clinical research coordinator (in-person)

prn clinical research infusion registered nurse (rn)

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clinical research coordinator (in-person) Jobs in Tampa

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vp cancer clinical research

Cancer Center of South Florida

<div>Description:

POSITION SUMMARY: 
The Vice President of Clinical Research serves in a dyad leadership model with the Associate Director of Clinical Investigations to lead and advance all cancer-related clinical research at Tampa General Hospital Cancer Institute. This role provides strategic and operational leadership to grow a high-quality, compliant, and innovative clinical research enterprise. The VP is responsible for expanding clinical research programs, strengthening infrastructure, and building a multi-site research network that increases access to clinical trials across current and future sites of care. This leader partners with academic institutions, industry sponsors, and internal stakeholders to advance research initiatives and position the organization for future designation by the National Cancer Institute. The role also oversees clinical research operations, including the Clinical Trials Office (CTO) and PRMS program, and leads the development of a high-performing research workforce while ensuring compliance with all applicable regulatory requirements.
Requirements: 
CORE ESSENTIAL RESPONSIBILITIES:<ul><li>
Develops and executes the clinical research strategy to advance the cancer research enterprise and achieve NCI-designation, including expansion of an academic-community clinical trials network and across the populations and communities served.</li><li>
Designs, implements, and sustains a compliant and scalable clinical research infrastructure, including regulatory frameworks, operational processes, and enterprise-wide systems that support the Clinical Cancer Trials Office (CCTO) and research activities.</li><li>
Ensures regulatory compliance and research integrity by establishing and maintaining programs that meet all applicable federal, state, and institutional requirements (including FDA, IRB, and Good Clinical Practice), including oversight of sponsor-investigator trials.</li><li>
Provides executive leadership and oversight of clinical research operations, including the Clinical Trials Office (CTO) and PRMS program, ensuring efficient, high-quality study execution, appropriate resource allocation, and financial performance across all sites.</li><li>
Establishes and expands strategic partnerships and the clinical research network, including collaboration with academic institutions, industry sponsors, and community organizations to increase access, participation, and innovation in clinical trials.</li><li>
Builds, leads, and develops a high-performing clinical research workforce, including organizational design, staffing models, performance management, and training to ensure operational effectiveness, compliance, and succession planning.</li></ul>
 REQUIRED EDUCATION &amp; EXPERIENCE<ul><li>
Master&rsquo;s Degree or PhD in healthcare related field required.</li><li>
A minimum of ten (10) years&rsquo; experience in oncology.</li><li>
A minimum of ten (10) years&rsquo; experience in clinical research leadership.</li><li>
Experience in oncology and clinical research leadership with an NCI-designated comprehensive cancer center is highly desirable.</li><li>
Experience in clinical research leadership in a matrix environment that requires interaction and close coordination with several stakeholders (ie. colleges, institutes and departments).</li></ul> 
REQUIRED KNOWLEDGE, SKILLS OR ABILITIES<ul><li>
Clinical research regulations and standards (FDA, IRB, Good Clinical Practice).</li><li>
Clinical trials operations across the full study lifecycle (start-up through closeout).</li><li>
Research infrastructure, including regulatory, data management, budgeting, and quality systems.</li><li>
Sponsor-investigator requirements (e.g., IND/IDE processes).</li><li>
Healthcare systems and academic medical center environments.</li><li>
Financial management principles within clinical research.</li><li>
Strategic planning and program development in a healthcare or research setting.</li><li>
Compliance, risk management, and quality improvement practices.</li><li>
Partnership development across academic, industry, and community organizations.</li></ul></div>

VP, Cancer Clinical Research

Moffitt Cancer Center

<div>Premi Lab is leading cutting-edge research into the complex interplay between metabolic enzymes, pigmentary systems, and redox pathways in skin carcinogenesis. Our current projects focus on investigating novel plant-based compounds to counteract the harmful effects of ultraviolet radiation, including direct and indirect DNA damage, redox stress, and enhanced photoprotection.
<div>We are seeking a highly motivated and skilled individual to join our team in this exciting RAI position. The ideal candidate will have some hands-on experience with core cellular and molecular biology techniques, including: 
<ul><li>Mammalian cell culture (experience with both primary cells and cell lines is preferred)</li><li>DNA/RNA analysis, including DNA processing, DNA damage, and repair analysis.</li><li>Immunodetection methods, such as Western blotting, ELISA, and immunohistochemistry (IHC).</li><li>Fluorescence and brightfield microscopy, along with imaging and image analysis using ImageJ or other relevant platforms.</li><li>Data analysis using GraphPad Prism or similar software.</li></ul></div> 
If you are passionate about advancing our understanding of skin cancer biology and developing innovative therapeutic strategies, we encourage you to apply. Join us in making a meaningful impact on skin health and cancer prevention! 
<div> 
Ideal Candidate: 
<ul><li>Ability to plan, organize and coordinate work assignments.</li><li>Ability to establish and maintain effective working relationships with others and communicate clearly, verbally and in writing.</li></ul></div>
<div>Responsibilities: 
<ul><li>Maintains laboratory equipment in a clean and working order, including coordinating instrument standardization documented by written report.</li><li>Reorders stock laboratory supplies when depleted under appropriate supervision.</li><li>Contributes to the preparation of manuscripts, grants, administrative and research compliance documents as directed by supervisor.</li><li>Technically responsible for the collection, organization and permanent documentation of data in physical and electronic formats as directed by immediate supervisor.</li><li>Responsible for data analysis using standardized procedures and protocols and under minimal supervision.</li></ul></div>
Credentials and Qualifications:
Bachelor&rsquo;s degree in science in molecular biology or in a related field is required and prior research training experience. 
 
Location: H. Lee Moffitt Cancer Center &amp; Research Institute &middot; Tumor Biology 
Schedule: Full Time, Day Shift, varies</div>

RESEARCH ASSOCIATE I

<div>Position Highlights:
The Change Communications Manager leads communication strategies that guide the organization through significant operational, clinical and technological advancements and change across key stakeholder populations. The position partners directly with executive leadership, serving as a strategic advisor and expert storyteller. In addition, the manager functions as an organizational patient communication expert, ensuring messaging is clear, accessible, compassionate, and aligned with Moffitt&rsquo;s commitment to exceptional patient care. 

Credential and Qualifications:
<ul><li>Bachelor&rsquo;s Degree in Journalism, Public Relations, or Communications.</li></ul> 

<ul><li>Minimum five (5) years' experience working with organizational leadership groups to develop executive and organizational communications and executing internal, corporate or external communications or related strategies for engaging large populations of people in a health care, community, public relations or related environment.</li></ul> 

Responsibilities:
Lead Communication Planning for Strategic Efforts
<ul><li>Develop and execute communication strategies for major clinical, operational, and organizational initiatives.</li>
<li>Build communication plans that support awareness, readiness behavior change, and sustained adoption.</li>
<li>Collaborate with MMG leadership, clinical operations, hospital operations, and project teams to ensure messaging reflects real-world impacts and organizational priorities.</li>
<li>Maintain communication calendars, message maps, and stakeholder matrices.</li>
<li>Gather feedback, track communication effectiveness, and adjust plans accordingly.</li>
<li>Support real-time communication needs during critical operational changes and major milestones.</li></ul> 

Develop Leadership Communications
<ul><li>Draft messages, presentations, updates, and briefings for the Physician-in-Chief and Chief Operating Officer.</li>
<li>Build communication plans that enhance leadership visibility and alignment across MMG and hospital operations.</li>
<li>Advise senior leaders on communication tone, timing, and approach.</li></ul> 

Create Content and Messaging
<ul><li>Create compelling content including emails, FAQs, presentations, intranet articles, talking points, and system-wide announcements.</li>
<li>Translate complex clinical, operational, and technical information into audience-appropriate messaging.</li>
<li>Maintain consistency in tone, brand, and voice across all channels.</li></ul> 

Lead Patient Communications Planning and Coordination
<ul><li>Lead strategy, planning, and development of patient-facing communication for major initiatives.</li>
<li>Develop patient letters, FAQs, signage, website content, social media messaging, and appointment-related materials.</li>
<li>Work with Patient Experience, Clinics, Operations, and Marketing to ensure communications are empathetic and easy to understand.</li></ul> 

Lead Stakeholder Engagement and Coordination
<ul><li>Provide communication guidance and regular updates to project sponsors, clinical leaders, and executives.</li>
<li>Facilitate message-alignment sessions, briefings, and communication-focused meetings.</li>
<li>Coordinate with cross-functional partners to ensure timely and accurate information flow.</li></ul> 
 
Location: H. Lee Moffitt Cancer Center &amp; Research Institute &middot; Strategic Communications 
Schedule: Full Time, Day Shift, M-F; 8-5</div>

Change Communications Manager

<div>Position Highlights:
<ul><li>Medical Assistants are essential members of the clinic team. They contribute to the healthcare of patients by assisting with exams and procedures, organizing and managing patient flow, and taking on other responsibilities based on the needs of the department.</li>
</ul>
The Ideal Candidate
<ul><li>The ideal candidate will have the following:
<ul><li>Prior experience in an outpatient clinic setting as a Medical Assistant.</li>
<li>Prior experience performing phlebotomy.</li>
</ul></li></ul>Responsibilities:
<ul><li>Assists patients with ambulation and/or movement on/off exam table, chairs and/or in and out of wheelchairs utilizing proper body mechanics and safety measures such as, lift equipment.</li>
<li>After proper patient identification, performs initial patient screening, including vital signs, screening questions, allergy information, and medication history as appropriate. Notifies appropriate staff of positive screening or abnormal vital signs. Documents collected data completely and accurately in medical record including staff notifications. Loads images in preparation for provider visit, as needed. Ensures clinic patient flow is smooth and efficient. Keeps patients and clinical team informed of delays. Communicates effectively to patients, providers, nurses, and other team members.</li>
<li>Assists practitioner in patient procedures/treatments/examinations, including room preparation, patient positioning, supplies, and equipment. Departs from clinic those patients that do not require nursing intervention. Maintains and uses principles of aseptic techniques and universal precautions when performing clinical duties and tasks.</li>
<li>Maintains the knowledge and skill necessary to provide care or services based on physical, psychosocial, educational, safety, and related criteria appropriate to the age of the patients served in the assigned service area. Utilizes computerized systems according to departmental needs.</li>
<li>Provides support to the provider during clinic by assisting with phone calls and faxes.</li>
<li>Recognizes emergency situations and implements emergency procedures. Administers first aid and CPR.</li>
</ul>
Credentials and Qualifications (per Medical Assistant level):
<ul><li>Moffitt accepted certifications listed below.</li></ul> 

Medical Assistant Trainee:
<ul><li>High school diploma or GED, required.</li>
<li>BLS, required.</li>
<li>Completion of Medical Assistant Program</li>
<li>CMA Certification required within 6 months from date of hire.</li>
</ul>
 
Location: H. Lee Moffitt Cancer Center &amp; Research Institute &middot; MAS Clinic 
Schedule: Full Time, Day Shift, Monday through Friday, 8a-430p</div>

CERTIFIED MEDICAL ASSISTANT MAC FLOAT

HCA Florida South Tampa Hospital

<div>This position is incentive eligible. 
 
 
<h5 class="jobSectionHeader">Introduction</h5>
Managers thrive with us! HCA Healthcare is one of the nation&rsquo;s leading providers of healthcare services, comprising of over 180 hospitals and about 2,000 sites of care in 21 states and the United Kingdom. We are looking for a VP of Quality and Patient Safety for our HCA Florida South Tampa Hospital team where excellence creates excellence.<h5 class="jobSectionHeader">
Benefits</h5>
HCA Florida South Tampa Hospital, offers a total rewards package that supports the health, life, career and retirement of our colleagues. The available plans and programs include:<ul><li>
Comprehensive medical coverage that covers many common services at no cost or for a low copay. Plans include prescription drug and behavioral health coverage as well as free telemedicine services and free AirMed medical transportation.</li><li>
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.</li><li>
Free counseling services and resources for emotional, physical and financial wellbeing 
</li><li>
401(k) Plan with a 100% match on 3% to 9% of pay (based on years of service) 
</li><li>
Employee Stock Purchase Plan with 10% off HCA Healthcare stock 
</li><li>
Family support through fertility and family building benefits with Progyny and adoption assistance. 
</li><li>
Referral services for child, elder and pet care, home and auto repair, event planning and more 
</li><li>
Consumer discounts through Abenity and Consumer Discounts 
</li><li>
Retirement readiness, rollover assistance services and preferred banking partnerships 
</li><li>
Education assistance (tuition, student loan, certification support, dependent scholarships) 
</li><li>
Colleague recognition program 
</li><li>
Time Away From Work Program (paid time off, paid family leave, long- and short-term disability coverage and leaves of absence) 
</li><li>
Employee Health Assistance Fund that offers free employee-only coverage to full-time and part-time colleagues based on income.</li></ul>
Learn more about Employee Benefits
Note: Eligibility for benefits may vary by location. 
HCA Healthcare has expanded our influence across the healthcare industry by investing $3.5 billion in capital improvements in recent years. Do you want to be an influencer in healthcare? Apply for our VP of Quality and Patient Safety role today!<h5 class="jobSectionHeader">
Job Summary and Qualifications</h5>
We are seeking a Vice President, Quality and Safety. You will be responsible for developing and executing organizational quality and performance improvement. You will also be responsible for leadership and organizational wide direction in ensuring a continuously improving culture of safety. We are an amazing team that works hard to support each other and are seeking a phenomenal addition like you who feels patient care is as meaningful as we do. Take the next step in your career.
Responsibilities:<ul><li>You will facilitate and direct organizational wide risk management program to ensure compliance with statutory mandates, regulatory requirements and accreditation standards of professional organizations, i.e., JCAHO, OSHA, etc.</li><li>You will develop and implement educational programs for employees, medical staff and board members on analysis of risk assessment, historical and concurrent occurrence and claims data and national trends.</li><li>You will ensure responsibility for organizational wide occurrence reporting system; analyze and report trends and identifies appropriate interventions to reduce risk and liability to the organization.</li><li>You will lead organizational performance efforts for JCAHO, core quality measures, COP and regulatory and all other accrediting and regulatory agencies.</li><li>You will ensure compliance with JCAHO, and all legal, regulatory and accrediting agency requirements are met.</li></ul><h6 class="jobSectionHeader">
What qualifications you will need:</h6><ul><li>Bachelor's Degree required in Nursing or Healthcare related field required; Master's Degree preferred</li><li>Current Florida licensure as a Registered Nurse preferred</li></ul>
**If serving as facility&rsquo;s primary Risk Manager, VP must have current Florida license in Healthcare Risk Management (FL LHRM)<ul><li>CPHQ (Certified Professional in Healthcare Quality) OR CHCQM (Diplomate in American Board of Quality Assurance and Utilization Review Physicians)</li></ul>
Individuals without CPHQ or ABQUARP will be granted a 12 month grace period to obtain CPHQ or ABQAURP , if all other qualifications are met<ul><li>CPPS (Certified Professional in Patient Safety) preferred</li><li>Minimum 5 years of experience</li><li>Knowledge of State, Federal, and TJC regulations.</li><li>Previous experience in the clinical, risk management, and/or administrative arenas preferred
</li></ul>For over 40 years, HCA Florida South Tampa Hospital has been providing comprehensive healthcare services. We provide high-quality medical care. We also provide surgery, outpatient therapies, and acute care. With a team of skilled colleagues, it's no wonder we have a reputation for excellence. The over 180-bed acute care hospital is accredited by the Joint Commission. We provide 24-hour Emergency Care, Behavioral Healthcare, and Cardiovascular Services. We also provide General Surgery and Imaging &amp; Diagnostic Services. As South Tampa Hospital and ER, we provide high quality, advanced care. We are one of the best-performing hospitals in the Tampa Bay area. We believe excellent people make excellence happen. If this sounds like the type of meaningful work you'd like to be a part of, we hope you'll consider our careers at South Tampa Hospital.
HCA Healthcare has been named one of the World's Most Ethical Companies by Ethisphere Institute for ten consecutive years (2010-2019). In 2019, HCA Healthcare spent an estimated $3.7 billion in cost for the delivery of charitable care, uninsured discounts, and other uncompensated expenses. 
&quot;Bricks and mortar do not make a hospital. People do.&quot;- Dr. Thomas Frist, Sr. 
HCA Healthcare Co-Founder
If you're looking for a leadership opportunity that provides both personal satisfaction and professional growth, apply to join HCA Healthcare as a(an) VP of Quality and Patient Safety.Unlock your leadership potential with HCA Healthcare.
We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.</div>

VP of Quality and Patient Safety

PRN Clinical Research Infusion Registered Nurse (RN)Location: Tampa, FL Position Type: PRN / Per-Diem (up to 20 hours per week) Reports To: Site DirectorJob Summary&middot; The PRN Infusion Registered Nurse at Axiom Brain Health supports the conduct of clinical research studies by safely administering investigational medications and monitoring participants during and after treatment procedures.&middot; Works closely with the clinical research team to ensure protocol adherence, participant safety, and compliance with Good Clinical Practice (GCP) and applicable regulatory requirements.&middot; Primarily supports infusion and injection visits for clinical trials focused on neurodegenerative and neurologic diseases, including Alzheimer&rsquo;s disease and related conditions.&middot; Helps ensure that study participants receive safe, high-quality care during medication administration and observation periods.Key Responsibilities&middot; Review and maintain all training required to perform clinical trial work including but not limited to Good Clinical Practice (GCP), Human Subject Protection (HSP) and any study related requirements such as the protocol, investigator brochure/package insert, and pharmacy manual.&middot; Administer investigational medications according to study protocols and site procedures, including intravenous (IV) infusions and subcutaneous injections.&middot; Perform IV insertion and maintain IV access during infusion visits.&middot; Monitor participants during medication administration and required post-dose observation periods.&middot; Assess for and appropriately respond to infusion or injection reactions, adverse events (AE) and serious adverse events (SAEs) as outlined in the study protocol. Promptly notifying the Principal Investigator, research team, sponsor and regulatory authorities as applicable.&middot; Accurately document medication administration details including but not limited to dose, route, infusion start and stop times, and participant tolerance.&middot; Collaborate with the clinical research team to ensure participant safety and adherence to study protocol requirements.&middot; Assist with clinical procedures such as vital signs, ECGs, and blood draws when additional clinical support is needed.&middot; Communicate participant status and any safety concerns to the Principal Investigator and study team in a timely manner.&middot; Ensure all clinical procedures are performed in accordance with protocol requirements, site SOPs, and Good Clinical Practice guidelines.&middot; Support efficient clinic operations during infusion visits and maintain a professional and supportive environment for study participants and caregivers.Knowledge, Skills, and Abilities&middot; Strong peripheral IV-line placement and infusion therapy skills&middot; Ability to recognize and appropriately respond to infusion reactions or other clinical concerns&middot; Strong attention to detail and ability to document accurately in real time according to ALCOA-C/Good Documentation Practices (GDP)&middot; Excellent communication and interpersonal skills when interacting with participants, caregivers, and research staff&middot; Ability to work independently and collaboratively in a fast-paced clinical research environment&middot; Comfort working with older adults and individuals with cognitive impairmentWork Environment&middot; Outpatient clinical research setting supporting neurology trials&middot; Participants may include individuals with neurodegenerative conditions&middot; Infusion visits typically range from one to two hours with additional observation time depending on protocol requirementsSchedule&middot; PRN position with flexible scheduling based on study visit needs&middot; Up to approximately 20 hours per weekMinimum Qualifications&middot; Active Registered Nurse (RN) license in the state of Florida&middot; Associate&rsquo;s or Bachelor&rsquo;s degree in Nursing&middot; Minimum of two years of clinical nursing experience&middot; Current BLS certificationPreferred Qualifications&middot; Experience administering infusion therapies or biologic medications&middot; Experience in a clinical research setting&middot; Bilingual &ndash; SpanishThe duties above are representative of the nature and level of work assigned and are not necessarily all-inclusive. Pay: $45.00 - $65.00 per hourWork Location: In person

PRN Clinical Research Infusion Registered Nurse (RN)

JOB SUMMARYThe Clinical Research Coordinator at Axiom Brain Health is responsible supporting the coordination, implementation, and day-to-day management of clinical research studies in accordance with Good Clinical Practice (GCP), Institutional Review Board (IRB) approvals, and regulatory requirements. This role ensures protocol compliance oversight, high-quality data collection and participant safety.This position is ideal for someone who is detail-oriented, organized, and interested in contributing to Alzheimer&rsquo;s and other neurodegenerative disease research.RESPONSIBILITIES<ul><li>Coordinates clinical research studies under the guidance of the Site Director and Principal Investigator (PI).</li><li>Reviews study protocols and supports identification of operational needs and study requirements.</li><li>Schedules and conducts participant study visits and performs protocol-required procedures.</li><li>Collects and records study data in accordance with protocol and regulatory requirements.</li><li>Ensures compliance with study protocols, IRB regulations, institutional policies, FDA regulations, and ICH-GCP guidelines.</li><li>Maintains accurate and timely source documentation, case report forms (CRFs), and study files.</li><li>Supports investigational product (IP) accountability in collaboration with pharmacy or designated site staff.</li><li>Conducts informed consent discussions and ensures documentation aligns with ALCOA-C practices.</li><li>Monitors participant safety, documents adverse events, and communicates with the PI and sponsor as needed.</li><li>Performs data entry and resolves queries in electronic data capture (EDC) systems within required timelines.</li><li>Participates in site visits, including site initiation visits (SIVs), monitoring visits, audits, and inspections.</li><li>Identifies protocol deviations and communicates them to appropriate team members.</li><li>Collaborates with investigators, clinical staff, sponsors, CROs, and regulatory personnel.</li><li>Supports participant recruitment and retention through follow-up and engagement efforts.</li></ul>QualificationsKnowledge, Skills, Abilities<ul><li>Basic knowledge of medical terminology</li><li>Strong verbal and written communication skills</li><li>Strong organizational skills and attention to detail</li><li>Ability to manage multiple tasks and prioritize effectively</li><li>Ability to work in a fast-paced environment</li><li>Ability to work collaboratively within a team</li><li>Willingness to accept direction and feedback</li><li>Experience with CTMS and/or ability to learn systems such as RealTime CTMS</li><li>Proficiency with Google Suite, Microsoft Office (Word, Excel, PowerPoint)</li></ul>Required:<ul><li>Bachelor&rsquo;s degree in a health-related or scientific field; or equivalent clinical research experience</li><li>1&ndash;3 years of clinical research experience</li><li>Basic understanding of ICH-GCP and clinical research processes</li><li>Experience supporting study visits, data entry, and documentation</li></ul>Preferred:<ul><li>Master&rsquo;s degree in a health-related or scientific field</li><li>Clinical research certification (e.g., CCRC, CCRP, ACRP-CP)</li><li>Spanish-speaking</li><li>Experience in Alzheimer&rsquo;s disease or other neurodegenerative research</li><li>Exposure to EDC systems and regulatory documentation</li></ul>This role is part of a small, hands-on team, and responsibilities may evolve over time. Willingness to take on additional tasks, pitch in where needed, and support team priorities is essential.Job Type: Full-timePay: $55,000.00 - $70,000.00 per yearBenefits:<ul><li>401(k)</li><li>Dental insurance</li><li>Flexible spending account</li><li>Health insurance</li><li>Health savings account</li><li>Life insurance</li><li>Paid time off</li><li>Professional development assistance</li><li>Retirement plan</li></ul>Application Question(s):<ul><li>Are you authorized to work in the United States? (Required)</li><li>Will you be able to reliably commute to Tampa, Fl 33609 for this job? (Required)</li></ul>Work Location: In person

Clinical Research Coordinator (in-person)

Explore 111+ Vp cancer clinical research in Tampa this May. Find roles across top companies and apply now to boost your career.