updating and maintaining logs, chart filings;
• - Maintaining & ordering study specific supplies;
• - Scheduling subjects for study visits and conducts appointment reminders;
• - Building/updating source as needed;
• - Conducting monitoring visits and resolves issues as needed in a timely manner;
• - Ensuring study related reports and patient results are reviewed by investigator in a timely manner;
• - Filing SAE/Deviation reports to Sponsor and IRB as needed;
• - Documenting and reporting adverse events;
• - Reporting non-compliance to appropriate staff in a timely manner;
• - Maintaining positive and effective communication with clients and team members;
• - Always practicing ALCOAC principles with all documentation;
• - Complete all needed activities for study start-up, including completing required training, uploading / printing certificates to file in ISF, etc.;
• - Prepare and attend site initiation visits (SIV’s) and Investigator Meetings (IMs), as needed;
• - Handles all IRB functions for assigned studies independently, and/or with assigned regulatory team member, as needed;
• - Assist with training of new research assistants and coordinators;
• - Assist with scheduling and planning for visit capacity for assigned studies;
• - May set up, train and maintain all technology needed for studies;
• - May assist with study recruitment, patient enrollment, and tracking as needed;
• - May handle more complex study assignments and volumes;
• - May participate in community outreach/education events;
• - Maintaining confidentiality of patients, customers and company information, and;
• - Performing all other duties as requested or assigned.

Travel Clinical Research Coordinator

• Ability to phone screen patients or caregivers in caring and empathetic manner.
• Document patient information correctly in the computer database.
• Schedule/reschedule patient screen and prescreen appointments.
• Manage incoming calls from patients interested in taking part in research studies.
• Evaluate eligibility of potential subjects through methods such as screening interviews, reviews of medical records, or discussions with site clinic staff.
• Learn and maintain knowledge regarding clinical research studies including inclusion and exclusion criteria for different studies.
• Record contact status of patients and document information in the database.
• Review, call and update sponsor patient portals as needed.
• Perform all other duties that may be requested or assigned.

Clinical Research Patient Recruiter

• Partner with VP, Strategic Operations to align training with enterprise priorities and KPIs, translating strategic goals into scalable training programs
• Support workforce planning, capability building, and operational standardization
• Develop and execute a network-wide training strategy and program development
• Create standardized onboarding and role-based training for site staff (CRCs, investigators, site managers, etc.). Design curricula for:
• GCP, ICH guidelines, and compliance
• Protocol execution and study conduct
• Source documentation (ALCOA+)
• Regulatory documentation and inspection readiness
• E/SAE reporting and patient safety
• Partner with Site Operations to identify performance gaps and deploy targeted training
• Improve site KPIs (enrollment, retention, protocol adherence, data quality)
• Drive consistency and reduce variability across sites
• Ensure training meets FDA, ICH-GCP, and sponsor requirements
• Maintain inspection-ready training documentation
• Support audits, inspections, and CAPA implementation
• Manage and optimize LMS for training compliance and tracking
• Implement scalable learning solutions (e-learning, virtual, microlearning)
• Support adoption of clinical technologies (CTMS, EDC, eReg) through training
• Lead and develop training personnel or site-based trainers
• Influence site leaders to adopt standardized training practices
• Promote a culture of continuous learning and quality
• Establish and track training KPIs (compliance, time-to-productivity, audit outcomes)
• Analyze data to improve training effectiveness and operational impact
• Provide regular reporting to VP, Strategic Operations
• Lead training for new SOPs, systems, and process changes
• Support growth, scalability, and decentralized trial models
• Drive adoption of standardized practices across a distributed network
• Routinely assess study-specific process and training compliance and identifies emerging risks.
• May develop and support execution of corrective action plans at site and study level.
• Oversee people management activities including interviewing and selection, performance appraisals, job description preparation, employee counseling, and career coaching. Oversee payroll timecards, absence tracking/approvals, onboarding, and team training per operational needs.
• Participate, lead and/or present in management, training, department, site, and other meetings.
• Maintain strict confidentiality of employee, participant, customer, executive, board, business, and company information at all times, using sound judgment when handling sensitive or time-sensitive matters.
• Perform other duties, responsibilities, and special assignments as requested or assigned in support of business needs.

Senior Manager, Training & Development – Clinical Research

• Leading, planning, executing, managing, and oversight of clinical studies according to research ethics guidelines, ISO standards, internal SOPs, applicable regulations, and portfolio priorities.
• Leads the implementation of clinical protocols, informed consent forms, and study-related materials for clinical studies.
• Manages site initiation activities (e.g., study start-up documentation preparation).
• Responsible for IRB communication, including document preparation and submission of Arthrex study initiatives.
• Implementing modifications to optimize protocol results or edit/amend study documentation if necessary.
• Collaborate with Data Management team to ensure the electronic data capture system (EDC) is designed to collect all required data per the protocol.
• Responsible for training internal staff assigned to studies.
• Project lead for other research staff assigned to multicenter studies.
• Key decision maker for study amendments and strategies.
• Maintain appropriate monitoring and maintenance of clinical sites to ensure the overall successful conduct of assigned clinical studies.
• Oversee all aspects of the assigned clinical projects, including essential documents, electronic data collection, change management, risk management, and monitoring activities.
• Set-up and maintain accurate progress and Site study status tracking logs to provide reports and updates of assigned clinical research projects.
• Oversee follow-up and lead query resolution with sites via ongoing interactions.
• Participation in investigator meetings, Site initiation, monitoring, and close-out visits when applicable.
• Complete central, remote, and on-site monitoring reports and follow-up letters.
• Complete monitoring report reviews of other staff.
• Oversee monitoring activities for the assigned projects and is responsible for ensuring actions are taken when applicable.
• Identify and mitigate quality risk and/or issues associated with assigned studies/activities.
• Facilitate appropriate documentation to maintain compliance with the Finance and Compliance departments.
• Prepare and track clinical study budgets that include both sponsor costs and sites costs.
• Responsible for the timely completion of deliverables, inclusive of contributing to interim and final study reports.
• Facilitate efficient utilization of available clinical data, addressing the needs of internal and external stakeholders (e.g., publications).
• Works closely with leadership, product management, medical writing, project manager, and other research staff to manage assigned studies.
• Conducts regular investigator meetings to ensure protocol compliance and site engagement.
• Actively participate in research committees, study groups, and cross-functional portfolio governance activities to support continuous improvement and strategic alignment.
• Engage in and support departmental initiatives and cross-functional team projects, collaborating by driving execution, problem-solving, and achievement of key business outcomes.
• Conducts project huddles and able to lead cross-functional projects.
• Mentoring and training staff.
• Serve as a cross-functional lead within an assigned study and product portfolio, ensuring alignment across Clinical Operations, Product Management, Data Management, Regulatory, Compliance, and other key stakeholders.

Senior Clinical Study Manager

• Lead end-to-end analytics initiatives from problem framing and experimental design through production delivery
• Architect and implement scalable data solutions
• Fuse disparate data sources and establish data preparation standards
• Implement data quality controls and manage schema changes
• Develop, evaluate, and deploy predictive models and optimization approaches
• Support text-heavy and unstructured-data use cases with NLP methods
• Deliver decision-support products through Power BI
• Provide technical leadership and consultation

Biostatistician

• Acquire, integrate, and prepare data from multiple sources to enable operational reporting, readiness analytics, and decision support.
• Design and implement ETL/ELT pipelines using SQL Server and Databricks leveraging Apache Spark (PySpark) for scalable batch processing and data transformation.
• Develop and maintain curated, analysis-ready datasets (e.g., dimensional models, governed reporting tables) with attention to data quality, lineage, and repeatability.
• Optimize data processing performance (partitioning strategies, efficient joins, job tuning) and contribute to reliable scheduling/orchestration and monitoring of recurring workloads.
• Apply statistical methods, data mining, and machine learning to generate actionable insights, forecasts, and predictive analytics relevant to military missions and readiness.
• Create dashboards and analytical products using Power BI, including semantic modeling and measures to support consistent metrics and reporting.
• Support low-code solutions by integrating data products into Power Apps (Canvas and Model-Driven) and automations using Power Automate.
• Contribute to text and language-focused use cases by preparing and analyzing unstructured data (basic NLP preprocessing, labeling/curation, feature creation).
• Demonstrate familiarity with LLMs and agent concepts (prompting patterns, retrieval-style workflows, evaluation considerations) and assist senior team members in implementing these capabilities where appropriate.
• Document data sources, transformations, assumptions, and analytical methodologies to ensure transparency and operational continuity.

Junior Biostatistician

• publish content on external website (dcri.org) and intranet (Pulse) using content management systems (Drupal and SharePoint, respectively)
• create graphics for social media, external websites, and intranet
• determine requirements for instructional audiovisual media and coordinate production of slide series, films, videotapes and other media materials for use
• works both independently and collaboratively with internal Shared Services department, Production Designers and Marketing Managers on a wide mix of creative initiatives
• manage calendar of DCRI’s scientific conferences, researching Duke-related presentations at each show
• for scientific conferences at which DCRI has an exhibit booth, coordinate the marketing collateral needed for the booth
• prepares layouts, designs, artwork and formats for use in publication and/or exhibition design
• contribute to editorial planning by suggesting content ideas, target channels and audiences, and appropriate project timelines
• compile weekly internal newsletter in MS Outlook
• create quarterly external-facing newsletters using Constant Contact
• occasional content development for DCRI-owned external and internal channels
• serve as backup manager of DCRI’s social media channels (Twitter and LinkedIn)
• assist in the shooting and production of video and audio projects
• develop a broad knowledge of research conducted at the DCRI

Clinical Research Comm Specialist III

• Accountable for the full spectrum of investigator engagement from identification and qualification through enrollment, and support database lock, and study closeout
• Serve as a clinical trial scientific ambassador, ensuring investigators deeply understand protocol intent, scientific rationale, and patient eligibility requirements
• Develop and sustain strategic, high-trust relationships with investigators that span trials and therapeutic areas
• Influence enrollment by co-creating tailored recruitment strategies aligned with site capabilities, patient population realities, and study objectives
• Proactively find opportunities to reach new patients, accelerate enrollment and increase impact at priority sites
• Capture and elevate critical insights from sites to optimize feasibility, protocol design, and study conduct
• Lead site-level strategy and risk planning to ensure strong and predictable enrollment and data delivery
• Collaborate across functions and with vendor partners to resolve operational barriers
• Maintain advanced understanding of local treatment paradigms and standard of care to influence strategic country/site selection and protocol localization

Clinical Trial Liaison – Clinical Research Lead

• Accountable for the full spectrum of investigator engagement from identification and qualification through enrollment, and support database lock, and study closeout
• Serve as a clinical trial scientific ambassador, ensuring investigators deeply understand protocol intent, scientific rationale, and patient eligibility requirements
• Develop and sustain strategic, high-trust relationships with investigators that span trials and therapeutic areas
• Influence enrollment by co-creating tailored recruitment strategies aligned with site capabilities, patient population realities, and study objectives
• Proactively find opportunities to reach new patients, accelerate enrollment and increase impact at priority sites, including for example, novel site models, community-based research initiatives etc
• Capture and elevate critical insights from sites to optimize feasibility, protocol design, and study conduct
• Lead site-level strategy and risk planning to ensure strong and predictable enrollment and data delivery
• Leverage performance metrics to anticipate issues, intervene decisively, and maintain momentum toward clinical milestones
• Drive inspection readiness as a continuous discipline across sites
• Collaborate across functions and with vendor partners to resolve operational barriers, ensuring delivery with speed and quality
• Maintain advanced understanding of local treatment paradigms and standard of care to influence strategic country/site selection and protocol localization
• Provide oversight and quality assurance for vendor monitoring, escalating risks proactively
• Cultivate a portfolio of strategically aligned, high-impact investigators who consistently prioritize client trials
• Enable an exceptional investigator experience by being a responsive, knowledgeable, and valued scientific partner
• Collaborate cross-functionally (e.g., Medical, Clinical, Study Delivery) to align on trial and site priorities, troubleshooting challenges with urgency and creativity
• Conduct data-informed site prospecting and prioritization, contributing to trial competitiveness and regional strategic execution
• Maintain scientific fluency and therapeutic expertise to lead meaningful, solutions-focused discussions with site personnel
• Act as a key liaison between field teams, vendors, and investigators, ensuring alignment, shared purpose, and continuous knowledge transfer
• Partner closely with field team colleagues to elevate the investigator and site experience, ensuring seamless collaboration and improving enrollment outcomes and Investigator relationships

• In collaboration with other members of the clinical research site team, works to support source document requirements for assigned studies.
• Creation of source documents that will follow GCP Guidelines and 21 CFR Part 11 Compliance in addition to internal SOPs.
• Create templates, worksheets, supplemental source for visits based on detailed review of protocol-defined exams, tests, evaluations, and assessments.
• Initial creation of source documents will use all available protocol specific documents (i.e., current IRB approved protocol, blank or annotated CRF, Sponsor provided source templates/worksheets, or reference manuals) to create a source document that is accurate and complete and to ensure that the source document is equipped to record all the required data for the visit.
• Creating, maintaining, updating, control, and release source documents, including paper and electronic source documents in line with the study protocol, and relevant sponsor guiding documents.
• Reviewing draft source and ensuring it is accurate and complete and to ensure that the source document is equipped to record all the required data for the trial.
• Coordinating initial source review and update process.
• Filing, maintaining, distributing, organizing, and archiving source documents for each clinical trial.
• Updating current source documents according to new clinical study protocol amendments.
• Activating studies and visits at the appropriate time.
• Supporting Quality Control (QC) of source documents before it goes to the users.
• Attending all relevant meetings to stay up to date with upcoming studies, progress on current studies, and studies closing out.
• Maintaining a single tracker for the department to track source document design activities and the status of the activities.
• Maintaining version control of all source documents.
• Managing daily communication with site staff and other internal departments.
• Remaining up to date with all assigned Clinical Study Protocol for study.
• Developing and maintaining excellent working relationships with internal and external clients to understand and meet their needs in line with company policies and procedures.
• Maintaining a positive, results-oriented work environment, building partnerships within the team and across the organization at large, and modeling teamwork.
• Participating in continuing education activities to maintain current knowledge of source document design and relevant software.
• Performing all other duties that may be requested or assigned.

Clinical Research Source Development Coordinator

• Serve as a member of the central services team to deliver pharmaceutical support.
• Ensure delivery of therapeutic medication monitoring, EMR regimen build and review, protocol management.
• Provide drug information, dosing, monitoring, and education for safe medication therapy for patients in clinical trials.
• Collaborate with Research Department staff for quality patient care.
• Perform administrative and communication responsibilities for clinical trials.
• Support the development of new research regimen builds and inquiries.

Oncology Clinical Research Pharmacist

• Leads Life Extension Clinical Research and ensures studies are conducted in a timely, quality driven manner while following all applicable guidelines
• Provides overall leadership to LECR and staff by clearly communicating goals and expectations and driving productivity with a sense of urgency while ensuring 100% compliance with rules and regulations.
• Ensure all clinical trial projects (internal and external), to include project management, tracking and reporting trial progress and monitoring test item expiration dates in relation to project timelines
• Management and oversight of research projects and laboratory components of studies; develops appropriate study design and establishes accurate timelines; collaborates on statistical plans and data analysis
• Prepares and/or supervises the preparation of the Protocol, Informed Consent and associated documentation for clinical studies and assures necessary project approvals from an Institutional Review Board (IRB) are obtained
• Primary point of contact for the IRB
• Prepares and manages all LE Clinical Research budgets
• Sets priorities for all staff to assure project timelines are met, including active promotion of clinical research initiatives, i.e. use of social media
• Assures all applicable regulations are implemented and followed; supervises management of data files and confidential information; follows established SOPs, i.e. for appropriate document destruction
• Responds to inquiries from individuals seeking funding or product donations, and if warranted, presents project and recommendations to administration
• Monitors progress of ongoing external projects that received Life Extension support and/or donated materials, assuring resupply so materials do not expire without replacement during a project
• Seeks out ways to employ innovative technology to optimize organization and individual efficiency and performance
• Proactively drives the effort to achieve the goal of creating an impactful Clinical Center of Excellence.

Director, Clinical Research

• Full accountability for country-level study delivery and performance
• Serve as the client’s voice within Civia, ensuring their priorities, timelines, and standards are understood and met across all functions
• Maintain disciplined oversight of start-up, recruitment, regulatory progress, data quality, and site performance
• Drive immediate cross-functional action when performance deviates from plan
• Lead structured governance routines with clarity, transparency, and solution orientation
• Ensure ongoing audit and inspection readiness across all study activities

Clinical Trial Manager

• Responsible for study coordination and data management with a focus on managing subject recruitment and enrollment
• Maintain site compliance for all clinical trial activities and regulations
• Complete all relevant Profound Research required training in a timely manner
• Educates and directs protocol compliance with physicians and staff
• Ensure good documentation practices are applied by all team members
• Communicate effectively and professionally with coworkers, leadership, study subjects, sponsors, CROs, and vendors
• Acts as a patient advocate
• Collaborates with scheduling staff and the physician to assure appointments are scheduled correctly and treatment orders are written and delivered

Clinical Research Coordinator, RN

• Responsible for the performance of the research study under the medical supervision of the Principal Investigator and the research director
• Overall successful implementation and ongoing site management of the research studies
• Provide coverage in clinics when research staff are out of the office
• Precept new research staff in clinics
• Assist with research projects assigned by the Senior Clinical Research Coordinator III

Clinical Research jobs in Florida

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Principal Clinical Scientist

Registered Dietitian – Clinical Research Role

Registered Dietitian – Clinical Research

Registered Dietitian – Clinical Research

Travel Clinical Research Coordinator

Clinical Research Patient Recruiter

Senior Manager, Training & Development – Clinical Research

Senior Clinical Study Manager

Biostatistician

Junior Biostatistician

Clinical Research Comm Specialist III

Clinical Trial Liaison – Clinical Research Lead

Clinical Trial Liaison – Clinical Research Lead

Clinical Research Source Development Coordinator

Oncology Clinical Research Pharmacist

Director, Clinical Research

Clinical Trial Manager

Clinical Research Coordinator, RN

RN Clinical Research Coordinator III – Drug Development Unit