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senior data analyst

clinical data manager digital medicine and translational imaging fsp east coast us

Parexel

<div>Job Summary:
We are looking for a self-directed professional to support clinical data management efforts for the biomeasures endpoints projects. This individual will be responsible for acquiring, processing, and reviewing patient data and records, organizing clinical data forms, implementing data management plans including data preparation and validation activities and define ways to improve operational processes for these activities. They will act independently and in collaboration with study teams seeking to develop and validate novel digital endpoints across different therapeutic areas.
In close partnership with colleagues from Research teams from Research and Development, They will play a key role in the deployment of novel digital endpoints into clinical studies, collection, management and analysis of sensor data, both in patients and healthy volunteers. This role will be central to the deployment and scaling of digital solutions into clinical trials where these technologies may be utilized as efficacy endpoints and provide value to key stakeholders including patients, physicians, payers.
Key Responsibilities:<ul><li>
Data Management POC for studies in which we are included in</li><li>
Responsible for mapping local study dictionaries to CDISC Standards</li><li>
Participate and contribute to the development of operational plans to ensure data quality and completeness</li><li>
Develop, Implement, and Conduct data quality checks as needed for work/studies</li><li>
Work closely with the various stakeholders to understand evolving project portfolio needs, and integration into the systems and requirements; supporting studies with a wide range of disease domains</li><li>
Contribute technical expertise toward the design, implementation, and scaling up of sensor systems and analytics</li><li>
As a medical informaticist, ensure collection, organization, curation, storage and safeguarding of patient data from lab, asset teams, and external collaboration studies is consistent with 21CFR part 11</li><li>
Contribute to the overall architecture of the existing data pipelines and workflows, recommends and implements improvements</li><li>
Track emerging study data and works closely with data science team to ensure the effectiveness of tools and data quality</li><li>
Manage own time to meet agreed targets</li><li>
Work under general supervision. Performs assignments using established procedures and general instruction</li><li>
Share learnings with key stakeholders and the scientific community through presentations and peer-reviewed publications.</li></ul>
Minimum Requirements:<ul><li>
Master's degree in Health Informatics, Computer Science, Information Systems, or similar field required</li><li>
A minimum of 5+ years of technical experience required, including:</li><li>
Python</li><li>
Unix/Linux environments</li><li>
Version control systems (ex. Git)</li><li>
AWS or other cloud-based development</li><li>
Electronic data captures (EDC) solutions, e.g., REDCap, Encapsia, Oracle Clinical, Medidata Rave</li><li>
Familiarity with pharmaceutical informatics standards like CDISC and MedDRA</li><li>
GCP experience</li><li>
Strong interpersonal and collaboration skills</li><li>
Demonstrate the ability to build consensus and be agile to changing circumstances and priorities</li><li>
Hands-on experience with Clinical Data Management, including Case Report Form (CRF) design, CRF annotation, database design, data collection, data-entry, data validation, discrepancy management, medical coding, data extraction, database locking, and regulatory requirements</li></ul>
#LI-CF1 
#LI-REMOTE</div>

Clinical Data Manager, Digital Medicine and Translational Imaging - FSP - East Coast US

GoHealth Urgent Care

<div>It's fun to work in a company where people truly BELIEVE in what they are doing!
We're committed to bringing passion and customer focus to the business.
Physician Opportunity &ndash; Mercy-GoHealth Urgent Care - St. Louis Region 
 We&rsquo;re excited to offer a highly competitive sign-on bonus of $25,000 for physician roles 
Mercy-GoHealth Urgent Care is seeking a dedicated and compassionate Physician to join our team in St. Louis, Missouri. We offer flexible scheduling options, including full-time and part-time roles, in a collaborative and modern clinical environment.
What You Can Expect<ul><li>
Competitive compensation package with a generous sign-on bonus</li><li>
Monthly volume bonus based on patient metrics</li><li>
Quarterly bonus (up to 5% of base salary) tied to patient satisfaction and quality outcomes</li><li>
Comprehensive benefits starting day one: health, dental, vision, CME allowance and more!</li><li>
Retirement plans with employer contributions and matching</li><li>
Relocation assistance (if applicable) and professional liability coverage</li><li>
Eligibility for Public Service Loan Forgiveness (PSLF)</li><li>
Beautiful, state-of-the-art centers equipped with imaging, labs, and Epic EMR</li><li>
Supportive staffing model including radiologic technologists, experienced medical assistants, and advanced practitioners</li><li>
Part of one of the fastest-growing urgent care networks in the country</li></ul>
What We&rsquo;re Looking For<ul><li>
Board-certified or board-eligible in Family Medicine, Emergency Medicine, or Med/Peds</li><li>
Active state medical license</li><li>
2&ndash;5 years of post-residency clinical experience, with at least 18 months in an urgent care or emergency medicine setting</li><li>
Experience treating patients across all age groups</li><li>
Proficiency in minor procedures such as suturing and splinting, and in reading EKGs and X-rays</li><li>
Strong communication and listening skills</li><li>
Comfort collaborating with advanced practice providers</li></ul>
Your Role
As a Physician at Mercy-GoHealth, you&rsquo;ll independently provide a wide range of clinical services, including:<ul><li>
Examining and treating patients with acute conditions</li><li>
Taking medical histories and ordering diagnostic tests</li><li>
Making diagnoses and prescribing medications</li><li>
Performing minor procedures and administering vaccinations</li><li>
Documenting patient progress and coordinating follow-up care</li><li>
Supervising and collaborating with PA/NPs, including remote supervision and credentialing support</li><li>
Working 8- or 12-hour shifts in a fast-paced, patient-focused setting</li></ul>
This role offers the opportunity to deliver high-quality care in a modern, integrated healthcare environment, with room for professional growth and development.
Interested in learning more or scheduling a tour? Let&rsquo;s connect.
We&rsquo;re excited to meet physicians who are passionate about making a difference in urgent care.
Contact:
Soheyl Daudi, Provider Recruiter
soheyl.daudi@Gohealthuc.com
Take a Virtual Tour of GoHealth Urgent Care<ul><li>YouTube</li></ul>
Enjoy the videos and music you love, upload original content, and share it all with friends, family, and the world on YouTube. 
Set up email alerts as new job postings become available that meet your interest!
If you like wild growth and working with happy, enthusiastic over-achievers, you'll enjoy your career with us!</div>

Urgent Care Physician - Full Time - St. Louis

Lifebit

<div>A World-Changing Company at Lifebit

At Lifebit, we're driven by the mission to make complex data analysis simpler and more accessible. We empower key institutions worldwide to revolutionize their data utilization and technology integration. Lifebit is powering the world&rsquo;s federated data platforms for population-scale health and life sciences. Our Federated AI Platform is trusted across federal health agencies, national health systems, and global pharma to unlock sensitive biomedical and real-world data securely, compliantly, and at scale.

We are rapidly expanding our presence in the U.S. federal health market and building a local team to support programs across the various federal agencies. Join us if you're inspired to tackle meaningful challenges and want to launch your career in health technology and cloud-based data solutions. 
The Role

This is an exciting opportunity to join Lifebit&rsquo;s growing US team. This is a hybrid technical and customer-facing role, bridging sales, solution engineering, and customer success. We are looking for a Solutions Manager with experience in one or more of the following specialties: Bioinformatics/Computational Biology, Cloud Infrastructure, Real-World Data and/or Genomic Medicine. The ideal candidate understands real-world data (RWD), harmonization, and privacy-preserving linkage &mdash; and can translate complex technical capabilities into value for federal stakeholders and researchers. In addition, you enjoy working hands-on with Lifebits commercial team, scientists, software engineers, and clients to solve challenges in the world of Genomics and Precision Medicine. 
You will support federal business development efforts with technical credibility in meetings, demos, and proposals. Acting as the technical solutions lead for prospective and current customers (e.g., DHA, NIH/NIA, CMS-linked studies) you will ensure customer success post-sale by guiding deployment, adoption, and integration of Lifebit&rsquo;s Federated AI Platform. 
Based in the Washington, DC/DMV area, you&rsquo;ll work closely with prospective and current clients, showcasing the capabilities of Lifebit&rsquo;s platform through tailored demonstrations and technical selling. This position is integral to enabling customer success by aligning Lifebit&rsquo;s solutions with clients&rsquo; technical needs and business goals. 
Your Role and Responsibilities

Pre-Sales &amp; Federal Engagement
<ul>
<li>Partner with Sales and Federal Programs leadership to position Lifebit&rsquo;s platform in capture and proposal activities.</li>
<li>Deliver technical presentations, demos, and solution workshops to Canadian health agencies.</li>
<li>Translate RFI/RFP requirements into clear solution architectures aligned to Lifebit&rsquo;s product capabilities.</li></ul> 


Solution Delivery &amp; Customer Success
<ul>
<li>Serve as the technical point of contact for customers post-sale, ensuring seamless onboarding and adoption.</li>
<li>Guide deployments around data ingestion, harmonization (OMOP, HL7 FHIR, CDISC), and Privacy-Preserving Record Linkage (PPRL).</li>
<li>Work with customer admins and researchers to configure federated access, metadata cataloging, and TRE (Trusted Research Environment) capabilities.</li>
<li>Experience in working with a variety of data sources from Claims, third-party EHR and CMS.</li></ul> 


Collaboration &amp; Enablement
<ul>
<li>Act as a bridge between customers, sales, and product engineering &mdash; feeding back federal-specific requirements.</li>
<li>Train and enable end-users (researchers, analysts, clinicians) across no-code, low-code, and high-code personas.</li>
<li>Contribute technical expertise to proposals, whitepapers, and federal solution documents.</li></ul> 


What You Bring to the Table
<ul>
<li>Education: MSc in Biology, Bioinformatics, Computational Biology, or a closely related advanced technical field.</li>
<li>3&ndash;5+ years in a technical solutions, solutions engineering, or customer success role (ideally in federal health / life sciences).</li>
<li>Strong understanding of real-world data (RWD): claims, EHR, genomics, imaging, unstructured data.</li>
<li>Experience with data harmonization and interoperability standards (OMOP, HL7 FHIR, CDISC, Sentinel CDM).</li>
<li>Experience with scripting or analytical tools (Python, SQL, RStudio, or Jupyter) and workflow language (Nextflow, Snakemake or WDL)</li>
<li>Familiarity with federated architectures and PPRL/linkage technologies (e.g., Datavant).</li>
<li>Comfort engaging with both technical and non-technical stakeholders in NIH, DHA, or comparable agencies.</li>
<li>Strong presentation, communication, and proposal support skills.</li></ul> 


Preferred Qualifications
<ul>
<li>Experience supporting Federal health RFPs, proposals, or capture efforts.</li>
<li>Knowledge of FedRAMP, HIPAA, NIST 800-53, FISMA Moderate requirements.</li>
<li>Hands-on with research/analytics tools (RStudio, Jupyter, SQL, Python) and cloud (AWS GovCloud / Azure Government).</li>
<li>Background in biomedical informatics, data engineering, or public health research.</li></ul> 


What We Offer

Lifebit is synonymous with a dynamic work culture that encourages both personal and professional growth. Our mission-driven organization is dedicated to making a significant impact in science and healthcare.

We provide a comprehensive benefits package, including:
<ul>
<li>Compensation: Your work is rewarded with a competitive salary and performance-based incentives.</li>
<li>Professional Development: You are granted an annual personal development budget and access to leading industry conferences, training, and certifications.</li>
<li>Flexible Working: Receive 25 days of annual leave and hybrid remote work to maintain a healthy work-life balance.</li>
<li>Diverse Team Culture: Join an international and diverse team passionate about transforming healthcare through data.</li>
<li>Deep Technology &amp; Science: Get exposure to problems and applications in the cloud, data analysis, ML, life sciences, and big data fields</li>
</ul>
Join us at Lifebit for a career that promises to be your next significant venture, dedicated to advancing the scientific and healthcare fields by delivering transformative platforms for aging, defense health, and biomedical research. Don't miss the chance to be part of our mission! 
Life at Lifebit

Lifebit is dedicated to fostering an environment where employees can flourish, valuing individual strengths, skills, and passions. We prioritize health and well-being, offering comprehensive benefits and support. Our hybrid work model encourages in-office collaboration to maximize creativity and innovation, with flexibility for remote work as needed. Lifebit is proud to be an equal opportunity employer, committed to diversity, equity, and inclusion. 
Join us in reshaping the future of data analysis and technology integration. 
Location: Washington DC</div>

Senior Solutions Manager - Federal Health - USA

<div>Join our dynamic Patient Safety team as a Senior Physician where you'll leverage your medical expertise to ensure the safety of patients in clinical trials and post-marketing settings. In this pivotal role, you'll perform comprehensive medical reviews, provide expert safety monitoring, and deliver pharmacovigilance guidance across assigned projects. You'll also mentor junior team members while tackling complex safety evaluations that directly impact patient wellbeing and regulatory compliance.<h2 class="jobSectionHeader">
About the Role</h2>
As a Senior Physician in Patient Safety, you'll serve as the medical authority on safety profiles for assigned products, ensuring compliance with global regulations while providing critical medical insights. You'll collaborate with cross-functional teams, interact with clients, and contribute to the continuous improvement of our pharmacovigilance processes.
Key Accountabilities:
General<ul><li>
Maintaining a good working knowledge of the Adverse event/Safety profile of assigned products, labeling documents, data handling conventions, client&rsquo;s guidelines and procedures, and global drug safety regulations and guidelines</li><li>
Maintaining an awareness of global regulatory requirements, reporting obligations and organizing workload to ensure compliance with internal and regulatory timelines for adverse event reporting</li><li>
Communicating and discussing issues related to review process with Line Manager/ Project Leader/Designee</li><li>
Interacting with internal and external stakeholders for resolving issues</li><li>
Attending and/ or presenting at client/cross functional meetings along with other stakeholders. Working as Subject Matter Experts (SMEs)</li><li>
Assisting the Project Lead/Functional Lead for audits and inspections</li><li>
Provides inputs for process improvements</li><li>
Works closely with Project Lead/Functional Lead for process co-ordination and to ensure meeting all Key Performance Indicators (KPIs) for the process</li><li>
Function as pharmacovigilance representative/safety scientist</li><li>
Attend/support Bid defense meetings</li><li>
Actively mentoring Patient Safety Physicians to develop their skills and expertise</li></ul>
Case report medical review (as applicable)<ul><li>
Performing medical review of cases not limited to (including complex and challenging cases requiring expert judgement)), clinical trial, and literature cases including combination products {drug-device}) according to client/Parexel Standard Operating Procedures (SOPs; as applicable) and liaising with the client, as require</li></ul><ul><li>
Writing Pharmacovigilance/Marketing Authorization Holder (MAH) comment and assessing company causality</li><li>
Review appropriateness of medical content in narrative for medical coherence</li><li>
Assessing seriousness, listedness / expectedness of reported events.</li><li>
Providing medical inputs to case processing team</li></ul><ul><li>
Raising appropriate follow-up queries for relevant information from the reporter/HCP (Health Care Professional)</li><li>
Review and verify appropriate selection of adverse events from source documents, assign appropriate Medical Dictionary for Regulatory Activities (MedDRA) code, review narrative</li><li>
Identify and resolve case issues, coordinate with client therapeutic/legal team</li><li>
Provide guidance to junior physicians on case assessment methodologies</li></ul>
Periodic reports (as applicable)<ul><li>
Reviewing and/ or authoring of aggregate reports for medical content and consistency in accordance with client requirements and SOPs</li></ul><ul><li>
Providing medical inputs into, and supporting the preparation of key regulatory documents including but not limited to, Periodic Benefit-Risk Evaluation Reports (PBRERs)/ Periodic Safety Update Reports (PSURs), Signal Evaluation Reports (SERs), Health Authority (HA) response documents, Development Safety Update Reports (DSURs), Clinical Overviews (COs), Addendum to Clinical Overview (ACOs), Health Hazard Evaluation reports (HHEs), etc.</li><li>
Clinical Expert Statements and other documents as required</li><li>
Review reports assessed by junior team members for accuracy and completeness</li></ul>
Medical monitoring (as applicable)<ul><li>
Answering day to day medical and scientific questions, provide daily medical support to Parexel staff or site (investigator/study coordinator), as needed</li><li>
Review and sign off adverse events report for accuracy and clinical importance, relationship to the study drug as well as for severity and seriousness; provide sponsors with periodic experience reports summarizing adverse events as required by the sponsor or authorities</li><li>
Attend and present material (such as therapeutic area training), as requested, at internal and external meetings (such as investigator meetings)</li><li>
Provide medical safety expertise to client per request</li><li>
Review and sign off Data Management line listings (including adverse events, laboratory data, vital signs data, medical history, physical examination, concomitant medication, efficacy end points), establish the presence or absence of clinically meaningful trends and, if noted, follow up as appropriate with the project team, sponsor, investigator, and Regulatory Authorities</li><li>
Review and sign off technical documents written by Parexel with respect to medically relevant matters with particular attention to those relating to patient safety</li><li>
Review coding of adverse events, medical history and concomitant medications for accuracy and consistency</li><li>
Review of patient profile report as needed</li><li>
Provide support for the preparation of clinical protocols, integrated clinical and statistical summary reports, journal articles, and other documents for clients/sponsors in conjunction with clients/sponsors or in conjunction with other Parexel departments</li><li>
Attend and present material as requested, at internal and external meetings (e.g., investigator meetings, therapeutic area training, Regulatory Authority meetings)</li></ul>
Literature review (as applicable)<ul><li>
Review of literature for product safety assessment and potential safety issues</li><li>
Expert in reviewing literature references including triaging, summarizing and providing MAH comments for aggregate reports and for various signal management activities</li></ul>
CSR Narratives (as applicable)<ul><li>
Performing medical review of Clinical study report narratives according to the client&rsquo;s guidelines and SOPs</li></ul>
Provide medical guidance to PV team/study team<ul><li>
Provide medical guidance to safety staff during the case processing cycle</li><li>
Provide input as necessary to Feasibility Studies, Data Monitoring Committees (DMCs), Clinical Endpoint Committees (CECs)</li><li>
Provide medical input into Pharmacovigilance workflows and projects as required</li><li>
On an as-needed basis, provide support in mentoring or training of new hired physicians</li></ul>
Signal Detection and Management (as applicable)<ul><li>
Perform signal detection activities in accordance with client conventions/SOPs and within pre-decided timeframes. Perform medical assessment of safety alerts obtained from data mining activities</li><li>
Perform signal validation activities</li><li>
Author/review SERs. Perform case analysis, review literature summaries, check draft for medical and scientific accuracy and cohesiveness</li><li>
Author/review responses to HA requests and other safety documents</li><li>
Providing oversight and relevant inputs to Medical Writers (MWs) authoring SERs, Signal validations etc.</li><li>
Managing safety signals on project specific tools (e.g., Signal Tracking System, Signal management tools, etc.)</li><li>
Contribution to Safety Management Team (SMT) meetings: Data analysis/ review, content creation, presentation/ facilitation, drafting of meeting minutes</li><li>
Training and mentoring junior team members on signal detection methodologies</li></ul>
Brand safety Physicians (as applicable)<ul><li>
Contribute to Pharmacovigilance and Risk Management planning for designated products by preparation of safety surveillance strategy, and highlighting and tracking potential issues</li><li>
Support the preparation and maintenance of Risk Management Plans</li><li>
Prepare and review periodic safety reports (PBRER/PSUR, DSUR, European union renewal, HHE and other Annual Safety/addendum reports) in accordance with regulatory requirements and SOPs</li><li>
Support the preparation and maintenance of safety sections of the Company Core Data Sheet, local labels and Development Core Safety Information (DSCI)</li><li>
Coordinate safety activities between Drug Safety Unit/team and internal and external partners</li><li>
Conduct/support signal detection and evaluation according to SOPs and guidelines</li><li>
Prepare safety assessments, SERs, as necessary, for potential signals or issues (product quality)</li><li>
Perform review and summarization of literature citations including epidemiology background research</li><li>
Provide safety content review of clinical protocols, study reports, Investigators Brochures, and other related documents</li><li>
Contribute to regulatory agency submissions (Investigational new drug applications, new drug applications, Marketing authorization applications, Variations and Renewals) by reviewing safety data and preparing relevant sections of the filing documents and submission packages</li><li>
Participate in or provide input for Drug Safety Monitoring Boards or independent monitoring committee meetings, as applicable</li></ul>
Therapeutic Area Expert (as applicable)<ul><li>
Serve as a subject matter expert within the designated Therapeutic Area, providing specialized knowledge to support drug safety initiatives and decision-making processes</li><li>
Collaborate with the TA Lead to implement strategic plans and enhance the overall expertise within the Therapeutic Area</li><li>
Contribute to the development and delivery of targeted training programs, elevating the knowledge base of fellow physicians and cross-functional teams</li><li>
Actively participate in internal and external scientific forums, representing Parexel's medical expertise through presentations, publications, and thought leadership activities</li><li>
Apply deep therapeutic knowledge to optimize pharmacovigilance processes, ensuring best practices are followed and continuously improved</li><li>
Mentor junior physicians within the TA, fostering their professional growth and encouraging their contributions to the field</li><li>
Support the TA Lead in identifying emerging trends and potential opportunities for innovation within the Therapeutic Area</li><li>
Engage in cross-functional projects, offering expert guidance to enhance the quality and efficiency of drug safety assessments</li></ul>
Skills:<ul><li>
Experience in clinical medicine (general or specialist qualifications) which is expected to be kept up to date</li><li>
Demonstrated success in technical proficiency and scientific creativity</li><li>
Ability to work on complex tasks requiring in-depth evaluation</li><li>
Good knowledge of drug safety and the drug development process</li><li>
Ability to exercise judgment within broadly defined practices and policies</li><li>
Good presentation and verbal/written communication skills</li><li>
Good interpersonal skills</li><li>
Client focused approach to work</li><li>
Computer proficiency, an ability to work with web-based applications and familiarity with the Windows operating system and Microsoft Office apps</li><li>
An ability to comprehend various regulatory or client requests and be able to strategize a handling approach</li><li>
Experience mentoring junior team members</li><li>
A flexible attitude with respect to work assignments and new learnings</li><li>
An ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail</li><li>
An ability to assess the clinical relevance of medical data and to interpret its clinical meaning is essential</li><li>
A willingness to work in a matrix environment and to value the importance of teamwork</li><li>
Strong knowledge of international drug regulation including ICH GCP, GVP, and all other applicable regulations and guidelines</li></ul>
Knowledge and Experience:<ul><li>
US Board Certification/board eligibility or regional equivalent for Canada</li><li>
3 - 5 years previous experience in pharmacovigilance and/or medical monitoring is required.</li><li>
Previous CRO experience is highly desirable, but individuals with relevant experience as a Patient Safety/Drug Safety Physician within Industry will also be considered.</li><li>
Good knowledge/understanding of medical terminology</li><li>
Relevant experience in pharmacovigilance/ Drug Safety/ Clinical Practice</li></ul>
Education:<ul><li>
Bachelor of Medicine, Bachelor of Surgery (MBBS) / Doctor of Medicine (MD)/ Medically qualified from an acknowledged Medical School</li><li>
Completion of at least basic training in clinical medicine (residency, internship etc.)</li></ul>
This role offers the flexibility to work from home in either the US or Canada.
#LI-KS1 
#LI-REMOTE</div>

Senior Physician, Patient Safety (Senior Drug Safety Physician)

CloseKnit

<div>Certified Medical Assistant (Full-Time) / Washington, DC (In-Person)
Employer: CloseKnit
Job Type: Full-Time | FLSA Status: Non-Exempt
Work Setting: In-Person Clinical Environment
About CloseKnit
CloseKnit is a growing, patient-centered healthcare organization dedicated to delivering high-quality, accessible primary and immediate care. We pride ourselves on fostering a dynamic and organized work environment where administrative excellence meets clinical expertise. Our teams value collaboration, innovation, integrity, and accountability, and we strive to deliver seamless patient experiences and operational efficiency across all clinical settings.
Join a supportive, inclusive workplace that encourages professional growth and continuous learning while maintaining a commitment to compassionate care and exceptional patient outcomes.
Position Summary
The Medical Assistant plays a pivotal role in supporting clinicians and ensuring efficient daily operations. This position requires full-time availability and may include some weekend shifts as needed. Work hours may vary based on location, patient volume, and business needs.
Medical Assistants at CloseKnit perform a blend of clinical and administrative duties, working closely with providers and staff to deliver accurate, timely, and high-quality patient care.
Work Schedule &amp; Location Flexibility<ul><li>
Work schedules may vary depending on practice location, patient demand, and operational requirements.</li><li>
Based on business needs, Medical Assistants may be required to work at multiple clinical locations.</li><li>
Flexibility is essential to support coverage needs and ensure continuity of patient care across practices.</li><li>
Work hours may include evenings, weekends, and occasional holidays based on patient needs.</li></ul>
Core Responsibilities
Clinical Responsibilities<ul><li>
Assist providers with exams, diagnostic testing, and in-office procedures.</li><li>
Conduct clinical intake, including detailed patient histories and vitals.</li><li>
Administer injections and medications as directed by licensed providers.</li><li>
Perform venipuncture and collect lab specimens (blood, urine, POC testing, etc.).</li><li>
Operate medical equipment such as EKG machines and other diagnostic tools.</li><li>
Prepare specimens for laboratory testing and conduct basic lab procedures.</li><li>
Educate patients on treatment plans, follow-up care, and self-care instructions.</li><li>
Maintain clean, stocked, and properly sanitized exam rooms.</li><li>
Support quality initiatives, including PCMH-related tasks and clinical KPI adherence.</li></ul>
Administrative Responsibilities<ul><li>
Greet and register patients with a professional, friendly demeanor.</li><li>
Manage check-ins, check-outs, and verify insurance coverage.</li><li>
Maintain and update patient information in the electronic health record (EHR).</li><li>
Schedule and reschedule patient appointments, including physicals and chronic care visits.</li><li>
Process prior authorizations, referrals, and daily patient callbacks.</li><li>
Track and link diagnostic imaging orders to results.</li><li>
Manage inventory, medical supplies, and perform daily opening and closing procedures.</li><li>
Ensure compliance with all regulatory requirements, including HIPAA and OSHA.</li><li>
Support staff coverage needs and assist team members when necessary.</li><li>
Communicate clearly and professionally, both orally and in writing.</li></ul>
Technical &amp; Operational Expertise<ul><li>
Proficiency in EHR systems and medical software.</li><li>
Ability to troubleshoot minor equipment or software issues.</li><li>
Stay current with evolving clinical practices and technologies.</li><li>
Provide basic technical guidance to team members regarding medical equipment or EHR workflows.</li></ul>
Professional Expectations<ul><li>
Maintain patient confidentiality and uphold ethical and legal standards.</li><li>
Demonstrate professionalism through punctuality, appropriate attire, and respectful communication.</li><li>
Exhibit strong problem-solving skills and adaptability in a fast-paced environment.</li><li>
Deliver patient-centered service with empathy, patience, and compassion.</li></ul>
Required Qualifications<ul><li>
High School Diploma or GED.</li><li>
Completion of an accredited Medical Assistant training program.</li><li>
Current CCMA, CMA, or RMA certification.</li><li>
Current BLS or CPR certification.</li><li>
2+ years of Medical Assistant experience.</li><li>
Experience using EMR systems.</li></ul>
Competency in:<ul><li>
Clinical intake and patient data collection.</li><li>
Lab specimen collection (including venipuncture).</li><li>
Point-of-care testing.</li><li>
EKG testing.</li><li>
Must meet all applicable state requirements and maintain active certifications.</li></ul>
Preferred Qualifications<ul><li>
2+ years of customer service experience.</li><li>
Experience in primary care, internal medicine, immediate care, or emergency care.</li><li>
Familiarity with systems such as eClinicalWorks or Athena.</li><li>
Proficiency in Microsoft Office Suite.</li><li>
Knowledge of population health initiatives.</li><li>
Understanding HIPAA, OSHA, and other regulatory standards.</li></ul>
Physical Requirements
Requires the ability to stand and sit for hours at a time (with some bending and stooping), ability to use manual dexterity in relation to clinical requirements, and ability to lift 50 lbs.
Reasonable accommodations available for qualified individuals.
Working Relationships<ul><li>
Clinicians (providers and advanced practice clinicians).</li><li>
Clinical support staff.</li><li>
Administrative and practice leadership teams.</li></ul>
Why Join CloseKnit<ul><li>
Competitive compensation based on experience and qualifications.</li><li>
Health, dental, and vision insurance.</li><li>
Life insurance.</li><li>
401(k) retirement plan.</li><li>
Paid time off (vacation, holidays, sick leave).</li><li>
Professional development and continuing education opportunities.</li><li>
Supportive, collaborative, and inclusive work culture.</li></ul>
To advance your application, you must email your current (not expired) CCMA, CMA, or RMA certification to amanda.duncan@closeknit.com. Once received, you will be contacted to schedule a phone interview. Thank you!</div>

Certified Medical Assistant (Full-Time) / Washington, DC (In-Person)

Johns Hopkins Health System

<div></div><div><div><div>Requisition #:</div><div>
664824</div>
<div>Location:</div><div>
Sibley Memorial Hospital, Washington, DC 20016
</div><div>Category:</div><div>
Nursing Support/Patient Care</div>
<div>Schedule:</div><div>
Night Shift</div>
<div>Employment Type:</div><div>
Full Time</div>
</div>
<div><div>Schedule: 36 Hours | Day or Night Shift Available
Sibley Memorial Hospital, a member of Johns Hopkins Medicine, has a distinguished history of serving the community since its founding in 1890. As a not-for-profit and full-service community hospital, Sibley offers medical, surgical, intensive care, obstetric, oncology, orthopedic and skilled nursing inpatient services, as well as a 24-hour Emergency Department. Sibley&rsquo;s campus is also home to Grand Oaks, an assisted living residence, a medical building with physician offices and ambulatory surgery and imaging centers.

The Patient Care Tech will provide nursing support for The Renaissance, a 45 bed skilled nursing/rehab facility at Sibley Memorial Hospital.

The Clinical Technician (PCT) works as a Certified Nursing Assistant (CNA) with advanced training in specific clinical skills/competencies on the health care team.
<ul>
<li>Periodically checks patients, takes vital signs, and observes condition of the patient and patient care equipment or devices.
</li><li>Provides personal care for patient including hygiene and physical comfort measures</li>
<li>Performs bedside glucose monitoring, EKG tracing, and phlebotomy</li>
<li>Inserts IVs
</li><li>Measures and records intake and output</li>
<li>Inserts and removes Foley catheters</li>
</ul>
What Awaits You:
<ul>
<li>Career growth and development</li>
<li>Tuition assistance</li>
<li>Free onsite parking</li>
<li>Up to 26 dayspaid leave upon employment</li>
<li>Affordable and comprehensive benefits package - Sibley Memorial Benefits</li>
<li>Free employee gym</li>
</ul>
Minimum Education and Experience:
<ul>
<li>High school graduate or GED</li>
<li>Current certification as CNA in the District of Columbia</li>
<li>Minimum 2 years patient care experience required</li>
<li>American Heart Association BLS/CPR required</li>
</ul>
Important Notices:
***Authorization to Work in the United States: Applicants who require sponsorship now or in the future will not be considered for this position.
Salary Range: Minimum 21.44/hour - Maximum 33.24/hour. Compensation will be commensurate with equity and experience for roles of similar scope and responsibility. In cases where the range is displayed as a $0 amount, salary discussions will occur during candidate screening calls, before any subsequent compensation discussion is held between the candidate and any hiring authority.

We are committed to creating a welcoming and inclusive environment, where we embrace and celebrate our differences, where all employees feel valued, contribute to our mission of serving the community, and engage in equitable healthcare delivery and workforce practices.

Johns Hopkins Health System and its affiliates are drug-free workplace employers.
</div>
</div>Johns Hopkins Health System and its affiliates are an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity and expression, age, national origin, mental or physical disability, genetic information, veteran status, or any other status protected by federal, state, or local law.</div><div></div>

Patient Care Technician - PCT - Rehab

Gerald Family Care PC

Overview We are seeking a dedicated and highly skilled Medical Doctor (MD)/Doctor of Osteopathic Medicine (DO) to join our dynamic healthcare team. In this vital role, you will provide comprehensive medical care across diverse specialties, ensuring optimal patient outcomes through expert diagnosis, treatment, and ongoing management. Your expertise will contribute to a compassionate, efficient, and innovative healthcare environment where patient well-being is at the forefront. This paid position offers an exciting opportunity to make a meaningful difference in patients&rsquo; lives while working within a collaborative clinical setting.Duties<ul><li>Conduct thorough patient assessments including physical examinations, medical history reviews, and diagnostic evaluations to determine health status and treatment needs.</li><li>Develop and implement personalized care plans utilizing evidence-based practices across various medical disciplines such as internal medicine, pediatrics, cardiology, neurology, and more.</li><li>Performing history and physical exam, ordering appropriate lab tests, radiology studies and screening studies via Face-to-Face (F2F), and Telehealth appointments.</li><li>Developing a treatment and follow-up plan to include medication, medical equipment, and home-based interventions</li><li>Evaluate and treat acute and chronic health problems for scheduled and unscheduled patients in the clinic setting</li><li>Records patient encounters, notes, orders, and consults appropriately and in a timely manner</li><li>Performs office procedures contained within their privileges</li><li>Communicates test results to patients</li><li>Assist in preparation of the patient and/or his/her family to include, but not limited to, teaching (to include health promotion and disease prevention activities), accumulating data and medical problems, and presenting patient centered discussion</li><li>Utilize Electronic Health Record (EHR) and EMR systems like eClinical Works (eCW) to document patient encounters accurately, track progress, and coordinate care seamlessly .</li><li>Collaborate with multidisciplinary teams including nurses, specialists in radiology, pathology, psychiatry, and other fields to deliver comprehensive patient care.</li><li>Stay current with advancements in medical technology such as CT scans, nuclear medicine, and diagnostic radiology to enhance treatment strategies.</li></ul>Skills<ul><li>Extensive knowledge of medical terminology, physiology, and anatomy essential for accurate diagnosis and effective treatment planning.</li><li>Experience in various specialties including but not limited to psychiatry, endocrinology, cardiology, nephrology, pulmonology, dermatology, immunology, oncology, obstetrics/gynecology (Ob/Gyn), neonatology, pediatrics and infectious disease care is a plus</li><li>Familiarity with healthcare protocols including HIPAA compliance for patient privacy and safety standards aligned with NCQA standards.</li><li>Competence in managing chronic conditions while addressing acute pain management needs or post-operative recovery.</li><li>Join us to be part of a forward-thinking healthcare team committed to delivering exceptional patient service through expertise across multiple specialties!</li></ul>Job Types: Full-time, Part-timePay: $190,000.00 - $222,000.00 per yearExpected hours: 24.0 &ndash; 40.0 per weekBenefits:<ul><li>Health insurance</li><li>Life insurance</li><li>Malpractice insurance</li><li>Paid time off</li><li>Visa sponsorship</li></ul>Application Question(s):<ul><li>Board-certified/board-eligible in Family Medicine, Internal Medicine or Pediatric Medicine required</li></ul>Experience:<ul><li>Family, Internal or Pediatric Medicine: 1 year (Preferred)</li></ul>Language:<ul><li>English (Preferred)</li></ul>Work Location: In person

Medical Doctor

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