692 Results for

Clinical Research Associate Jobs in Florida

Jobs

Gainesville, FL7 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. As a majority owner of Galen College of Nursing, which joins Research College of Nursing and Mercy School of Nursing as educational facilities within the HCA Healthcare family, we make it easier and more affordable to gain certifications and job skills.

Gainesville, FL7 days ago

FL26 days ago

The 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.

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.

Quail Heights, FL30+ days ago

Remote

In 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.

Miami, FL30+ days ago

Flexible 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.

Tampa, FL10 days ago

ICON 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.

Miami, Florida10 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.

Jacksonville, FL8 days ago

$24.55–$35.65 Per Hour

Minimum Education and/or Experience Required: (Education Requirements and Experience): HS Diploma with at least 3 years of experience OR Associate's degree/college Diploma/Certificate Program with at least 1 year of experience, Associate's in Clinical Research from an accredited academic institution without experience OR Bachelor's degree. Position Overview: (Major Functions and Non-Essential Functions): Coordinates non-therapeutic (i.e. minimal risk, survey, chart review) clinical research protocols with direction from the principal investigator and/or supervisor in compliance with regulatory laws and institutional guidelines.

Miami, FL22 days ago

As 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.

Miami, Florida19 days ago

Miami Beach, Florida30+ days ago

We offer the latest in advanced medicine, technology, and comfort in 12 facilities across Miami-Dade (including our 674-bed main campus facility) and Monroe Counties, with 38 medical services, including cancer care, 24/7 emergency care, orthopedics, cardiovascular care, and more. Createsan educational outreach platform in partnership with local healthcare providers and community organizations to raise awareness about current research initiatives and clinical trial opportunities.

Port Saint Lucie, 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 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

FL27 days ago

You 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.

New!

Naples, FL6 days ago

We value employee experience, well-being and mental health and we acknowledge that a healthy work life balance is a critical factor for employee satisfaction and in turn nurtures an environment from which a high-quality client service can be achieved. Performs on-site or remote Pre-Study, Initiation, Interim, and Close-Out monitoring visit activities to ensure that facilities and staff at the investigational site continue to be adequate for the conduct of the study.

Princeton, Florida19 days ago

This person has the responsibility to guide and supervise clinical research activities performed by external vendors (CROs), consultant monitors (when applicable) and clinical study assistants working on assigned projects. The Associate Director/ Director, Clinical Research is person is responsible for leading clinical research activities for a specific program or programs as well as managing all activities associated with performing one or more clinical studies.

Fort Lauderdale-Davie, FL25 days ago

Skills: 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.

Gainesville, FL30+ days ago

Three of the Colleges academic programs occupytop-20spots in the U.S. News rankings: Counselor Education (1st), Special Education (4th), and Elementary Education (14th).Cutting-edgeinterdisciplinary research and public scholarship-often conducted in partnership with other UF colleges, school districts and communities across the state and nation-are yielding powerful learning systems and models that are helping to transform education in today's changing world, starting with our youngest learners. Successful candidates willdemonstratethe ability to teach applied researchmethodologycoursesinqualitative research methodsto bothREM majors and non-majors, show a commitment to graduate education, and serve on program, school, college, anduniversity committees.

Tampa, FL30+ days ago

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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, FL17 days ago

$32–$43 Per Hour

Clinical 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.

Miami, FL30+ days ago

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FL30+ days ago

$115,500–$204,600 Per Year

Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). CRLs partner closely with internal Lilly teams (including Clinical Development and Medical Affairs) to ensure that insights from the field shape development strategies and that development strategies are delivered with operational excellence and scientific clarity.

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.

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.

Miami, FL30+ days ago

Baptist Health is the region's largest not-for-profit healthcare organization, with 12 hospitals, over 28,000 employees, 4,500 physicians and 200 outpatient centers, urgent care facilities and physician practices across Miami-Dade, Monroe, Broward and Palm Beach counties. For 25 years, we've been named one of Fortune's 100 Best Companies to Work For, and in the 2024-2025 U.S. News & World Report Best Hospital Rankings, Baptist Health was the most awarded healthcare system in South Florida, earning 45 high-performing honors.

Tampa, FL30+ days ago

Credentials and Qualifications: • Bachelor's degree with 2 years clinical trials coordination experience • In lieu of a bachelor's degree, an associate's degree with 4 years clinical trials coordination experience may be considered • CCRP/CCRC certification preferred. 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.

Ocala, Florida30+ days ago

Special knowledge of GCP and ICH guidelines preferred Knowledge of medical terminology, nursing assessment, clinical medicine, diagnostic tests, radiology, pathology, pharmacology, hematology, oncology as it relates to clinical trials Working Conditions: Environment (Office, warehouse, etc.). Oncology Supervisory experience preferred, experience in clinical research preferred If required in state of practice, current licensure as a registered (RN) Current BCLS or ACLS certification for nurses SoCRA or ARCP certification preferred Specialized Knowledge/Skills.

Miami, Florida26 days ago

This 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.

New!

Tampa, 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 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.

New!

Palm Beach Gardens, FL2 days ago

Full-time

Position Overview: As a Clinical Research Coordinator, you will play a key role in managing and overseeing all aspects of clinical trials and site operations. About CVAUSA: Cardiovascular Associates of America (CVAUSA) is a rapidly growing leader in cardiovascular care, committed to advancing medical research and improving patient outcomes.

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.

Orlando, FL30+ days ago

$65,622.66–$122,055.21 Per Year

The expertise and experiences you'll need to succeed: QUALIFICATION REQUIREMENTS: • Associates of Nursing (Required) • Bachelors of Nursing (Required) • Advanced Cardiac Life Support Cert (ACLS - RQI Resuscitation Quality Improvement) • Basic Life Support - CPR Cert (BLS - RQI Resuscitation Quality Improvement) • Certified Clinical Research Coordinator (CCRC - EV Accredited Issuing Body) • Registered Nurse (RN - EV Accredited Issuing Body) • Society of Clinical Research Associates (SOCRA - EV Accredited Issuing Body). Delivers effective and compliant clinical research study coordination, including planning, organizing, and managing all activities related to clinical research protocols.

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.

Tampa, FL30+ 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.

Orlando, FL8 days ago

$49,307.53–$91,705.34 Per Year

Detail oriented and has teamwork skills; motivated, organized, ability to perform multiple tasks in a timely manner, and work efficiently under pressure Simultaneously executes and coordinate multiple clinical trials and function independently; perform diverse clinical and clerical duties Other duties as assigned. Additional Information: An equivalent combination of education ad relevant work experience may be considered in lieu of the stated degree requirement: - Bachelors degree and 2+ years of experience OR - Associates degree and 4+ years of experience OR - Technical/Vocational School and 6+ years of clinical research experience.

Winter Park, FL7 days ago

$49,307.53–$91,705.34 Per Year

Panama City, FL30+ days ago

The CRC will be responsible for the day-to-day coordination and execution of clinical trials, ensuring compliance with protocols, regulatory requirements, and Good Clinical Practice (GCP). Accurately document study data in source documents and electronic data capture (EDC) systems .

New!

Gainesville, FL4 days ago

$46,000–$48,000 Per Year

Researches regulatory compliance participation in activities to initiate and maintain a current regulatory file; prepares and submits documents related to research protocols to both internal (UF-IRB, UF-CTC office, UF-OCR, etc.) and external (FDA, WIRB, etc.) organizations as required; completes end-of-study procedures; schedules and participates in sponsored research monitoring visits and QA audits; ensures the integrity and quality of the research protocol is maintained and the trial is conducted in accordance with GCP guidelines; attends UF-IRB 01 full board meetings as necessary. Job Description:Selects and recruits study participants to enroll in various studies and protocols; participates in the informed consent process of study subjects; supports the safety of clinical research patients/research participants; coordinates protocol-related research procedures, study visits, and follow-up care; screens, completes case report forms (paper & electronic data capture), and addresses queries.

New!

Orlando, Florida2 days ago

In addition to being accredited by the Commission on Cancer, a program of the American College of Surgeons, Orlando Health Cancer Institute has earned accreditations and certifications in several areas — including medical oncology and hematology/oncology, radiation oncology, cellular therapy, rectal cancer, and breast care — from the respective accrediting organizations, and recently was named in the 2023 Becker's Hospital Review “60 Hospitals and Health Systems with Great Oncology Programs” list. Orlando Health Cancer Institute is part of the Orlando Health system of care, which includes 24 award-winning hospitals and ERs, 9 specialty institutes, 14 urgent care centers, 100+ primary care practices and more than 60 outpatient facilities that span Florida’s east to west coasts and beyond.

Orlando, FL30+ days ago

$65,582.40–$108,646.85 Per Year

Knowledge, Skills, and Abilities: Ability to perform clinical tasks including assisting physician, ARNP and CRN with minor procedures and other study requirements within scope of practice. Ability to work independently in a fast-paced clinical or research environment, handling multiple tasks simultaneously, effectively, and in an organized and timely manner [Required].

New!

Gainesville, FL2 days ago

$46,000–$53,000 Per Year

As part of an interdisciplinary health team, the incumbent will collaborate with other CRCs, physicians, nurses, and other key personnel in the department and clinic to ensure compliance with protocol requirements and satisfactory care for enrolled patients. Job duties include, but are not limited to: Coordination of Protocol Subjects & Data Collection:Perform subject screening and consent for clinical protocols under direction of the Principal Investigator (PI).

Orlando, FL30+ days ago

Qualifications Education/Training Must meet one of the following: • Bachelor's degree in health-related field (i.e., Healthcare Administration, 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). Education/Training Must meet one of the following: • Bachelor's degree in health-related field (i.e., Healthcare Administration, 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).

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.

Jacksonville, FL9 days ago

$90,000–$130,000 Per Year

This includes day-to-day operations, protocol and specimen guidance, tracking of all clinical research studies, and weekly coordinator meetings for a department with over 55 clinical studies, and EM Research Laboratory, and 7 day per week and evening coordinator coverage. Provides regular updates of clinical research studies progression to PIs, leadership, and study sponsors; proactively identifies and resolves issues during study implementation and dissemination; and manages escalation of study-related issues.

Sarasota, FL18 days ago

May be responsible for providing coverage in clinics when research staff are out of the office; for precepting new research staff in clinics; for assisting with research projects assigned by the Senior Clinical Research Coordinator III. Candidates must have a valid RN license, in state of employment, a minimum of one-year oncology or clinical research experience; or a minimum of five years of combined clinical oncology and clinical research experience.

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Clinical Research Associate Jobs in Florida

Clinical Nurse Coord Intermediate Care Unit HCA Florida North Florida Hospital

RN Med Surg Clinical Decision Unit HCA Florida North Florida Hospital

RN Med Surg Clinical Observation Unit HCA Florida North Florida Hospital

Senior Clinical Research Associate - Oncology - Florida - FSP Parexel International Corp

Senior Clinical Research Associate - Oncology - FSP Parexel

Clinical Research Associate IV TechDigital Corporation

Senior Clinical Research Associate ICON Plc

Clinical Research Associate ICON Plc

Clinical Research Associate IRE

CLINICAL RESEARCH COORD ASSOCIATE H. Lee Moffitt Cancer Center & Research Institute Inc

Associate Clinical Research Coordinator for Women's Health Mayo Clinic

Clinical Research Associate II ICON Plc

Clinical Research Associate II IRE

Clinical Research Associate for Memory Disorders Mount Sinai Medical Center of Florida

Clinical Research Associate, Sponsor Dedicated IQVIA Holdings Inc

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

Clinical Research Associate I (East Coast: NY, FL, NJ, PA, OH, DC, MD) Premier Research International LLC

Senior Clinical Research Associate (Florida) Ergomed Group Ltd

Associate Director, Clinical Research Bracco

Clinical Research Associate III - 991388 Nova Southeastern University

Clinical Assistant/Associate Professor of Qualitative Research Methodology University of Florida

Sr. Clinical Research Associate, IQVIA IQVIA Holdings Inc

Sr. Clinical Research Coordinator - Neurology - Onsite (Full Time, Days) Nicklaus Children's Hospital

Sr. Clinical Research Coordinator Actalent Inc

Home Based Experienced CRA (Clinical Research Associate) Bonus/Equity Medpace Holdings Inc

Associate Director - Clinical Research Lead-Oncology (Florida, Puerto Rico) Eli Lilly and Co

Clinical Research Coordinator 3 University of Miami

Clinical Research Coordinator 3 (A) University of Miami

Research Associate 3, Oncology Clinical Trials, FT, 8:00A - 4:30P-154294 Baptist Health South Florida Inc

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

Associate Director Clinical Research Florida Cancer Affiliates

Senior Clinical Research Coordinator – Hematology/Oncology Inspire Path Networks, LLC

Clinical Research Coordinator III Care Access

RN or LPN Clinical Research Coordinator Cardiovascular Associates of America

Sr. Clinical Research Coord - ONSITE (Full Time, Days) Nicklaus Children's Hospital

Supv, Clinical Research RN AdventHealth

Clinical Research Coordinator III Care Access Research LLC

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

Clinical Research Coordinator II Orlando Onsite AdventHealth

Clinical Research Coordinator II AdventHealth

Clinical Research Coordinator - Part Time GULF COAST HEART AND VASCULAR LLC

Clinical Research Coordinator I University of Florida

Clinical Research Lead - Orlando Health Cancer Institute Orlando Health

Clinical Research Coordinator I RN AdventHealth

Clinical Research Coord I-Transplant Center University of Florida

Clinical Research Coord - Corp Orlando Health Ventures

Clinical Research Assistant University of South Florida

Assistant Director, Clinical Research - -Emergency Medicine Research University of Florida

Clinical Research Coordinator III Drug Development Unit Florida Cancer Specialists and Research Institute

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