clinical research assistant, prn (bilingual, registered nurse)

clinical research coord - psych (full time, days)

clinical research nurse (full time, days)

clinical research assistant, prn Jobs in Miami

clinical research assistant, prn

clinical research assistant, prn (bilingual, registered nurse) Jobs in Miami

clinical research coord - psych (full time, days) Jobs in Miami

clinical research coordinator Jobs in Miami

clinical research coordinator

clinical research nurse (full time, days) Jobs in Miami

clinical research phlebotomist growth to crc

Integrity Clinical Research

<p><b>Job Overview</b></p><p>We are seeking a dependable and detail-oriented Clinical Research Phlebotomist to join our growing clinical research team.</p><p>This position will begin with a primary focus on phlebotomy and laboratory procedures for approximately 90 days due to maternity coverage. After successful completion of this period, the role will transition into a Clinical Research Coordinator (CRC) position with expanded responsibilities.</p><p>This is a long-term opportunity for candidates interested in building a career in clinical research.</p><p><b>Responsibilities</b></p><p>Phase 1: Phlebotomy &amp; Lab Operations (First 90 Days)</p><ul><li>Perform venipuncture and timed PK blood draws</li><li>Process, centrifuge, aliquot, and prepare specimens per protocol</li><li>Maintain accurate and timely documentation</li><li>Ensure compliance with lab manuals and protocol requirements</li><li>Monitor specimen storage and shipping requirements</li><li>Assist with patient intake and vital signs</li></ul><p>Phase 2: Clinical Research Coordinator Duties</p><ul><li>Coordinate study visits and patient scheduling</li><li>Conduct informed consent process</li><li>Document and report adverse events (AE/SAE)</li><li>Maintain regulatory binders and source documentation</li><li>Communicate with sponsors and monitors</li><li>Ensure strict adherence to study protocols and timelines</li></ul><p><b>Required Skills &amp; Qualifications</b></p><ul><li>Minimum 1 year phlebotomy experience</li><li>Comfortable performing multiple blood draws daily</li><li>Strong attention to detail and documentation accuracy</li><li>Ability to follow strict protocol timelines</li><li>Professional communication skills</li><li>Ability to work in a fast-paced clinical environment</li></ul><p>Preferred:</p><ul><li>Clinical research experience</li><li>Medical Assistant certification</li><li>GCP training</li><li>Bilingual (English/Spanish)</li></ul><p><b>Who This Role Is Ideal For</b></p><ul><li>Medical Assistants looking to grow into research</li><li>Entry-level CRCs seeking hands-on experience</li><li>Foreign Medical Graduates seeking U.S. research experience</li><li>Candidates interested in long-term clinical research careers</li></ul><p>Pay: $18.00 - $19.00 per hour</p><p>Work Location: In person</p>

Clinical Research Phlebotomist (Growth to CRC)

Nicklaus Children's Health System

<div><h2 class="jobSectionHeader"><div><b>Description</b></div></h2><p><b>
Job Summary</b></p>
<p>
Under direction of the Senior Manager of Clinical Trial Operations, the Clinical Research Coordinator (CRC) CTO manages and conducts the day-to-day activities of a research study. In general, the CRC ensures the study maintains in accordance with the protocol, applicable regulations, and Good Clinical Practice (GCP) and Institutional Review Board (IRB) requirements. Beyond administrative duties, responsibilities of a CRC 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.</p>
<p><b>
Job Specific Duties</b></p>
<ul>
<li>Attends and participates in investigator meetings, pre-study visits, and initiation meetings or coordinator meetings as appropriate.<br>
</li>
<li>Collects and maintains accurate patient data for submission to Sponsor, maintaining proper patient records, coordinating the collection, and shipments of specimens as required by protocol.<br>
</li>
<li>Communicates study objectives/procedures to relevant hospital units involved with the study including the establishment of good rapport with the Principal Investigator &amp; providing required assistance.<br>
</li>
<li>Communicates with the Sponsor or their representatives, schedules and facilitates study monitor visits, and facilitates communication between Principal Investigator and Sponsor or Sponsor&rsquo;s Representatives.<br>
</li>
<li>Complies with the Research Finance Compliance policies and procedures including reporting requirements to research finance staff.<br>
</li>
<li>Interacts with patients and families to recruit (screen, consent, and enroll) study subjects and ensures compliance with the protocol.<br>
</li>
<li>Responsible for speedy and adequate patient enrollment as determined by Research Management and Principal Investigator in all assigned studies.<br>
</li>
<li>Demonstrates and utilizes Good Clinical Practices in the conduct of clinical trials as per established protocol.<br>
</li>
<li>Follows NCRI&rsquo;s Standard Operating Procedures, AAHRPP, HIPAA, and FDA guidelines for clinical research, and keeps updated in those procedures and/or guidelines.<br>
</li>
<li>Enters required data into CTMS in a timely manner, as stablished in department procedures.
<br>
</li><li>Provides new Protocols, Amendments, and study status updates to necessary research staff for digitization/entry into CTMS.<br>
</li>
<li>Keeps electronic patient files and required documents up-to-date within e-regulatory system.</li>
<li>Collaborates with study investigators to pre-screen and recruit patients to available clinical trials.</li>
</ul><h2 class="jobSectionHeader"><div><b>Qualifications</b></div></h2>
<ul><li></li></ul><p><b>
** Position is onsite in Miami **</b></p><p><b>
Minimum Job Requirements</b></p><ul><li>
Bachelor's degree and previous research experience (OR) Associate's degree and 2 years of research experience (OR) 3 years of research experience (OR) 5 years of healthcare experience</li></ul><p><b>
Knowledge, Skills, and Abilities</b></p><ul><li>
Experience in pediatric clinical research in a hospital setting highly preferred.<br>
</li><li>
Experience with relevant hospital equipment for each clinical trial project.<br>
</li><li>
Bilingual in English/Spanish preferred.<br>
</li><li>
Clinical research certification (CCRC, CCRP, CRA) and IATA certification preferred.<br>
</li><li>
Excellent communication skills in working with both children and adults.<br>
</li><li>
Excellent organizational skills, detail-oriented, people-oriented, flexible, and adaptable to change.<br>
</li><li>
Excellent time management skills.<br>
</li><li>
Knowledge of protocols and its process.<br>
</li><li>
Experience with software applications including word processing, scheduling and contact database, email, web browsing, hospital records, other database software and office equipment.<br>
</li><li>
Availability to work adjusted hours to accommodate subject visits.</li></ul><br>
<br>
<br>
<h2 class="jobSectionHeader"><div><b>Job:</b></div></h2>
Research<br>
<h2 class="jobSectionHeader"><div><b>
Department:</b></div></h2>
RI - ADMINISTRATION-2100-380950<br>
<h2 class="jobSectionHeader"><div><b>
Job Status:</b></div></h2>
Full Time</div>

Clinical Research Coord - Psych (Full Time, Days)

<div><h2 class="jobSectionHeader"><div><b>Description</b></div></h2><p><b>
Job Summary</b></p>
<p>
The Clinical Research Nurse, CTO is part of a central team of specialized research professionals within the Nicklaus Children's Hospital Research Institute (NCH-RI). This research position reports directly to the NCH-RI Clinical Trials Office (CTO) Manager but works closely with Lead CRA's, Study Team (PI, Sub-I's, CRC', etc.), NCH-RI departments and Nicklaus Children's 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. This research position will also coordinate team activities to ensure studies are carried out according to protocol, standard operating procedures (SOPs) and applicable guidelines and regulations.</p>
<p><b>
Job Specific Duties</b></p>
<ul>
<li>Coordinates team activities to ensure studies are carried out according to protocol, standard operating procedures (SOPs) applicable guidelines and regulations, and within budget.<br>
</li>
<li>Plans logistical activity for procedures as per protocol and ensures thorough resource planning. Identifies risks on study and ensures that actions are implemented to mitigate risks identified.<br>
</li>
<li>Ensures study specific training materials, documents, and records are prepared and delivered or coordinate training, dry runs, simulations and tests as required.<br>
</li>
<li>Implements, monitors, and assesses the need for training programs to maintain staff skill proficiency, including annual validation and currency of required certifications and licenses.<br>
</li>
<li>Provides protocol-specific training to research study team and NCH hospital/department staff directly involved with the care/treatment of research patients.<br>
</li>
<li>Works with NCH-RI staff to assist with developing, updating and implementing new Research Standard Operating Procedures, guidance documents, standard work and work flows (related to early phase research).<br>
</li>
<li>Coordinates, plans, implements, and evaluates nursing care to clinical trial study participants including but not limited to Adverse Event reporting and other support activities.<br>
</li>
<li>Provides nursing-related care to clinical trial study participants as outlined (and applicable) in the study protocol.<br>
</li>
<li>Coordinates and executes the collection, compilation, and analysis of clinical research data from studies conducted by PIs and study teams at Nicklaus Children&rsquo;s and the NCH-RI.<br>
</li>
<li>Interacts with patients and families to recruit study subjects and ensures compliance with protocol guidelines and requirements of regulatory agencies.<br>
</li>
<li>Attends and participates in investigator meetings, pre-study visits/initiation or coordinator meetings. Produces quality documentation, including completion of assessments within the specified time.<br>
</li>
<li>Coordinates and responsible for the collection of blood samples (PK samples and other), cultures, tissues and other specimens as required by protocol.<br>
</li>
<li>Prepares oral presentations/written reports/data requests describing progress, trends and appropriate recommendations or conclusions as it relates to research at Nicklaus.
<br>
</li><li>Communicates with the Sponsor or representatives regarding scheduling and facilitation of study monitor visits and facilitates communication between PI and Sponsor or Sponsor&rsquo;s Representatives.<br>
</li>
<li>Reviews protocol and provides study feasibility input to the NCH-RI Leadership and Study Start-up Team. Works with QI/QA team to ensure quality standards are being met and reports adverse events, protocol deviations.<br>
</li>
<li>Ensures compliance of general and study specific regulatory related processes with SOPs, FDA, NIH, and applicable regulations for the reporting of events to regulatory agencies.<br>
</li>
<li>Assists with the design and implementation of protocols, forms/questionnaires and the preparation of amendments to protocols and/or modifications to study design as appropriate for local, Investigator Initiated studies.</li>
</ul><h2 class="jobSectionHeader"><div><b>Qualifications</b></div></h2>
<p><b>Minimum Job Requirements</b></p>
<ul>
<li>BSN &ndash; Bachelors of Science in Nursing<br>
</li>
<li>RN Licensure within the State of Florida or Multi-State Enhanced Nursing License Compact (eNLC) &ndash; maintain active and in good standing throughout employment<br>
</li>
<li>IATA certification completion required within 3 months of hire date<br>
</li>
<li>American Heart Association ACLS (Advanced Cardiovascular Life Support) certification required within 2 months of hire<br>
</li>
<li>American Heart Association PALS (Pediatric Advanced Life Support) certification completion required within 6 months of hire<br>
</li>
<li>American Heart Association BLS - maintain active and in good standing throughout employment<br>
</li>
<li>2-4 years of professional research or healthcare experience<br>
</li>
<li>1-3 years of Phase 1 clinical research experience</li>
</ul>
<p><b>Knowledge, Skills, and Abilities</b></p>
<ul>
<li>ARNP highly preferred<br>
</li>
<li>Clinical research certification (e.g., CCRC, CCRP, CRA) preferred<br>
</li>
<li>Bilingual in English/Spanish preferred<br>
</li>
<li>Pediatric Nursing experience in an acute care setting preferred<br>
</li>
<li>Experience in neurology, neurosurgery, or oncology preferred<br>
</li>
<li>Experienced with database management tools and/or REDCap preferred<br>
</li>
<li>In-depth knowledge of Phase I clinical trials<br>
</li>
<li>Demonstrated knowledge of clinical research trial design and execution<br>
</li>
<li>Experienced with electronic medical record and clinical trial management software applications<br>
</li>
<li>Strong written and verbal communication skills<br>
</li>
<li>Excellent interpersonal skills<br>
</li>
<li>Excellent problem-solving skills<br>
</li>
<li>Effective organizational and project management skills<br>
</li>
<li>Ability to pay close attention to detail<br>
</li>
<li>Ability to comprehend professional and scientific journals<br>
</li>
<li>Ability to apply principles of logical and scientific thinking to a wide variety of intellectual and practical problems<br>
</li>
<li>Ability to establish and maintain effective working relationships with coworkers, managers and clients<br>
</li>
<li>Proficiency in Microsoft Office including Access, Word, Excel, Outlook, and PowerPoint<br>
</li>
<li>Willing to work off-hours depending on the study requirements</li></ul><br>
<div></div>
<br>
<br>
<h2 class="jobSectionHeader"><div><b>Job:</b></div></h2>
Research<br>
<h2 class="jobSectionHeader"><div><b>
Department:</b></div></h2>
RI - ADMINISTRATION-2100-380950<br>
<h2 class="jobSectionHeader"><div><b>
Job Status:</b></div></h2>
Full Time</div>

Clinical Research Nurse (Full Time, Days)

Leon Medical Centers

<div><div><div><p><b>Medical Assistant</b></p><p><b>
Location:</b> Kendall Center - 12515 SW 88th St Miami, FL 33186</p><p><b>
Employment Type:</b> Full-time</p><p><b>
About Us:</b></p><p>
Thank you for your interest in pursuing an employment opportunity with Leon Medical Centers. Our fast-growing company employs over 2,500 professionals dedicated to serving over 40,000 patients. Leon Medical Centers is the first organization to serve as an educational and research center. It has been named one of the top four medical institutions in the nation, received multiple awards for its medical excellence, and is an academic center affiliated with the Benjamin Leon School of Nursing at Miami Dade College, the University of Miami Jackson Memorial Hospital Geriatric Fellowship program, and Florida International University's Herbert Wertheim College of Medicine.</p><p>
If you are searching for a fulfilling career in a healthcare organization that improves lives daily, this position is for you.</p><p><b>
Position Summary:</b></p><p>
A Medical Assistant carries out a range of clinical and administrative duties in an outpatient examination room while supervised by a physician.</p><p><b>
Responsibilities:</b></p><ul><li>
Taking patient's vital signs and inputting patient information into our ERM system</li><li>
Preparing patients for any necessary examination</li><li>
Cleaning and disinfecting treatment spaces</li><li>
Complying with LMC's infection control policies and procedures</li></ul></div><div><div><div><b>
Be part of an award-winning team!</b></div></div><div><b>
Please click on &quot;</b><b>Apply Online</b><b>&quot; </b><b>to submit your employment application.</b></div><div><b>
Please complete the application fully.</b></div></div></div><div><p><b>
Requirements:</b></p><ul><li><b>
Medical Assistant and Phlebotomy Certifications</b> obtained from an accredited provider.</li><li><b>
Cardiopulmonary resuscitation (CPR) or Basic Life Support (BLS) certification</b> for healthcare providers issued by the American Red Cross or American Heart Association.</li><li><b>
Fluency in English and Spanish</b> is required in order to communicate effectively with our patient population.</li><li>
Minimum of 1 year of experience as a Medical Assistant, Phlebotomist, or in additional areas of patient health care in a clinical setting.</li><li>
A High School Diploma or equivalent</li></ul><p><b>
Skills:</b></p><ul><li>
Excellent verbal and written communication skills.</li><li>
Ability to work effectively independently and in a team environment.</li></ul></div></div>

Medical Assistant

Labcorp

<div><h2 class="jobSectionHeader"><b>LabCorp is seeking a Phlebotomist to join our team at University of Miami Health in Miami, FL</b></h2><p></p><p><b>
Work Schedule: </b>Monday - Friday 9:30am - 6:00pm and rotating Saturdays</p><p></p><p><b>
Job Responsibilities:</b></p><ul><li>
Perform blood collections by venipuncture and capillary techniques for all age groups</li><li>
Collect specimens for drug screens, paternity tests, alcohol tests etc.</li><li>
Perform data entry of patient information in an accurate and timely manner</li><li>
Process billing information and collect payments when required</li><li>
Prepare all collected specimens for testing and analysis</li><li>
Maintain patient and specimen information logs</li><li>
Provide superior customer service to all patients</li><li>
Administrative and clerical duties as necessary</li><li>
Travel to additional sites when needed</li></ul><p></p><p><b>
Minimum Qualifications:</b></p><ul><li><p>
High school diploma or equivalent</p></li></ul><p></p><p><b>
Preferred Qualifications:</b></p><ul><li><p>
1 year phlebotomy experience working with cancer patients</p></li></ul><p></p><p><b>
Additional Job Standards:</b></p><ul><li>
Phlebotomy certification or completed training program from an accredited agency or 3 months experience as a phlebotomist</li><li>
Proven track record in providing exceptional customer service</li><li>
Strong communication skills; both written and verbal</li><li>
Ability to work independently or in a team environment</li><li>
Comfortable working under minimal supervision</li><li>
Reliable transportation required</li><li>
Flexibility to work overtime as needed</li><li>
Able to pass a standardized color blindness test</li></ul><p></p><p><b>
At LabCorp we have a passion in helping people live happy and healthy lives. Every day we provide vital information that helps our clients and patients understand their health. If you are passionate about helping people and have a drive for service, then LabCorp could be a great next career step!</b></p><p></p><p><b>
We are currently seeking a Phlebotomist to work at Sylvester Comprehensive Cancer Center. In this role you will provide exceptional customer service, perform skilled specimen collections and be the face of the company. In addition, you will be provided opportunities for continuous growth within the organization.</b></p><p></p><p><b>
All job offers will be based on a candidate&rsquo;s skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data</b></p><p></p><p><b>
Phlebotomist&rsquo;s may be eligible for participation in the PST Incentive Plan, which pays a quarterly bonus based on performance metrics.</b></p><p></p><p><b>
Benefits:</b><b> </b>Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Casual, PRN &amp; Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. Employees who are regularly scheduled to work a 7 on/7 off schedule are eligible to receive all the foregoing benefits except PTO or FTO. For more detailed information, please click here.</p><p></p><p>
If you're looking for a career that offers opportunities for growth, continual development, professional challenge and the chance to make a real difference, apply today!</p><p></p><p><b>
Labcorp is proud to be an Equal Opportunity Employer:</b></p><p>
Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.</p><p></p><p><b>
We encourage all to apply</b></p><p>
If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement.</p></div><p></p>

Phlebotomist

Centrum Health

<div><div><p><b>WHO WE ARE</b></p>
<p>
NeueHealth is a value-driven healthcare company grounded in the belief that all health consumers are entitled to high-quality, coordinated care. By uniquely aligning the interests of health consumers, providers, and payors, we help to make healthcare accessible and affordable to all populations across the ACA Marketplace, Medicare, and Medicaid.</p>
<p>
NeueHealth delivers clinical care to health consumers through our owned clinics &ndash; Centrum Health and Premier Medical &ndash; as well as unique partnerships with affiliated providers across the country. We also enable providers to succeed in performance-based arrangements through a suite of technology and services scaled centrally and deployed locally. Through our value-driven, consumer-centric approach, we are committed to transforming healthcare and creating a better care experience for all.</p></div><div><b>
JOB SUMMARY</b></div>
<div>Perform administrative and certain clinical duties under the direction of a physician. Administrative duties may include scheduling appointments and maintaining medical records. Clinical duties may include taking and recording vital signs and medical histories, preparing patients for examination, drawing blood, and administering medications as directed by physician.</div>
<div></div>
<div><b>DUTIES &amp; RESPONSIBILITIES</b></div>
<div>The Medical Assistant job description is intended to highlight major responsibilities within the role, but it is not limited to these items.</div>
<ul><li>Taking Patient Vital Signs</li>
<li>Taking Medical Histories</li>
<li>Preparing Patients for Medical Tests and Examinations</li>
<li>Assisting Physicians During Examinations</li>
<li>Explaining Medical Procedures to Patients</li>
<li>Sterilizing Medical Instruments</li>
<li>Removing Sutures</li>
<li>Calling or electronic entering Prescriptions into Pharmacies</li>
<li>Preparing Patients for X-Rays</li>
<li>Administering Topical, Oral, or Intramuscular Medications</li>
<li>Transcribing all notes and documents related to treatments.</li>
<li>Other duties as assigned</li>
<li>Travel to clinics within the region as needed for business operation or staffing coverage requirements.</li></ul><p><br>
</p><div><b>EDUCATION AND PROFESSIONAL EXPERIENCE</b></div>
<ul><li>High School Diploma or GED equivalent</li>
<li>Certification as a Medical Assistant or diploma from an accredited school is highly preferred.</li>
<li>A minimum of one year experience as a Medical Assistant in a clinic, physician practice or urgent care setting</li></ul><br>
<p></p>
<div><b>
PROFESSIONAL COMPETENCIES</b></div>
<ul><li>Strong knowledge of medical correspondence, managing electronic medical records</li>
<li>Excellent customer service skills</li>
<li>Experience as a Phlebotomist is desirable but not required.</li>
<li>Excellent verbal and written communication skills</li>
<li>Team player, able to work with provider and other team members of the care team.</li>
<li>Bilingual (English and Spanish) preferred</li>
</ul><div><div>As an Equal Opportunity Employer, we welcome and employ a diverse employee group committed to meeting the needs of NeueHealth, our consumers, and the communities we serve. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, national origin, protected veteran status, disability status, sexual orientation, gender identity or expression, marital status, genetic information, or any other characteristic protected by law.</div></div></div>

Medical Assistant - Little Havana

Airport Medical Clinic

<p><b>Overview</b><br/>We are seeking a dynamic and experienced Medical Director to lead our clinical operations and ensure the highest standards of patient care, medical management, and healthcare quality. In this pivotal role, you will oversee clinical protocols, collaborate with multidisciplinary teams, and drive initiatives aligned with regulatory standards. Your leadership will shape the strategic direction of our healthcare services, fostering innovation and excellence across all clinical activities. This position offers an exciting opportunity to influence patient outcomes while maintaining compliance with industry regulations and standards. <b>Pay will be based on experience</b> .</p><p><b>Responsibilities</b></p><ul><li>Provide expert medical leadership across all clinical programs, ensuring adherence to healthcare regulations such as HIPAA, FDA regulations, and NCQA standards.</li><li>Develop, review, and implement clinical policies and procedures aligned with best practices in healthcare management.</li><li>Oversee utilization management processes to optimize patient care pathways and resource allocation.</li><li>Supervise medical staff, including physicians, nurses, and allied health professionals, fostering a collaborative environment focused on quality improvement.</li><li>Ensure accurate documentation within electronic health record (EHR) systems and medical records management in compliance with HIPAA privacy rules.</li><li>Lead clinical research initiatives to advance evidence-based practices and support product or service development.</li><li>Collaborate with hospital administration on budgeting, resource planning, and strategic growth initiatives related to clinical services.</li><li>Maintain up-to-date knowledge of physiology, anatomy, and medical terminology to guide clinical decision-making effectively.</li></ul><p><b>Qualifications</b></p><ul><li>Medical degree (MD or DO) from an accredited institution with active medical licensure.</li><li>Extensive experience in healthcare management within hospital settings or managed care organizations.</li><li>Proven leadership skills with supervising experience in clinical environments.</li><li>Strong knowledge of EMR systems, EHR systems, and medical records management.</li><li>Familiarity with FDA regulations, NCQA standards, HIPAA compliance, and utilization management protocols.</li><li>Demonstrated expertise in clinical research, medical development processes, and healthcare policy adherence.</li><li>Excellent project management skills with the ability to coordinate multiple initiatives simultaneously.</li><li>Deep understanding of physiology, anatomy, and medical terminology essential for effective oversight of patient care processes. Join us as a Medical Director to lead transformative healthcare initiatives that improve patient outcomes while ensuring compliance with industry standards. Your expertise will inspire teams to deliver exceptional care in a fast-paced environment committed to innovation and excellence.</li></ul><p>Job Type: Part-time</p><p>Work Location: In person</p>

Medical Director

Explore 483+ Clinical research phlebotomist growth to crc in Miami this March. Find roles across top companies and apply now to boost your career.