1,216 Results for

Clinical Research Manager Jobs in Florida

Jobs

Gainesville, FL11 days ago

$88,670.40–$151,590.40

Motor Vehicle Operator Designation: Employees in this position: Will not operate vehicles for an assigned business purpose NOTE: A frequent driver is defined as one who uses his/her personal or Shands automobile a) at least once daily, b) at least five individual trips per week or c) drives, on average, over 150 miles per week in the performance of his/her job. Accountable for daily staffing and unit based follow-up of issues that assist in the assessment, planning, implementation and evaluation of patient care needs based on quality benchmarking, patient acuity/care trends, staff clinical education needs and patient satisfaction.

Atlantis, FL18 days ago

Additional options for dental and vision benefits, life and disability coverage, flexible spending accounts, supplemental health protection plans (accident, critical illness, hospital indemnity), auto and home insurance, identity theft protection, legal counseling, long-term care coverage, moving assistance, pet insurance and more. HCA Healthcare is an advanced healthcare network that has committed up to $300 million to our incredible team members over the course of three years.

Hollywood, FL30 days ago

Part-time

We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success. Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in-patient capability.

Hollywood, Florida30 days ago

Miami, FL29 days ago

Leads efficient clinical research nursing team meetings; assures effective communications; provides leadership in problem solving logistical challenges to assure study objectives are achieved according to protocol and projected timeline. Collaborates synchronization of study visits, procedures, and clinical tests with data collection schedules, established time-points; effectively advances study participants through protocol; expedites overall study progression with minimal clinical disruption.

New!

Brandon, Florida6 days ago

This role serves as the primary on-site leader of the research team, partnering closely with physicians, clinical staff, and national research leadership to build and manage a high-performing research program that advances innovation in cardiovascular medicine. This role requires a proactive leader who can champion research within the practice, mentor staff, implement scalable processes, and advocate for research growth among physician partners and operational leadership.

Hollywood, FL10 days ago

Part-time

GCP, and ICH guidelines; Able to take a flexible approach to shifting priorities; Able to manage multiple projects and responsibilities; Motivated to work consistently in a fast paced and rapidly changing environment; Must be detail oriented and have exceptional computer, organizational, and communication skills – both written and oral. Performs ongoing review of a percentage sampling of study inclusion/exclusion, study procedure records, and laboratory reports to ensure that they are conducted according to the protocol, applicable SOPs, ICH/GCP guidelines and federal regulations.

Tampa, FL30+ days ago

alternative to the number of years of direct experience required, not to exceed: (a) Two years of direct experience for an associate degree; (b) Four years of direct experience for a bachelors degree; (c) Six years of direct experience for a masters degree; (d) Seven years of direct experience for a professional degree; or. USF is a member of the Association of American Universities (AAU), a group that includes only the top 3% of universities in the U.S. With an all-time high of $738 million in research funding in 2024 and as a top 20 public university for producing U.S. patents, USF uses innovation to transform lives and shape a better future.

New!

Gainesville, FL4 days ago

$46,000–$55,000 Per Year

Job Description:The University of Florida Diabetes Institute (UFDI) is seeking a qualified and enthusiastic individual to coordinate research and patient participation for the Diabetes STEPS program, a statewide program seeking to increase screening for type 1 diabetes throughout the state of Florida. The University of Florida Diabetes Institute (UFDI) is seeking a qualified and enthusiastic individual to coordinate research and patient participation for the Diabetes STEPS program, a statewide program seeking to increase screening for type 1 diabetes throughout the state of Florida.

Tampa, FL30+ days ago

Part-time

Develops budget and ensures financial and operational metrics are meeting organizational objectives by identifying, analyzing, and monitoring issues that affect profitability, growth, and productivity. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology.

miami, FL30+ days ago

Core Qualifications Bachelor's degree in relevant field required Current Research Coordinator certification by the Association of Clinical Research Professionals or Society of Clinical Research Associates for a minimum of 6 months Minimum 4 years of relevant experience required Knowledge, Skills and Attitudes: Skill in collecting, organizing and analyzing data. This role manages multiple studies' daily operations, carries out study coordination duties from protocol development and initiation to study close-out according to regulatory/sponsor guidelines, assures each study's integrity, and mentors less experienced Clinical Research Coordinators.

Gainesville, FL29 days ago

$53,000–$60,000 Per Year

The Clinical Research Coordinator II will work collaboratively with the Vice Chair of Research, Principal Investigators (PIs), the Clinical Research Manager, research administrators, coordinators, sponsors, and institutional partners to ensure all research activities are conducted in accordance with federal regulations, University of Florida policies, and sponsor requirements. This position plays a vital role in coordinating and managing clinical research activities across all phases of study operations, including regulatory submissions, participant recruitment and enrollment, study implementation, data collection, compliance monitoring, reporting, and project closeout.

Miami, FL24 days ago

This role manages multiple studies' daily operations, carries out study coordination duties from protocol development and initiation to study close-out according to regulatory/sponsor guidelines, assures each study's integrity, and mentors less experienced Clinical Research Coordinators. The Clinical Research Coordinator 3 (A) serves as an experienced clinical research professional responsible for providing leadership in the planning, implementing, monitoring, and evaluating of multiple clinical research protocols.

Hollywood, Florida30+ days ago

Tampa, Florida30+ days ago

New!

Tallahassee, FL6 days ago

$50–$55 Per Hour

With interest/expertise in Science 37's decentralized model of care delivery, the Mobile Research Nurse will perform delivery of care to participants as well as collaborate with brick and mortar sites, if indicated, for shared clinical trial implementation. Science 37's Nursing Solutions Group brings together expert nurses who share a passion for organizing, planning and implementing mobile clinical nurse services to participants in clinical trials.

Lake Worth, FL30+ days ago

As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Join a leading, integrated clinical research network dedicated to high-quality data, patient-centered care, and innovation in clinical trials.

miami, FL30+ days ago

The incumbent works closely with study team members and other staff/faculty/study sites to ensure study participant safety and adherence to approved protocols, help with study-related administrative tasks, facilitate across-the-board flow of information, and coordinate study activities and personnel. Assures synchronization of study visits/procedures/ clinical tests with data collection schedules, established time-points; manages progress of study participants through protocol; expedites overall study progression.

Gainesville, FL10 days ago

$53,000–$65,000 Per Year

Experience working with databases and/or subject data; Proficiency with Microsoft Office suite, particularly Outlook, Excel, Word; Strong interpersonal skills, as well as the ability to work with a broad range of people including investigators, physicians, clinic and hospital staff, sponsors, partners at other institutions. Attends Investigator meetings and represents the University of Florida in a professional manner; Follows each subject's clinical course during inpatient hospitalizations and at clinic visits, confirming that all protocol-specific tests and procedures are completed within study timelines.

Tampa, FL22 days ago

TGH Main Campus'',''1 Tampa General Circle'','' '',''Tampa'',''33601'',''On Site'',''On Site'',''Clinical Research'',''Clinical Research'',''Florida Health Sciences Center Tampa General Hospital'',''Florida Health Sciences Center Tampa General Hospital'',''Per Diem/Pool'',''Per Diem/Pool'','''','''',''Night Job'',''Night Job'','''','''',''On Site'',''On Site'','''','''','''','''',''Varies'',''Varies'',''22.32'',''22.32'',''May 21, 2026, 3:50:22 PM'',''May 21, 2026, 3:50:22 PM'',''false'',''679361'',''679361'',''true'',''679361'',''false'',''Submission for the position: Pool Clinical Research Assistant - (Job Number: 260001WV)'',''false'',''679361'',''false'',''true''. ''679361'',''true'',''679361'',''false'',''Submission for the position: Pool Clinical Research Assistant - (Job Number: 260001WV)'',''false'',''679361'',''false'',''true'',''Pool Clinical Research Assistant'',''260001WV'',''!*!

New!

Gainesville, FL4 days ago

$70,000–$73,500 Per Year

This position maintains system functionality, monitors billables, creates study budgets, and supports system integration and user training. The role requires strong analytical, technical, and financial skills to ensure accuracy, efficiency, and compliance across clinical research operations.

New!

ORLANDO, Florida6 days ago

Essential Functions· Participate in the coordination of multi-site or large-scale clinical trials research studies conducted by a supervising principal investigator(s) in support of activities that meet objectives of assigned research protocol(s).· Shift: Day / Full Time Location: Orlando Title: Clinical Research Coordinator I Summary: Participate in the development, coordination and implementation of research and administrative strategies essential to the management of clinical trials research.

Delray Beach, Florida23 days ago

Please contact Ashley Sin at (303) 317-5486 x486 or at ashley.sin@emvenio.com today to learn more about our opportunities where you can make a difference in your own career! Two (2) years' experience in starting and performing Phlebotomy/Peripheral Blood Draw, IVs, and Subcutaneous Injections (date of last practice within 6 months, preferred) .

Miami, FL30+ days ago

BSN - Bachelors of Science in Nursing • RN Licensure within the State of Florida or Multi-State Enhanced Nursing License Compact (eNLC) - maintain active and in good standing throughout employment • IATA certification completion required within 3 months of hire date • American Heart Association ACLS (Advanced Cardiovascular Life Support) certification required within 2 months of hire • American Heart Association PALS (Pediatric Advanced Life Support) certification completion required within 6 months of hire • American Heart Association BLS - maintain active and in good standing throughout employment • 2-4 years of professional research or healthcare experience • 1-3 years of Phase 1 clinical research experience • ARNP highly preferred • Clinical research certification (e.g., CCRC, CCRP, CRA) preferred • Bilingual in English/Spanish preferred • Pediatric Nursing experience in an acute care setting preferred • Experience in neurology, neurosurgery, or oncology preferred • Experienced with database management tools and/or REDCap preferred • In-depth knowledge of Phase I clinical trials • Demonstrated knowledge of clinical research trial design and execution • Experienced with electronic medical record and clinical trial management software applications • Strong written and verbal communication skills • Excellent interpersonal skills • Excellent problem-solving skills • Effective organizational and project management skills • Ability to pay close attention to detail • Ability to comprehend professional and scientific journals • Ability to apply principles of logical and scientific thinking to a wide variety of intellectual and practical problems • Ability to establish and maintain effective working relationships with coworkers, managers and clients • Proficiency in Microsoft Office including Access, Word, Excel, Outlook, and PowerPoint • Willing to work off-hours depending on the study requirements. This research position reports directly to the NCH-RI Clinical Trials Office (CTO) Manager but works closely with Lead CRAs, Study Team (PI, Sub-Is, CRC, etc.), NCH-RI departments and Nicklaus Childrens Hospital (NCH) department administrators, and other clinical research professionals to help ensure that clinical research and related activities are performed in accordance with all applicable Federal regulations, NCH/NCH-RI applicable policies and sponsor policies/requirements.

New!

Lake Worth, Florida3 days ago

Miami, FL30+ days ago

$35,600–$60,400 Per Year

Baba ShettyKristen SpensieriChristian DucatDE&IERGsAwardsOur Office LocationsHow We PartnerHow We PartnerAmplifying RecruitmentLink to Syneos OneReinventing the end-to-end modelAccelerating Global DeploymentBroadening the CommercializationDynamic Control RoomAnswersuiteHuman Behavioral insightsKineticPatient Voice ConsortiumInnovating the delivery model for clinical trialsDynamic AssemblyTrusted ProcessSolutionsClinical DevelopmentBioanalytical SolutionsEarly PhasePhase II-IVPhase II-IIIPhase IIIb-IVSite Start upBiostatistics and Statistical ProgrammingClinical Data ManagementClinical MonitoringMedical WritingTrial Master File TMF OperationsInvestigator Management SolutionsReal WorldLate PhaseDecentralized SolutionsSite and Patient AccessFSP 360Medical AffairsCommercial DeliveryDeployment SolutionsEngagement CenterField Sales TeamsSales OperationsMedical Science Liaisons NursesRecruiting and Direct Hire SolutionsLearning SolutionsCommunicationsAdvertisingMedical CommunicationsPatient AdvocacyNaming and Brand IdentityPayer MarketingHealthcare Public RelationsValue & AccessConsultingCommercial Advisory GroupScientific and Medical Affairs Advisory GroupR&D Advisory GroupRisk and Program Management Advisory GroupSyneos OneFull-Service DevelopmentFull-Service commercializationFull-Service REMSRisk-Minimization measuresGlobal Risk Management and REMSNon-Core Asset DevelopmentEstablished Brands CommercializationTherapeutic DepthBiosimilarsCardiovascularCell and Gene TherapyNeuroscienceDermatologyEndocrine and MetabolicGastroenterologyImmunology and InflammationInfectious DiseaseOncology and HematologyOpthalmologyMedical Devices and DiagnosticsPediatricsRare DiseaseRespiratoryWomens HealthInsights Hub InvestorsNewsEventsCareersContact usInvestorsNewsEventsCareers Contact usEnglishEnglishFrançais CanadienEnglishEnglishFrançais CanadienSearch formSearch Medical Assistant - Clinical Research Bilingual EnglishSpanish - Miami FLUpdated YesterdayLocation Miami FL United StatesJob ID 25102495 Not ready to applyJoin our Talent NetworkDescription Medical Assistant - Clinical Research Bilingual EnglishSpanish - Miami FLSyneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. Apply for this jobNot ready to applyJoin our Talent NetworkRecently Viewed JobsTerritory Sales Specialist - 2 minutesBusiness Development Manager - 7 minutesRecommended JobsBusiness Development ManagerBusiness Development ManagerExecutive Director Business Development - Mid MarketExecutive Director Business Development - Mid MarketExecutive Director Business Development - Mid Market Share this jobApplyInside Syneos Health Our Values Who We Are Our Solutions Diversity Equity And Inclusion Why Work HereDiscover what our more than 29000 employees already know work here matters everywhere.

Miami, FL30+ days ago

Visits appropriate referral sources (i.e., hospitals, clinics, etc.) to market clinical studies/trials and conducts face-to-face screenings and assessments to determine eligibility; communicates with family or persons involved in participant's care. Moreover, the Clinical Research Participant Specialist schedules assessments, completes clinical intakes and assessments, conducts in-person and telephone interviews, and markets clinical studies/trials.

New!

Orlando, FL5 days ago

Education/Training: Must meet one of the following: Bachelor's degree in health-related field (i.e., Healthcare Administrative, Nursing, Respiratory Therapy, Health & Wellness or Health Information Management); or Associate degree in related field (i.e., Healthcare Administration, Nursing, Respiratory Therapy, Health & Wellness or Health Information Management) and one (1) year of clinical research or healthcare experience (in addition to the requirements listed in the Experience section); or Graduate of an accredited allied health program and one (1) year of clinical research or healthcare experience (in addition to the requirements listed in the Experience section). Position Summary Department: Clinical Research Coord I Shift: Day / Full Time Location: Orlando Title: Clinical Research Coordinator I Summary: Participate in the development, coordination and implementation of research and administrative strategies essential to the management of clinical trials research.

New!

Florida5 days ago

Follows quality issue processes by escalating systematic or serious quality issues, data privacy breaches, Clinical Study Protocol (CSP) or ICH-GCP compliance issues to Local Management and/or Clinical Quality Management (CQM) as required. The SrCRA is responsible for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies, in compliance with Client Procedural Documents, international guidelines such as ICHGCP, and relevant local regulations and that the sites deliver according to their respective commitment in the individual studies.

New!

Miramar, FL5 days ago

Additional benefits include, but not limited to, Employee Assistance Program, Employee Stock Purchase Plan, Tuition Assistance, Flexible Spending Accounts, Health Savings Account, Life Style Spending Account, Volunteer Time Off, Paid Parental Leave, if eligible , Family Building Benefits, Virtual Physical Therapy, Accident, Critical Illness and Hospital Indemnity Insurances, Identity Theft Protection, Legal Plan, Voluntary Life Insurance and Long Term Disability and more. Provides ongoing assessment of the study subject/patient to identify Adverse Events (AEs), ensures proper documentation and reporting of all AEs, including follow up of open AES when subjects are not in-house, and provides any appropriate clinical care or instructions to subjects, as directed by the PI or as deemed medically necessary by their professional judgment.

Coral Gables, FL30+ days ago

Collaborates with other University groups such as Principal Investigators and study teams, Compliance, IRB (Human Subject Research Office), Risk Management, sponsors and other relevant offices to ensure that sponsored research projects are managed in an efficient and effective manner consistent with UM policies and procedures, and applicable agency guidelines, laws and regulations. Supports the Executive Director and Associate Directors of Pre-Award in developing and delivering staff training on the unique requirements and complexities of corporate/industry funded clinical research and clinical trial projects.

Miami Beach, FL9 days ago

What You'll Do: Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner.

Miami Beach, FL9 days ago

Tampa, FL30+ days ago

Other job duties may include support of therapeutic studies including completion of data entry into various database systems, follow-up of patients according to protocol (via review of records, clinic visit or telephone call), ordering supplies, preparing patient/participant documents for study visits, assisting with the maintenance of regulatory documents, communicating with study sponsors, and facilitating the collection of study-required specimens. These positions work closely with patients, patient families, study sponsors (from smaller pioneer biotech companies through large pharmaceutical companies), and the Clinical Trial Team that includes physicians, pharmacists, nurses, data monitors and data managers.

Sun City Center, FL30+ days ago

n \nhttps://moffitt.org/clinical-trials-research/clinical-trials/clinical-trials-administration \n \nThese positions work closely with patients, patient families, study sponsors (from smaller pioneer biotech companies through large pharmaceutical companies), and the Clinical Trial Team that includes physicians, pharmacists, nurses, data monitors and data managers. \nCredentials and Qualifications: \n\nBachelor's degree with 2 years clinical trials coordination experience\nIn lieu of a bachelor's degree, an associate's degree with 4 years clinical trials coordination experience may be considered\n* CCRP/CCRC certification preferred.

Orlando, FL29 days ago

$31.53–$52.24 Per Hour

Communicates effectively with investigators, scientists, project managers, CRCs, staff, and research participants, serving as a participant advocate by reporting needs, concerns, abnormalities, or adverse events. Conducts clinical research trials by escorting volunteers through study visits, performing clinical tasks, collecting data, and communicating results to the Clinical Research Coordinator (CRC and investigators.

Tampa, FL26 days ago

These positions work closely with patients, patient families, study sponsors (from smaller pioneer biotech companies through large pharmaceutical companies), and the Clinical Trial Team that includes physicians, pharmacists, nurses, data monitors and data managers. Our Clinical Research Coordinators come from a variety of backgrounds and experiences, including social sciences (public health, social work, sociology, psychology, communications, and more), biological sciences, business, and humanities.

Palmetto Bay, FL30+ days ago

Collaborating with department leaders in Business Development, Patient Recruitment, Finance, and Budgets Contracts and Quality to coordinate delivery expectations, meet expected study milestones (such as site activation targets, enrollment targets, etc.), meet budgets, and delivery quality data to sponsors. Overseeing resourcing allocations, site assignments and study team members'' output and performance, to ensure study deliverables are on track, identifying risks to delivery or quality, and escalating any risks to clinical trial management deliverables (timeline, quality and budget).

Palmetto Bay, Florida30+ days ago

Collaborating with department leaders in Business Development, Patient Recruitment, Finance, and Budgets Contracts and Quality to coordinate delivery expectations, meet expected study milestones (such as site activation targets, enrollment targets, etc.), meet budgets, and delivery quality data to sponsors. Overseeing resourcing allocations, site assignments and study team members' output and performance, to ensure study deliverables are on track, identifying risks to delivery or quality, and escalating any risks to clinical trial management deliverables (timeline, quality and budget).

Hollywood, FL30+ days ago

Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. • Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.

Miami, FL30+ days ago

To ensure the highest level of compliance, the University of Miami Sylvester Comprehensive Cancer Center (Sylvester) has in place strong oversight committees, high quality protocols, and training of new investigators and fellows in the development of clinical protocols. UHealth-University of Miami Health System, South Florida's only university-based health system, provides leading-edge patient care powered by the ground breaking research and medical education at the Miller School of Medicine.

New!

Lake Mary, Florida3 days ago

Remote

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. Position Summary: The Clinical Source Development Coordinator is an integral part of the Clinical team and will work closely with the Site teams and other key stakeholders in designing, updating, controlling, and releasing source (electronic or paper) for clinical trials.

Miami, FL25 days ago

Beyond administrative duties, responsibilities of a SCRC may include subject recruitment (screening, consenting support and enrollment), follow-up, data management (entry and reporting), detailed record keeping, regulatory compliance, collection and reviewing study data to enter it into the study and site systems, and correspondence with investigators, IRBs, sponsors, CRO''s and regulatory authorities. Under direction of the Senior Manager of Clinical Trial Operations, the Senior Clinical Research Coordinator, CTO (SCRC) works independently on complex projects/assignments and manages and conducts the day-to-day activities of a research study.

Miami, FL30+ days ago

Beyond administrative duties, responsibilities of a SCRC may include subject recruitment (screening, consenting support and enrollment), follow-up, data management (entry and reporting), detailed record keeping, regulatory compliance, collection and reviewing study data to enter it into the study and site systems, and correspondence with investigators, IRBs, sponsors, CROs and regulatory authorities. Description Under direction of the Senior Manager of Clinical Trial Operations, the Senior Clinical Research Coordinator, CTO (SCRC) works independently on complex projects/assignments and manages and conducts the day-to-day activities of a research study.

Maitland, FL30+ days ago

Essential Job Duties: Ensures the medical well-being and safety of the study participants through the safe performance and ethical execution of the clinical trials, in adherence with FDA, ICH, NIH, GCPs & HIPAA guidelines, study protocols, as well as company policies and processes. Minimum Qualifications: MD or DO degree, an active physician license (in good standing) in the state of practice for this role, and a minimum of 2 years of experience in a medical research environment, or an equivalent combination of education and experience, is required.

New!

Tamarac, Florida3 days ago

With programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. The Clinical Research Assistant is an entry level clinical position and is designed to fully integrate the individual in the Care Access Research process while learning the skills necessary to be a Clinical Research Coordinator.

New!

Tampa, FL6 days ago

$65,000–$95,000 Per Year

With programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. The Clinical Research Coordinator's primary responsibilities are to utilize Good Clinical Practices (GCP)s in the process of screening, enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance.

miami, FL30+ days ago

As a key member of the research team, the Project Manager will be responsible for the day-to-day operations of a large research team including (direct and indirect) supervision of research staff (both junior and senior), post-doctoral candidates, and undergraduate research trainees. Responsibilities include any combination of research participant-related activities such as recruitment, screening, psychiatric assessment, data collection, analysis, and management using electronic data capture systems, interaction with patient's treatment team, imaging acquisition, and preparation of manuscripts.

Tampa, FL30+ days ago

$65,000–$95,000 Per Year

With programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. The Clinical Research Coordinator's primary responsibilities are to utilize Good Clinical Practices (GCP)s in the process of screening, enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance.

Tamarac, FL30+ days ago

$19–$33 Per Hour

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Clinical Research Manager Jobs in Florida

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Clinical Manager of Research Cardiovascular Associates of America

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Director of Clinical Research Site Operations ForCare Clinical Research

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Clinical Research Coordinator II - UF Emergency Medicine University of Florida

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Clinical Research Coord II-Multiple Sclerosis (MS) Division University of Florida

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Clinical Research Analyst II University of Florida

Clinical Research Coord - Day - Full Time - Corp Orlando Health

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Medical Assistant - Clinical Research (Bilingual English/Spanish) - Miami, FL Syneos Health Inc

Clinical Research Support Specialist University of Miami

Clinical Research Coord - Day - Full Time - Corp Orlando Health Ventures l LLC

Senior Clinical Research Associate - Oncology - FSP Parexel

Clinical Research Coordinator Floater - 2nd & 3rd Shift Teva Pharmaceutical Industries Ltd

Sr. Manager, Research Administration (Pre-Award) University of Miami

Clinical Research Associate II/ Bilingual Oncology/ Southeast US Thermo Fisher Scientific Inc

Clinical Research Associate II/ Neurology/ Eastern region of the US! Thermo Fisher Scientific Inc

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RN Clinical Research Night Shift AdventHealth

CLINICAL RESEARCH COORDINATOR I H. Lee Moffitt Cancer Center & Research Institute Inc

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Clinical Research Associate, Sponsor Dedicated IQVIA Holdings Inc

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