Newlinical Research Coordinator (CRC) – Rheumatology Trials Wellnet Research Solutionslinical Research Coordinator (CRC) – Rheumatology TrialsPlantation, FL$52,000–$72,800 / yearFull timePart timeIn this position, you will be responsible for coordinating patient visits, supporting recruitment and follow-ups, maintaining accurate study documentation, and ensuring compliance with study protocols and regulatory requirements. This role is best suited for candidates who have previously worked in clinical trial settings and understand study workflows, patient coordination, and regulatory documentation.
NewPostdoctoral Research Fellow – Wildlife Health and Conservation *St Kitts* Ross University School of Veterinary MedicinePostdoctoral Research Fellow – Wildlife Health and Conservation *St Kitts*Miami, FLRoss University School of Veterinary Medicine (RUSVM) is the number one provider of Doctors of Veterinary Medicine (DVMs) to the U.S.* and offers a DVM program that is accredited by the American Veterinary Medical Association Council on Education. Ross University School of Veterinary Medicine (RUSVM) is inviting applications for one Postdoctoral Research Fellowships in Wildlife Health and Conservation, with a focus on sea turtles, shorebirds, and seabirds.
NewVeterinary Emergency and Critical Care Faculty (St Kitts) Ross University School of Veterinary MedicineVeterinary Emergency and Critical Care Faculty (St Kitts)Miami, FLThis position involves teaching didactic lectures and practical/laboratory sessions in Emergency and Critical Care to Doctor of Veterinary Medicine (DVM) students, as well as providing clinical consultation services in the First Opinion Small Animal Clinic. Ross University School of Veterinary Medicine (RUSVM), a Covista institution, prepares students to become veterinary leaders by drawing connections among animals, people and the planet, as a member of the One Health Initiative.
Senior Clinical Research Associate - Oncology - Florida - FSP Parexel International CorpSenior Clinical Research Associate - Oncology - Florida - FSPFLThe role involves collaboration with cross-functional clinical study teams and investigator site personnel to ensure study deliverables are met efficiently and effectively. Perform review of study metrics, assess CRO Clinical Research Associate (CRA) and Investigator Site performance and identify sites for oversight monitoring visits.
Senior Clinical Research Associate ICON PlcSenior Clinical Research AssociateMiami, FLFlexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
Clinical Research Associate ICON PlcClinical Research AssociateMiami, FLICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a CRA II at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
Clinical Research Associate IV TechDigital CorporationClinical Research Associate IVQuail Heights, FLRemoteIn this role, you will have the opportunity to: • Support development of study essential document templates (e.g., study guides, study tools/worksheets) and ensure Trial Master File (TMF), Sponsor Site Files (SSF), and Investigator Site Files (ISF) are maintained and kept up to date; assist in audit readiness and preparation. The essential requirements of the job include: • Bachelor's degree or equivalent in the life sciences, with 4+ years' work experience in vitro diagnostics (IVD), Medical Device, or Pharmaceutical research; 2+ years' experience with Master's degree, or 1+ years with Doctoral degree.
Sr. Clinical Research Coordinator - Oncology - Onsite (Full Time, Days) Nicklaus Children's HospitalSr. Clinical Research Coordinator - Oncology - Onsite (Full Time, Days)Miami, FLBeyond 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.
Sr. Clinical Research Coordinator - Neurology - Onsite (Full Time, Days) Nicklaus Children's HospitalSr. Clinical Research Coordinator - Neurology - Onsite (Full Time, Days)Miami, FLBeyond 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.
Clinical Research Associate II ICON PlcClinical Research Associate IIMiami, FLAs a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
Clinical Research Scientist, Pediatric Early Phase Clinical Trials Nicklaus Children's HospitalClinical Research Scientist, Pediatric Early Phase Clinical TrialsMiami, FLThe Clinical Research Scientist plays a critical role in protocol development, translational integration, data interpretation, regulatory documentation, and dissemination of research findings, strengthening the scientific rigor and operational success of early‑phase pediatric oncology trials. The Clinical Research Scientist supports the scientific development, implementation, and analysis of early‑phase (Phase I/first‑in‑child) oncology clinical trials within the Clinical Trials Unit at Nicklaus Children's Health System (NCHS).
NewClinical Research Associate 3 University of MiamiClinical Research Associate 3Miami, FLDepartmnet specific functions: Oversees all new referrals to and ongoing clinical practice for the specialty UM Tics, OCD and Related Problems Program and the UM Tourette Association of America (TAA) Center of Excellence Program. 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.
Sr. Clinical Research Coordinator Actalent IncSr. Clinical Research CoordinatorMiami, FL$32–$43 / hourClinical Research Coordinator (SCRC) ensures that clinical studies are conducted in accordance with the protocol, applicable regulations, Good Clinical Practice (GCP), and Institutional Review Board (IRB) requirements. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
Clinical Research Assistant Cardiovascular Associates of AmericaClinical Research AssistantMiami, FLFull timeThis position assists Clinical Research Coordinators (CRCs), investigators, and study teams with participant scheduling, specimen processing, investigational product accountability support, supply management, and study-related documentation. The Clinical Research Assistant plays a critical role in ensuring efficient study conduct while allowing coordinators to focus on protocol management, participant care, and study execution.
NewClinical Research Associate II - US East Region (Northeast & Southeast) - Multiple Therapeutic Areas Available Thermo Fisher ScientificClinical Research Associate II - US East Region (Northeast & Southeast) - Multiple Therapeutic Areas AvailableMiami Beach, FloridaAt least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy. Acting as a site processes specialist, you will ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, well-being, and data reliability.
Oncology Regulatory Research Coordinator II - FT - Days - MCI Clinical Research South Broward Hospital DistrictOncology Regulatory Research Coordinator II - FT - Days - MCI Clinical ResearchPembroke Pines, FLAdditional Job Information: Complexity of Work: Requires critical thinking skills, effective communication skills, decisive judgment and the ability to work with minimal supervision. Responsibilities: Assists in training/mentoring of CRC I and other team members as requiredProcesses and ships research specimens per protocol guidelines.
Clinical Research Coordinator, Oncology Research, FT, 8A-4:30P Baptist Health South Florida IncClinical Research Coordinator, Oncology Research, FT, 8A-4:30PBoca Raton, FLOur approach is rooted in a "grow our own" philosophy, designed to help our team members build meaningful, long-term careers with us, supported by benefits that make a real difference, including: Career growth and development opportunities, with clear pathways and ongoing support. Baptist Health is the region''s largest not-for-profit healthcare organization, with 12 hospitals, over 29,000 employees, 4,500 physicians and 200 outpatient centers, urgent care facilities and physician practices across Miami-Dade, Monroe, Broward and Palm Beach counties.
NewClinical Research Coordinator 2, MCVI Research, FT, 8A-4:30P Baptist Health South Florida IncClinical Research Coordinator 2, MCVI Research, FT, 8A-4:30PCoral Gables, FLOur approach is rooted in a "grow our own" philosophy, designed to help our team members build meaningful, long-term careers with us, supported by benefits that make a real difference, including: Career growth and development opportunities, with clear pathways and ongoing support. Baptist Health is the region''s largest not-for-profit healthcare organization, with 12 hospitals, over 29,000 employees, 4,500 physicians and 200 outpatient centers, urgent care facilities and physician practices across Miami-Dade, Monroe, Broward and Palm Beach counties.
Clinical Research Associate II/ Neurology/ Eastern region of the US! Thermo Fisher Scientific IncClinical Research Associate II/ Neurology/ Eastern region of the US!Miami Beach, FLWhat 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.
Associate Director, Pediatric Clinical Research - Cancer Center Nicklaus Children's HospitalAssociate Director, Pediatric Clinical Research - Cancer CenterMiami, FLThe Associate Director of Pediatric Clinical Research - Cancer Center, serves as the senior operational and execution leader for all pediatric cancer clinical research activities within the Cancer Center, including early phase (Phase I/first in child), investigator initiated, cooperative group, and sponsor driven trials supported by the CORKK and Cancer Center grant portfolio. Provides oversight and scientific direction in protocol development, translational integration, data interpretation, regulatory documentation, and dissemination of research findings, while retaining responsibility for operations, performance, governance, and program execution.
Clinical Research Associate, Sponsor Dedicated IQVIA Holdings IncClinical Research Associate, Sponsor DedicatedFort Lauderdale, FLEnsure 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.
Senior Clinical Research Coordinator – Hematology/Oncology Inspire Path Networks, LLCSenior Clinical Research Coordinator – Hematology/OncologyMiami, FloridaThis is a fully onsite position located on the main corporate campus and is ideal for an experienced research professional who is comfortable managing high-enrollment studies and complex clinical trial activities. Clinical Research Coordinator will independently manage the day-to-day operations of assigned studies while ensuring compliance with study protocols, GCP guidelines, IRB requirements, and FDA regulations.
Clinical Research Coordinator 3 University of MiamiClinical Research Coordinator 3Miami, FLThis 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.
Clinical Research Coordinator 3 (A) University of MiamiClinical Research Coordinator 3 (A)Miami, FLThis 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.
Clinical Research Associate IREClinical Research AssociateMiami, FloridaWilling and able to travel up to 50% for on-site monitoring visits across southeast region; preference given to candidates residing in Miami, FL near major HUB airports to support efficient regional travel. ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
Clinical Research Associate II IREClinical Research Associate IIFort Lauderdale, FloridaWilling and able to travel up to 50% for on-site monitoring visits across southeast region; preference given to candidates residing in West Palm Beach, FL near major HUB airports to support efficient regional travel. ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
Clinical Research Associate II (Part-time Contract) Premier Research International LLCClinical Research Associate II (Part-time Contract)FLWhat you'll be doing: Perform monitoring activities (both on site and remote) including Site Qualification Visits, Site Initiation Visits, Interim Monitoring Visits, Site Management Contacts, Close Out Visits for Phase I-IV clinical trials. Serve as the primary point of contact for investigative sites, manage query resolution, support Trial Master File activities, participate in Investigators' Meetings, and complete other project tasks in accordance with study timelines and budget.
Clinical Research Coord II Integrated Resources, IncClinical Research Coord IIMiami, FLLogs/completes information on sponsor systems and ensures all information provided is accurate (i.e., case report forms, EDC, etc.) and ensures it is completed within timeframe. "Performs all defined study activities (i.e., informed consent, screening, and protocol procedures which include but not limited to vital signs, pregnancy tests, height, weight, ECG's, etc.).
Clinical and Health - Clinical Research Coord II MindlanceClinical and Health - Clinical Research Coord IIMiami, FLLogs/completes information on sponsor systems and ensures all information provided is accurate (i.e., case report forms, EDC, etc.) and ensures it is completed within timeframe. " Performs all defined study activities (i.e., informed consent, screening, and protocol procedures which include but not limited to vital signs, pregnancy tests, height, weight, ECG's, etc.).
Clinical Research Associate I (East Coast: NY, FL, NJ, PA, OH, DC, MD) Premier Research International LLCClinical Research Associate I (East Coast: NY, FL, NJ, PA, OH, DC, MD)FLYou will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. Premier Research is looking for a Clinical Research Associate I (East Coast: NY, FL, NJ, PA, OH, DC, MD) to join our Global Clinical Monitoring and Site Management team.
Clinical Research Associate III - 991369 NSUClinical Research Associate III - 991369Fort Lauderdale, FloridaActive Listening - Proficient skills in giving full attention to what other people are saying, taking time to understand the points being made, asking questions as appropriate, and not interrupting at inappropriate times. Critical Thinking - Proficient skills in using logic and reasoning to identify the strengths and weaknesses of alternative solutions, conclusions, or approaches to problems.
Clinical Research Associate III - 991388 NSUClinical Research Associate III - 991388Fort Lauderdale, FloridaActive Listening - Proficient skills in giving full attention to what other people are saying, taking time to understand the points being made, asking questions as appropriate, and not interrupting at inappropriate times. Critical Thinking - Proficient skills in using logic and reasoning to identify the strengths and weaknesses of alternative solutions, conclusions, or approaches to problems.
General Dermatologist in Clinical Research | Skin And Cancer Associates | Aventura, FL West DermatologyGeneral Dermatologist in Clinical Research | Skin And Cancer Associates | Aventura, FLAventura, FloridaWe’re looking for a General Dermatologist with interest in doing Clinical Research to join our friendly, highly trained team dedicated to clinical excellence and an outstanding patient experience. At Platinum Dermatology Partners, we're not just advancing dermatology; we're shaping its future by fostering an environment where physician leadership drives clinical decisions, and our expertise optimizes practice operations and growth.
Clinical Research Associate III - 991388 Nova Southeastern UniversityClinical Research Associate III - 991388FLSkills: Active Listening - Proficient skills in giving full attention to what other people are saying, taking time to understand the points being made, asking questions as appropriate, and not interrupting at inappropriate times. Job Requirements: Required Knowledge, Skills, & Abilities: Knowledge: English Language - General knowledge of the structure and content of the English language including the meaning and spelling of words, rules of composition, and grammar.
Clinical Research Associate III - 991369 Nova Southeastern UniversityClinical Research Associate III - 991369FLSkills: Active Listening - Proficient skills in giving full attention to what other people are saying, taking time to understand the points being made, asking questions as appropriate, and not interrupting at inappropriate times. Job Requirements: Required Knowledge, Skills, & Abilities: Knowledge: English Language - General knowledge of the structure and content of the English language, including the meaning and spelling of words, rules of composition, and grammar.
NewRegional Travel, Clinical Research Coordinator Care AccessRegional Travel, Clinical Research CoordinatorTamarac, FLRemote$75,000–$105,000 / yearWith 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.
Supervisor Clinical Research Coordinator, Miami Cancer Institute, FT, 8:00A - 4:30P Baptist Health South Florida IncSupervisor Clinical Research Coordinator, Miami Cancer Institute, FT, 8:00A - 4:30PMiami, FL$83,400.24–$108,420.31 / yearOur approach is rooted in a "grow our own" philosophy, designed to help our team members build meaningful, long-term careers with us, supported by benefits that make a real difference, including: Career growth and development opportunities, with clear pathways and ongoing support. Baptist Health is the region''s largest not-for-profit healthcare organization, with 12 hospitals, over 29,000 employees, 4,500 physicians and 200 outpatient centers, urgent care facilities and physician practices across Miami-Dade, Monroe, Broward and Palm Beach counties.
Clinical Research Support Specialist University of MiamiClinical Research Support SpecialistMiami, FLVisits 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.
Clinical Research Data Assistant Cardiovascular Associates of AmericaClinical Research Data AssistantMiami, FLFull timeThe Clinical Research Data Assistant works closely with Clinical Research Coordinators, investigators, sponsors, and the regulatory team to ensure accurate, timely, and compliant study documentation and reporting. The Clinical Research Data Assistant provides administrative, data management, and study support services for clinical research studies.
PRN - Clinical Research RN I Research Centers of AmericaPRN - Clinical Research RN IHollywood, FLPart timeRecently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials. Provides general nursing care to study participants as necessary; including, but not limited to monitoring of vitals, blood sugar, vital signs, lab tests, etc.
Clinical Research Nurse (Full Time, Days) Nicklaus Children's HospitalClinical Research Nurse (Full Time, Days)Miami, FLBSN - 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.
Quality Assurance Coordinator (Clinical Research) Research Centers of AmericaQuality Assurance Coordinator (Clinical Research)Hollywood, FLPart timeGCP, 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.
Medical Assistant (Clinical Research) Research Centers of AmericaMedical Assistant (Clinical Research)Hollywood, FLPart timep>With moderate oversight, the Research Assistant I provides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies. Recently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials.
NewClinical Research Coordinator 2 - CRANE Lab University of MiamiClinical Research Coordinator 2 - CRANE LabMiami, FLUnlike traditional therapeutic clinical trials that are primarily focused on investigational drugs, devices, and sponsor-driven regulatory activities, many CRANE Lab studies involve intensive participant engagement, behavioral assessment, lifestyle intervention delivery, patient-reported outcomes, and longitudinal participant support. 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.
NewRegional Travel, Clinical Research Coordinator Care Access Research LLCRegional Travel, Clinical Research CoordinatorTamarac, FLRemote$75,000–$105,000 / yearWith 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.
Director, Clinical Research University of MiamiDirector, Clinical ResearchMiami, FLCollaborates cross-functionally with Clinical Operations, Regulatory Affairs, and Project Management areas and appropriately utilizes external vendors (e.g., CRO, consultants, etc.) to ensure study objectives/timelines are met, and activities are conducted in accordance with applicable regulations. The Director, Clinical Research provides oversight, leadership, strategic insight, direction and implementation throughout the lifecycle of a clinical trial or research study.
Clinical Research Participant Specialist University of MiamiClinical Research Participant SpecialistMiami, FLVisits 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. UHealth-University of Miami Health System, South Floridas 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.
Patient Recruitment Manager (Clinical Research) Research Centers of AmericaPatient Recruitment Manager (Clinical Research)Hollywood, FLPart timeWe 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.
Clinical Research Coordinator II - FT - Days - OHR South Broward Hospital DistrictClinical Research Coordinator II - FT - Days - OHRHollywood, FLAdditional Job Information: Complexity of Work: Requires critical thinking skills, effective communication skills, decisive judgment and the ability to work with minimal supervision. Coordinates the preparation and delivery of departmental communications, presentations and marketing/educational materials.