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Headlands Research

<div><div>At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.</div> 


 Rolling Hills Estates, CA 
 Peninsula Research Associates (a Headlands Research site) 
 Full-Time Temporary (3 months with potential to turn into permanent role) | Monday through Friday | Onsite (no opportunities for hybrid or remote)
<h3 class="jobSectionHeader">
For experienced CRCs looking for stability, collaboration, and meaningful work</h3>

If you're an experienced Clinical Research Coordinator I, II, or III who values strong operations, multidisciplinary collaboration, and a schedule that actually supports work&ndash;life balance, Peninsula Research Associates may be the right next step in your career.

Our Rolling Hills Estates site is known for its depth of experience, thoughtful study execution, and team-based approach to clinical research&mdash;particularly in vaccines, immunology and allergy studies. 


<h2 class="jobSectionHeader">About Peninsula Research Associates</h2>

Peninsula Research Associates (PRA) is dedicated to advancing medical treatments through the use of innovative techniques and increasing awareness. PRA has achieved significant study results in allergy, asthma, vaccines, otitis media and sinusitis treatment and has earned a reputation for conducting quality research. 


<h2 class="jobSectionHeader">Why Experienced CRCs Choose PRA</h2>
<ul><li>Multi-disciplinary collaboration with seasoned investigators and clinical staff</li>
<li>Strong operational support and clear SOPs</li>
<li>Exposure to complex, meaningful studies&mdash;not just high-volume turnover</li>
<li>A site with long-standing credibility and research maturity</li>
<li>Backing of a growing research network with resources and stability</li>
</ul>
This role is ideal for CRCs who enjoy owning their studies, working with competent teams, and being trusted to execute with precision. 


<h2 class="jobSectionHeader">What You'll Do</h2>
<ul><li>Coordinate all aspects of assigned clinical trials from site initiation through close-out</li>
<li>Conduct subject visits and ensure accurate, timely documentation in compliance with ALCOA-C standards</li>
<li>Maintain compliance with protocols, GCP/ICH guidelines, FDA regulations, IRB requirements, and SOPs</li>
<li>Manage subject recruitment, informed consent, and retention activities</li>
<li>Ensure timely EDC data entry and resolution of queries</li>
<li>Report and follow up on AEs, SAEs, and protocol deviations</li>
<li>Collaborate with investigators, sponsors/CROs, labs, and internal teams</li>
<li>Prepare for and participate in monitoring visits, audits, and inspections</li>
<li>Maintain regulatory documentation and ensure training compliance for amendments and systems</li>
<li>Perform study procedures such as phlebotomy, ECGs, and sample processing (as trained)</li>
<li>Attend investigator meetings and provide cross-functional support as needed</li>
<li>Maintain working knowledge of protocols, lab manuals, equipment calibration, and inventory</li></ul> 


<h2 class="jobSectionHeader">What We're Looking For</h2>
<ul><li>High school diploma or GED required; Bachelor's degree preferred</li>
<li>At least one year of experience coordinating Phase 2&ndash;4 industry-sponsored clinical trials</li>
<li>Strong understanding of FDA regulations, ICH-GCP, and clinical trial operations</li>
<li>Experience with EDC, IVRS, and clinical research platforms</li>
<li>Proficiency in medical terminology and clinical documentation</li>
<li>Strong organizational skills with the ability to manage multiple studies</li>
<li>Clear, professional verbal and written communication skills</li>
<li>Comfortable working onsite in a collaborative, clinical environment</li></ul> 


<h2 class="jobSectionHeader">Who Thrives in This Role</h2>
<ul><li>CRCs who want structure, support, and accountability</li>
<li>Professionals who value teamwork over silos</li>
<li>Coordinators who care about data quality, patient experience, and compliance</li>
<li>Those ready to grow within a stable, well-established research site</li></ul> 


 Apply today if you're looking for a CRC role where your experience is respected, your schedule is predictable, and your work directly contributes to advancing meaningful medical research.</div>

Temporary Clinical Research Coordinator I, II, or III

Valley Foot and Ankle Inc

About Us Statera Research is a leading clinical research network dedicated to advancing innovation in wound care, diabetic foot ulcers, and regenerative medicine. Our collaborative model brings together experienced investigators, research professionals, and healthcare providers to ensure the highest standards of quality, compliance, and patient care across our active clinical trials.Position Summary The Clinical Research Coordinator (CRC) is responsible for the daily management and conduct of clinical research studies in accordance with FDA, GCP, and ICH guidelines. The CRC will work closely with the Principal Investigator and clinical team to ensure protocol compliance, subject safety, and accurate data collection.Key Responsibilities &middot; Coordinate all aspects of clinical trials from site initiation to close-out. &middot; Screen, consent, and enroll study participants per protocol and IRB requirements. &middot; Maintain accurate and timely source documentation, eCRF entry, and regulatory binders. &middot; Schedule and conduct study visits, assessments, and follow-ups. &middot; Manage investigational product accountability, temperature logs, and shipping records. &middot; Communicate with sponsors, monitors, and CROs during monitoring visits and audits. &middot; Assist with regulatory submissions, IRB correspondence, and protocol amendments. &middot; Participate in investigator meetings, staff training, and internal quality reviews.Qualifications &middot; Certified or experienced Medical Assistant (MA, CMA, or RMA) required. &middot; Prior experience in a medical office, wound care, or podiatry clinic preferred. &middot; Interest in or exposure to clinical research (training provided). &middot; Strong attention to detail, organizational, and documentation skills. &middot; Excellent interpersonal and communication abilities. &middot; Proficient in Microsoft Office, EMR systems, and basic data entry. &middot; CPR certification preferred. Job Type: Full-time Pay: From $18.00 per hour Expected hours: 40 per week Please feel free to reach out with any further questions, my cell is_ 619-647-5750_.Job Type: ContractPay: $18.00 - $22.00 per hourWork Location: Hybrid remote in Los Angeles, CA

Clinical Research Coordinator - LOS ANGELES LOCAL ONLY - INDEPENDENT CONTRACTOR

Children's Hospital Los Angeles

<div>Location/Org Data : Introduction:
<div>
Join a team that's shaping the future of pediatric care. Children&rsquo;s Hospital Los Angeles is consistently ranked among the top 10 children's hospitals in the nation, delivering world-class care through more than 350 specialized programs and services. Here, world-class experts in medicine, research, and education work together to deliver family-centered care to more than 155,000 patients each year. At CHLA, your work will help build brighter tomorrows for the children and families we serve.</div>
Overview:
<div>
Schedule: Monday-Friday 9:00am-5:30pm Hybrid</div><div></div><div> 
Purpose Statement/Position Summary: The Coordinator, Clinical Trial Operations (Coordinator, CTO) must have a broad spectrum of knowledge and experience in conducting multi-center clinical and research studies. The individual should be able to work independently to coordinate and manage consortium activities at the central operations center, with guidance from the appointed consortium leaders (e.g., Consortium Medical Director, Associate Medical Director, Administrative Director, etc.). The Coordinator, CTO will be the main contact for consortium participating sites and assist with all assigned protocol related matters such as regulatory compliance requirements (e.g. FDA, IRB, etc.), eCRF database configuration, system access management, operational requirements (e.g. eCRF completion guidelines, SOPs, etc.), and other activities required for member sites to participate in consortium clinical and research studies. The individual must be detail oriented, have the ability to prioritize, be able to multitask, possess critical thinking skills, and can analyze/troubleshoot issues as they arise. The individual must have excellent organization skills to efficiently review and maintain operational and study related records. Additionally, the individual must have the interpersonal skills necessary to work effectively with external participating sites, ancillary staff &amp; research teams. They must have great command of English language (professionally spoken &amp; written) and the ability to deliver accurate information via phone and e-mail.</div><div></div><div> 
Minimum Qualifications/Work Experience: Minimum of 4 years of experience in Phase I-III clinical trials with focus on multi-center trials in oncology. Clinical trial experience includes but is not limited to study protocol development, regulatory maintenance, and reporting (e.g., SAEs, IRB submissions, etc.), eCRF development, data management, and coordination of investigational product. IDE/IND submission experience preferred.</div><div></div><div> 
Education/Licensure/Certification: Bachelor&rsquo;s Degree required (RN Degree is preferred), Masters preferred. SoCRA or ACRP Certification is required within 6 months of hire. Strong computer skills with proficiency in Word, Excel, PowerPoint, etc.</div>
Pay Scale Information: CHLA values the contribution each Team Member brings to our organization. Final determination of a successful candidate&rsquo;s starting pay will vary based on a number of factors, including, but not limited to, education and experience within the job or the industry. The pay scale listed for this position is generally for candidates who meet the specified qualifications and requirements listed on this specific job description. Additional pay may be determined for those candidates who exceed these specified qualifications and requirements. We provide a competitive compensation package that recognizes your experience, credentials, and education alongside a robust benefits program to meet your needs. Posting Range: $70,304.00-$99,341.00 Location/Org Data : Closing:
<div>
CHLA is a leader in pediatric and adolescent health, in our community, across the nation, and around the world . As a premier Magnet&reg;-recognized teaching hospital, CHLA offers an environment rooted in learning, collaboration, and compassionate care. . We are home to groundbreaking research, clinical innovation, and a culture that supports personal and professional growth.</div><div>
Since 1932, CHLA has been affiliated with the Keck School of Medicine of the University of Southern California. Through this partnership and our own enduring mission, we remain committed to creating hope and building healthier futures.</div></div>

Coordinator, Clinical Trial Operations

Cedars-Sinai

<div>
 
 Job Description
 
 
 
 The Smidt Heart Institute reflects Cedars-Sinai's steadfast dedication to heart disease and research innovation giving patients access to the highest level of care. Year after year, thousands of people trust their hearts to Smidt Heart Institute at Cedars-Sinai. Our cardiologists, cardiac surgeons and specialized care teams treat the full spectrum of heart disease and disorders, while our investigators continue to advance the field with groundbreaking, life-saving research. From genetic counseling and targeted drug therapies to a growing array of minimally invasive procedures, Cedars-Sinai continues to stand at the forefront of technology, innovation and discovery improving patient outcomes.
 
 
 
 Join our team and use your skill with an organization known nationally for excellence in research!
 
 
 
 
 Job Summary:
 
 
 
 The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. This role evaluates and abstracts research data and ensures compliance with protocol and research objectives. Position is responsible for completing case report forms, entering clinical research data, and assist with regulatory submissions to the IRB. Provides limited patient contact as needed for study and assist with study budget and patient research billing. This role will comply with all federal, local, FDA, IRB, and HIPAA guidelines and regulations pertaining to the study and patient care.
 
 
 
 Job Duties and Responsibilities:
 
 
 
 Works with a Clinical Research Coordinator, Research Program Administrator or Research Nurse to coordinate/implement study.
 
 
 Evaluates and abstracts clinical research data from source documents.
 
 
 Ensures compliance with protocol and overall clinical research objectives.
 
 
 Completes Case Report Forms (CRFs).
 
 
 Enters clinical research data into Electronic Data Systems (EDCs) that are provided by the sponsors.
 
 
 Provides supervised patient contact or patient contact for long term follow-up patients only.
 
 
 Assists with regulatory submissions to the Institutional Review Board (IRB) and works closely with supervising research staff or directly with the Institutional Review Board to submit Adverse Events, Serious Adverse Events, and Safety Letters in accordance with local and federal guidelines.
 
 
 Assists with clinical trial budgets and patient research billing as needed
 
 
 Schedules patients for research visits and research procedures.
 
 
 Responsible for sample preparation and shipping and maintenance of study supplies and kits.
 
 
 Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board.
 
 
 Maintains research practices using Good Clinical Practice (GCP) guidelines.
 
 
 Maintains strict patient confidentiality according to HIPAA regulations and applicable law.
 
 
 Participates in required training and education programs.
 
 
 
 Qualifications
 
 
 
 
 Education:
 
 
 
 High School diploma/GED required.
 
 
 BA/BS degree in Science, Sociology or related degree preferred.
 
 
 
 Experience:
 
 
 
 Understanding of general research objectives.
 
 
 
 1 Year Of Clinical Research Related Experience Preferred.
 
 
 
 <ul>
 <li>
 Excellent language skills and understanding of Grants, Manuscript, and Abstract guidelines.
 </li>
 <li>
 Strong verbal and writing ability as well as communication, computer, organization, personnel and time-management skills.
 </li>
 <li>
 Proficiency in Word, PowerPoint and Excel.
 </li>
 <li>
 Ability to work independently, set priorities, and handle multiple tasks requiring attention to detail.
 </li>
 <li>
 Previous experience in research environment preferred.
 
 
 </li>
 </ul>
 Physical Demands:
 
 
 <ul>
 <li>
 Able to perform moderate lifting.
 </li>
 <li>
 Able to sit, stand and walk for prolonged periods of time
 </li>
 <li>
 Able to read papers and online documents.
 </li>
 <li>
 Able to operate standard office equipment
 </li>
 <li>
 Able to exercise physical ability and perspective acuity to satisfactorily perform essential job functions.
 </li>
 </ul>
</div>

Heart Institute Clinical Research Associate I - per diem/ Cheng Lab

UCLA Health

<div><div>Description
The Department of Medicine is seeking a highly motivated Program Coordinator to join the UCLA Women&rsquo;s Health Education &amp; Research Center in the General Internal Medicine and Health Services Research Division. As Program Coordinator, you will play a key role in providing administrative support to the Center. You'll manage correspondence, schedule meetings, and prepare reports while also ordering office supplies and materials. In addition, you'll have the opportunity to assist with conference and program planning, including Continuing Medical Education seminars, as well as grant writing and research and evaluation studies. You'll also help maintain and update the website, social media platforms, and the Center&rsquo;s promotional materials, ensuring that the Division&rsquo;s online presence is informative and engaging. This opportunity is ideal for organized, self-starters seeking a dynamic administrative role.
Hourly range: $26.42-$37.49</div><div>
Qualifications
Required:
<ul><li>
Skill in editing for spelling, punctuation, and grammar. Ability to recognize, spell, and use technical and medical terminology appropriately.</li><li>
Typing skills to quickly and accurately prepare documents.</li><li>
Skills in typing numerical tables of data using format provided.</li><li>
Ability to type with speed and accuracy using a PC</li><li>
Skill in proofreading types material and all written works</li><li>
Ability to seek appropriate staff and other resources when questions regarding format, illegible writing, or office procedures arise</li><li>
Ability to use software: MS Word, PowerPoint, Excel,Photoshop, Adobe, Canva</li><li>
Ability to manage Zoom functions.</li><li>
Ability to use photocopy machine and fax machine as needed.</li><li>
Knowledge of University policies and procedures on travel</li><li>
Knowledge of University policies and procedures regarding procurement</li><li>
Demonstrated ability to establish and maintain cooperative working relationships with other staff members and faculty.</li><li>
Skill in setting priorities which accurately reflect relative importance of job responsibilities and in coordinating projects from multiple supervisors</li><li>
Skill in exercising good judgment in dealing with Center visitors</li><li>
Ability to work independently via Zoom and maintain accountability for time and work</li></ul>
Preferred:<ul><li>
Bachelor's Degree Bachelor's Degree and/or equivalent combination of education and experience.</li></ul></div></div>

Program Coordinator

<div><div>At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.</div> 


 Rolling Hills Estates, CA 
 Peninsula Research Associates 
 Full-Time | Mon&ndash;Fri, 8:00am&ndash;5:00pm)
<h3 class="jobSectionHeader">
Looking for more than just high-volume blood draws?</h3>

If you're an experienced phlebotomist or lab technician who takes pride in precision, patient care, and doing things the right way&mdash;not just the fast way&mdash;clinical research may be the next step in your career.

At Peninsula Research Associates, our lab professionals work in a structured, calm, and purpose-driven environment, supporting clinical trials that help advance new treatments for allergy and immunology-related conditions. 


<h2 class="jobSectionHeader">Why Lab Professionals Choose Clinical Research</h2>
<ul>
<li>Predictable weekday schedule (no nights, no weekends, no emergency draws)
</li>
<li>More time and control during patient visits and specimen handling
</li>
<li>Specialized lab work beyond routine phlebotomy (processing, PK handling, shipping)
</li>
<li>Smaller, collaborative teams where your role is respected
</li>
<li>Meaningful purpose&mdash;your work directly supports future medical treatments
</li>
<li>Clear growth pathway into higher-paying clinical research roles
</li>
</ul>This role is ideal for lab professionals who value accuracy, organization, and consistency, and who want to grow their skills beyond traditional lab or hospital settings. 


<h2 class="jobSectionHeader">Career Growth Opportunity</h2>

PRA strongly supports internal growth. High-performing Laboratory Technicians / Phlebotomists have the opportunity to progress into a Clinical Research Coordinator (CRC) role, which offers:
<ul>
<li>Increased responsibility
</li>
<li>Broader study ownership
</li>
<li>Higher compensation
</li>
<li>Long-term career growth within clinical research
</li>
</ul>If you're curious about research and want a role that can evolve with you, this position offers a clear entry point. 


<h2 class="jobSectionHeader">Position Details</h2>
<ul>
<li>Position Type: Full-time
</li>
<li>Schedule: Monday&ndash;Friday, 8:00am&ndash;5:00pm
</li>
<li>Location: Onsite in Rolling Hills Estates, CA (no remote or hybrid)</li></ul> 

<h2 class="jobSectionHeader">The Role</h2>

The Laboratory Technician / Phlebotomist is a key member of the clinical research team, supporting studies through specimen collection, processing, documentation, and shipment in compliance with Good Clinical Practice (GCP), study protocols, and safety regulations.

You'll work in a controlled clinical research environment with scheduled visits, detailed protocols, and strong operational support, allowing you to focus on quality and precision. 


<h2 class="jobSectionHeader">Who Thrives in This Role</h2>
<ul>
<li>Lab professionals who value precision over speed
</li>
<li>Phlebotomists looking for predictability and balance
</li>
<li>Candidates curious about clinical research and career growth
</li>
<li>Team players who take pride in quality, compliance, and patient experience
</li>
</ul>Responsibilities:
<ul>
<li>Laboratory and Clinical Procedures
<ul><li>Perform phlebotomy, urine collection, and sample processing (centrifuging, aliquoting, labeling).</li>
<li>Prepare lab kits for each subject based on study protocols.</li>
<li>Ship biological specimens following IATA guidelines and protocol requirements.</li>
<li>Maintain specimen logs, shipping records, temperature logs, and other documentation.</li>
<li>Conduct point-of-care tests (e.g., urine drug screens, pregnancy tests).</li>
<li>Assist with patient procedures including vital signs, ECGs, and physical/neurological exam setups.</li>
<li>Clean and sanitize lab equipment and work areas daily.</li>
<li>Perform and document equipment calibration and ensure safety compliance (OSHA, HIPAA).</li>
</ul></li><li>Data and Documentation
<ul><li>Accurately record lab results and maintain electronic and paper logs in systems such as CRIO or eCRFs.</li>
<li>Respond to and resolve electronic data queries.</li>
<li>Verify accuracy and completeness of data entries and study documentation.</li>
<li>Participate in quality control and assurance initiatives to ensure regulatory compliance.</li>
</ul></li><li>Operational Support
<ul><li>Monitor and maintain inventory of lab kits and supplies.</li>
<li>Order dry ice and other lab necessities.</li>
<li>Destroy expired kits and log per protocol.</li>
<li>Support preparation of study-specific training materials and lab manuals.</li>
<li>Collaborate with study coordinators and medical staff to meet visit protocol requirements.</li>
<li>May assist with infusion monitoring under clinician supervision.</li>
</ul>
</li></ul>Requirements:
<ul>
<li>Must be certified in phlebotomy</li>
<li>Must have at least one full year of experience performing phlebotomy multiple times daily</li>
<li>Previous experience in clinical research is a huge plus</li>
<li>Proficient with Microsoft Office (Excel, Outlook, Word) and database systems.</li>
<li>Must be comfortable with performing Research Assistant tasks</li>
<li>Ability to handle potentially hazardous materials safely.</li>
<li>Strong organizational, time management, and multitasking skills.</li>
<li>Excellent verbal and written communication; strong interpersonal skills.</li>
<li>Ability to work independently and as part of a cross-functional team.</li>
<li>Customer-service mindset and high level of professionalism.</li></ul></div>

Laboratory Technician/Phlebotomist

Flourish Research

<div>Flourish Research is looking for motivated, talented, creative individuals who want to learn and grow in their careers while contributing to research that changes lives! We offer an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities. 
 
We are actively hiring a Patient Care &amp; Front Desk Coordinator at the Murrieta site location. This site is part of our Greater Los Angeles oncology research network and was formerly operated as Valkyrie Clinical Trials. We are proud to welcome the Valkyrie team into the Flourish Research network. 
 
The Patient Care &amp; Front Desk Coordinator is an essential member of our team. They ensure smooth administrative operations while providing an impeccable patient experience in every interaction. This individual is responsible for creating a welcoming, positive, and supportive environment for patients and study participants. They are the gatekeepers, setting the example of what patients can expect during their care journey at Flourish Research. 
 
Shift: Monday-Friday, 8:30 AM - 5 PM (occasional weekends) 
Location: 2080 Century Pk E, Suite 803, Los Angeles, CA 90067 
Compensation: $20/hr - $25/hr, depending on experience 
Benefits: Health, dental, and vision insurance plans, 401(k) with 4% match, tuition reimbursement, parental leave, referral program, employee assistance program, life insurance, disability insurance, and 15 days of PTO + 10 company holidays.
RESPONSIBILITIES<ul><li>
Support site leadership and members of the research team by working on various projects as requested and assigned</li><li>
Manage front desk operations, including greeting, check-in, and coordination of patients, study participants, and visitors</li><li>
Answer phones and manage clinic appointment scheduling, including routing calls and handling high-volume communication with patients, staff, and vendors</li><li>
Coordinate, schedule, and follow up on patient appointments while monitoring provider schedules and clinic calendars</li><li>
Prepare, maintain, and verify patient charts, registration, and documentation for accuracy and completeness</li><li>
Guide patients through intake processes, ensuring all required documentation is collected and complete</li><li>
Serve as a liaison between patients, physicians, study coordinators, and internal teams to ensure seamless communication</li><li>
Assist with clinic flow to support timely patient throughput and resolve scheduling or operational issues</li><li>
Perform documentation and data entry within EMR and internal systems</li><li>
Ensure exam rooms are ready, stocked, and organized throughout the day</li><li>
Request and manage medical records and related documentation</li><li>
Communicate effectively with internal teams, imaging centers, billing, administration, and external partners</li><li>
Support monitor visit logistics, including scheduling, check-ins, and room assignments</li><li>
Order, track, and manage site supplies, snacks, and general inventory</li><li>
Sort and distribute mail, manage faxes, and maintain organized clinical and regulatory files</li><li>
Manage invoices, receipts, and patient reimbursements</li><li>
Schedule maintenance and assist with basic procurement needs</li><li>
Assist in event planning and coordination</li><li>
Perform occasional local pickups or deliveries as needed</li><li>
Ensure compliance with HIPAA, GCP, IRB, and company policies and procedures</li><li>
Maintain patient confidentiality and uphold professionalism in all interactions</li><li>
Assist with training new staff as needed</li><li>
Other clerical and administrative duties as assigned</li></ul>
QUALIFICATIONS<ul><li>
Minimum education requirement of a High School Diploma or an Associate's Degree</li><li>
1&ndash;3+ years of administrative support experience, preferably in a medical or clinical setting</li><li>
Medical office administrative experience is preferred</li><li>
Medical assisting experience is a plus</li><li>
Experience in a high-volume, patient-facing healthcare environment strongly preferred</li><li>
Ability to manage high-volume calls, scheduling, and follow-up communications</li><li>
Strong attention to detail with the ability to maintain accurate records and documentation</li><li>
Excellent interpersonal, customer service, and communication skills (written and oral)</li><li>
Ability to collaborate with internal teams and external stakeholders</li><li>
Demonstrates professionalism, integrity, and accountability</li><li>
Strong decision-making skills and ability to handle sensitive situations with discretion</li><li>
Ability to prioritize, multitask, and adapt in a fast-paced, changing environment</li><li>
Proficiency with Microsoft Office (Office365) and general computer systems</li><li>
Ability to work both independently and as part of a team</li><li>
Maintains confidentiality and aligns with company policies and core values</li></ul>
Flourish Research offers an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities. Apply today to learn more about how you can join us in our mission to save and improve the lives of others! 
 
Flourish Research is where clinical trials thrive. 
 
Flourish Research represents one of the industry's most progressive and diversified clinical trial companies with robust capabilities in the therapeutic areas of oncology cardiology/metabolic disorders/renal, CNS, pulmonology, and vaccines. 
 
At Flourish Research, we strive toward excellence. In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of their race, color, gender identity, religion, ethnicity, physical abilities, age, sexual orientation, or veteran status. We embrace employees, customers, and patients from these underrepresented groups to help make this vision a reality. 
 
Flourish Research is driven by a diverse and inclusive community of passionate people who are committed to improving the quality of life of communities around the world. Flourish is committed to a safe work environment where all employees, customers, and patients are included, and treated with dignity and respect. 
 
Flourish Research strives to build an organization that attracts and leverages diversity in our staff, which reflects the diversity of our local communities. We promote education, acceptance, and inclusion because there is beauty in diversity. The more diversity we have in our team, the more unique perspectives, and ideas we share, and the better prepared we are to serve our communities. WE SEE YOU. WE ARE YOU. WE EMBRACE YOU. WE CELEBRATE YOU! 
 
Flourish Research is an equal employment opportunity employer. Employment decisions are based on merit and business needs, and not on race, color, sex, (including pregnancy and gender identity), citizenship status, national origin, ancestry, gender, sexual orientation, age, religion, creed, physical or mental disability, genetic information, marital status, veteran status, political affiliation, or any other factor protected by law. Flourish Research complies with the law regarding reasonable accommodation for handicapped and disabled employees. 

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Patient Care Coordinator / Front Desk (Clinical Research)

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