Your impact 

As the PKPD Lead, you will develop the quantitative pharmacology strategy of drug discovery projects to deliver high quality clinical candidates, whilst using and contributing to the optimisation of state-of-the-art computational and AI drug design models. As part of the DMPK and Quantitative Pharmacology team, you will champion the use of model-informed drug discovery and development on both small molecule and biologics projects. You will work closely with the Biologics Discovery team to further develop AI models for biologics developability.

If you are an experienced and ambitious scientist looking to play an active part in the AI-driven transformation of the pharmaceutical industry, joining Isomorphic Labs will lift you out of your comfort zone and provide an amazing opportunity for personal growth and development.

What you will do 

PKPD Lead

• Design and implement quantitative pharmacology strategies with an AI-first approach, from target identification to pre-clinical development.
• Provide scientific leadership and integrate PK and quantitative pharmacology strategies for biologics projects, within the broader project strategy. As a member of the project core team, you will collaborate closely with colleagues in Drug Design, Pharmacology, ML Engineering, and Preclinical and Clinical Development to resolve PK and PD challenges.
• Develop advanced PKPD models for biologics and small molecule projects in collaboration with the DMPK and Pharmacology Leads.
• Contribute to the choice of modality that is the most appropriate for each target. Develop the target molecule profile at the inception of the project.
• Integrate PK, PD and toxicological data to extract decision-making information through mechanistic and empirical models, including dose and safety margin predictions for biologics projects.
• Author PKPD sections of regulatory documents.

ML interactions

• Partner with Machine Learning colleagues to integrate PK and PD aspects of the drug design platform and identify, generate and analyse data from which to develop and improve predictive models.
• Identify state-of-the-art integration methods that could bring transformational benefits to our platform or ways of working.
• Support the development of the biologics developability platform by identifying high-throughput techniques to predict the PK behaviour of various biologics formats.

CRO interactions

• Since IsomorphicLabs outsource all wet-lab work to external vendors, you will maintain and develop close relationships with the CRO network to:
• Ensure high quality and timely data generation to support our portfolio projects.
• Leverage the scientific expertise of our external collaborators to enhance the team's impact.
• Oversee the delivery of data generation campaigns purposefully designed to support the development of AI-based developability models.

People

• Mentor junior members of the DMPK and Quantitative Pharmacology  team.
• Embrace and champion a culture of inclusion and continuous professional development.

Skills and qualifications 

Essential:

• PhD in either Pharmaceutical Science, Pharmacy, or Chemistry or another relevant subject.
• 3+ years of related experience in the pharmaceutical industry.
• Experience as a PKPD Lead, solving PKPD-related problems in biologics projects with a track record of working collaboratively to deliver high quality candidates.
• Practical experience developing high quality quantitative pharmacology packages to support early clinical development, including authoring and reviewing regulatory documents, ideally in oncology.
• Advanced knowledge of PK and PKPD modelling for biologics.

Nice to have:

• Good understanding of machine learning techniques.
• Familiarity with Python and KNIME.

About the DMPK and Quantitative Pharmacology team

The DMPK and Quantitative Pharmacology team, part of the Preclinical Development group, accelerates the delivery of high quality drug candidates by developing innovative and creative AI-first solutions. By applying our domain expertise and through collaboration with the entirety of our world-class drug discovery disciplines and ML researchers, we ensure that drug-like properties are at the heart of our drug design engine. We shape the development of state-of-the-art ADME and toxicology predictive models. We rethink drug discovery from Hit ID to first-in-human (FIH) trials by optimising the context of use of these models.

Your impact

At Isomorphic Labs, DMPK Leads drive the DMPK strategy of drug discovery and development projects to deliver high quality clinical candidates whilst using and contributing to the optimisation of state-of-the-art computational and AI ADME models. 

As part of the Drug Design and Medical Research team and through close collaboration with the Technology teams, you will support the business alongside world leading AI/ML Drug Design Platform teams. You will collaborate to deliver scientific expertise and strategic direction to drive both improvements in the Platform and apply this to real drug design projects. You use your expertise in PBPK modelling to make data integration a powerful tool to accelerate drug design and preclinical development.

If you are a skilled and ambitious scientist looking to take the next step in your career, joining the Isomorphic Labs now will lift you out of your comfort zone and provide you with an amazing opportunity for personal growth and development.

What you will do 

• Define Iso’s PBPK strategy leading to fit for purpose models that drive drug design and accelerate accelerate preclinical development.
• Design and implement stage-appropriate development DMPK strategies with AI-first approach, integrate the quantitative pharmacology and overall project strategies.
• Design mechanistic experiments to support project progression in a data-driven manner.
• Integrate DMPK, PD and toxicological data to extract decision-making information, including dose and safety window predictions.
• Define Quantitative Pharmacology strategy in collaboration with Pharmacology Leads.
• Optimise molecule design and formulation based on physico-chemistry and biotransformation knowledge in collaboration with Chemistry Leads.
• Maintain knowledge of state-of-the-art technologies and methods to increase confidence in human PK prediction.
• Author DMPK sections of regulatory documents.
• Embrace and champion a culture of inclusion and continuous professional development.
• Optimise the use of Iso’s datasets to address fundamental DMPK questions and advance the field.

Skills and qualifications 

Essential:

• PhD in either Pharmaceutical Science, Pharmacy, Chemistry, or another relevant subject.
• 5+ years’ professional as a DMPK Lead, solving DMPK-related problems in preclinical development with a track record of working collaboratively to deliver regulatory-ready FIH packages.
• Practical experience in setting up automated PBPK workflows.
• Practical experience in using PBPK to support preclinical development.
• Practical experience developing DMPK and quantitative pharmacology packages to support early clinical development, including authoring and reviewing regulatory documents, ideally in oncology.
• Advanced knowledge of PK and PKPD modelling.
• Experience of partnering closely with Preclinical and Clinical teams.

Nice to have:

• Experience with biologics, peptides and other new modalities.
• Good understanding of machine learning techniques.
• Familiarity with Python and KNIME.

About the DMPK and Quantitative Pharmacology team

The DMPK and Quantitative Pharmacology team, part of the Preclinical Development group, accelerates the delivery of high quality drug candidates by developing innovative and creative AI-first solutions. By applying our domain expertise and through collaboration with the entirety of our world-class drug discovery disciplines and ML researchers, we ensure that drug-like properties are at the heart of our drug design engine. We shape the development of state-of-the-art ADME and toxicology predictive models. We rethink drug discovery from Hit ID to first-in-human (FIH) trials by optimising the context of use of these models.

Your impact

At Isomorphic Labs, DMPK Leads drive the DMPK strategy of drug discovery projects to deliver high quality clinical candidates whilst using and contributing to the optimisation of state-of-the-art computational and AI ADME models. 

As part of the Drug Design and Medical Research team and through close collaboration with the Technology teams, you will be supporting the business alongside world leading AI/ML Drug Design Platform teams. You will collaborate to deliver scientific expertise and strategic direction to drive both improvements in the Platform and apply this to real drug design projects. 

If you are a skilled and ambitious scientist looking to take the next step in your career, joining Isomorphic Labs will lift you out of your comfort zone and provide you with an amazing opportunity for personal growth and development.

What you will do 

• Design and implement stage-appropriate DMPK strategies with AI-first approach, integrating quantitative pharmacology and overall project strategies.
• Design screening cascade and mechanistic experiments to support project progression in a data-driven manner.
• Integrate DMPK, PD and toxicological data to extract decision-making information, including dose and safety window predictions.
• Define Quantitative Pharmacology strategy in collaboration with Pharmacology Leads.
• Optimise the use of Iso’s datasets to address fundamental DMPK questions and advance the field.
• Optimise molecule design based on physico-chemistry and biotransformation knowledge in collaboration with Chemistry Leads.
• Maintain knowledge of state-of-the-art technologies and methods to increase confidence in human PK prediction.
• Author DMPK sections of regulatory documents.
• Embrace and champion a culture of inclusion and continuous professional development.

Skills and qualifications 

Essential:

• PhD in either Pharmaceutical Science, Pharmacy, Chemistry, or another relevant subject.
• 3+ years’ professional experience as a DMPK Lead, solving DMPK-related problems in drug discovery with a track record of working collaboratively to deliver high quality candidates.
• Practical experience developing DMPK and quantitative pharmacology packages to support early clinical development, including authoring and reviewing regulatory documents, ideally in oncology or immunology.
• Experience of partnering closely with Preclinical and Clinical teams.
• In depth knowledge of biotransformation.
• In depth knowledge of PK modelling and scaling of ADME properties.

Nice to have:

• Experience with biologics, peptides and other new modalities.
• Advanced knowledge of PKPD modelling.
• Good understanding of machine learning techniques.
• Familiarity with Python and KNIME.

The Team You’ll Join 

As part of Recursion's Value Tech Tooling Team, you will be at the forefront of reimagining drug discovery from first principles using our massive data capabilities. You'll work in a cross-functional team of world-class computational biologists and engineers who turn complex analyses and data workflows into stable tools and pipelines that multiply their impact and industrialise the discovery process across a wide array of therapeutic areas. You'll partner with biologists, medicinal chemists, engineers, data scientists, ML scientists, and to design experiments, develop new methods, build scalable data workflows, analyse results, and identify common themes across programs. As our toolbox grows and evolves, it will contribute to a revolution in drug discovery to bring life-changing therapeutics to patients at greater speed and with higher quality, safety and efficacy than ever before.

In this role, you will:

• Synthesize, integrate, and analyse diverse internal and external datasets from computational biology, target discovery, functional genomics, biomarker discovery, and real-world and clinically derived data sources, and identify commonalities to turn into reusable tools and pipelines.
• Build, maintain, and improve robust data pipelines and analytical workflows for complex biological datasets, including omics data, internally generated biological assay data, and external data sources such as Tempus and other real-world datasets.
• Develop and apply agentic workflows to integrate and orchestrate analyses across multiple internal and external data sources, accelerating insight generation and supporting scalable decision-making across drug discovery programs.
• Partner with engineers to mature pilot tooling and workflows into stable products and infrastructure that multiply the effectiveness of scientific collaborators pursuing drug programs.
• Present and discuss data, pipelines, and tools with decision makers and stakeholders in a clear and compelling way that drives toward getting medicines to patients.
• Collaborate cross-functionally with Recursion’s platform data science, data engineering, and ML teams to further advance Recursion’s ability to interpret and translate large-scale phenomics and multimodal data into therapeutic programs.

The Experience You’ll Need

• PhD in a relevant field (e.g., computational biology, bioinformatics, statistics, quantitative pharmacology, cancer/cell biology, computer science, or a related discipline), or equivalent experience, with a track record of applying these skills to fundamental problems in drug discovery.
• Experience applying computational methods (including statistical, probabilistic, and/or machine learning techniques) to analyse complex biological and/or human clinical data.
• Experience building, maintaining, and improving reproducible data pipelines and analytical workflows for large, heterogeneous biological datasets (Python strongly preferred).
• Experience working with high-dimensional biological datasets, including omics data (e.g., single-cell and other genomics-based modalities) and/or other complex assay modalities.
• Experience turning exploratory analyses into reusable tools, workflows, and documentation that can be adopted by other scientists/teams.
• General understanding of drug discovery and translational biology.

Nice To Have

• Experience working on highly collaborative cross-functional teams; ability to clearly explain computational analyses, data workflows, and methodologies to cross-functional and non-technical teams.
• Hands-on experience working with real-world clinical datasets (EHR/claims/registries) and/or generating real-world evidence (cohorting, endpoint definition, observational study considerations).
• Experience with real-world clinical datasets (e.g., EHR-derived oncology datasets) or demonstrated ability to rapidly learn new healthcare data modalities; experience with Tempus or similar datasets is a plus.
• Experience integrating multimodal datasets (e.g., genomics + phenomics, genomics + imaging) in service of translational decisions.
• Experience developing or applying agentic workflows to orchestrate analyses across multiple internal and external data sources, accelerating insight generation and decision-making

Working Location & Compensation:

This is an office-based, hybrid position at our office located in London, England. Employees are expected to work in the office at least 50% of the time.

At Recursion, we believe that every employee should be compensated fairly. Based on the skill and level of experience required for this role, the estimated current annual base range for this role is £86,300 - £115,500. You will also be eligible for an annual bonus and equity compensation, as well as a comprehensive benefits package. 

#LI-EP1

Band 7 Lead Pharmacy Technician – Procurement & Distribution

Banding: Band 7
Location: Cross‑site – Epsom & St Helier University Hospitals NHS Trust
Start Date: ASAP
Duration: Ongoing
Hourly Rate: £28–£34 per hour (DOE)
Working Hours: 37.5 hours, Monday–Friday (with late duty, weekend & bank holiday cover on rotation)

Job Overview

Pulse is now recruiting for an experienced Band 7 Lead Pharmacy Technician – Procurement and Distribution to join a forward‑thinking NHS Pharmacy department.
This role is essential in ensuring the safe, effective and efficient delivery of medicines procurement, storage, stock control and distribution Trust‑wide.

You will provide professional leadership to the procurement and distribution teams, manage pharmacy purchasing operations, and support the ongoing development of the pharmacy computer systems (CMM). The role requires strong operational leadership skills, excellent organisational ability and experience managing complex supply chains in a hospital setting.

Key Responsibilities

Leadership & Management

• Provide leadership for procurement and distribution services across the Trust.
• Line manage Procurement Officers, Technicians and Stores staff.
• Lead on performance management, appraisals, training and service development.
• Support the Chief Technician for Procurement & Computer Services, deputising when required.

Procurement & Supply

• Oversee day‑to‑day purchasing, invoice queries, supplier liaison and contract compliance.
• Ensure cost‑effective purchasing practices and accurate stock control.
• Resolve drug shortages, substitutions, and supplier issues.
• Ensure safe management of unlicensed medicines and all associated documentation.
• Maintain data accuracy on the CMM pharmacy system and support future system developments.

Distribution & Stores

• Oversee safe storage, stock rotation, expiry checks and delivery processes.
• Ensure medicines are distributed efficiently and in line with Trust policies.
• Support audits, governance, quality assurance and risk management processes.

Quality, Governance & Safety

• Ensure compliance with medicines legislation, procurement guidance and financial governance.
• Investigate errors, incidents and complaints using root‑cause analysis.
• Support medication safety processes, optimisation work and formulary compliance.

Training & Development

• Train and mentor pharmacy staff, including technicians and assistants.
• Support NVQ programmes, induction and competency‑based training.
• Provide teaching sessions on procurement and distribution processes.

Qualifications & Experience

Essential:

• BTEC/NVQ Level 3 in Pharmaceutical Science (or equivalent).
• GPhC registered Pharmacy Technician.
• Significant post‑registration experience within hospital pharmacy.
• Experience in procurement, distribution or purchasing services.
• Experience using the CMM Pharmacy System.
• Strong leadership/supervisory experience.
• Understanding of finance systems, stock control and budget processes.
• Excellent communication, IT competence and organisational skills.

Desirable:

• Accredited Checking Technician qualification.
• Post‑registration management qualification.
• NVQ assessor or Educational Supervisor training.
• Knowledge of procurement regulations and contract management.

Why Choose Pulse?

• Daily payroll
• Free DBS & compliance
• Free mandatory training
• Exclusive NHS & private sector roles
• Dedicated consultant support
• Fast‑track registration
• Support with CPD & revalidation
• £300 recommend‑a‑friend bonus

How to Apply

If you're interested in this role, please contact the Pharmacy team at Pulse AHP.
Apply now or email your CV and availability.

Reasonable Adjustments

Pulse is committed to supporting individual needs. If you require adjustments during the recruitment process or while working with us, please let us know.

International Applicants

Please note: Pulse cannot currently offer visa sponsorship. Applicants must have the Right to Work in the UK.

Band 7/8a Clinical Pharmacist

Banding: Band 7 or 8a
Location: Calderdale Royal Hospital (CRH) or Huddersfield Royal Infirmary (HRI)
Start Date: ASAP
Duration: Ongoing
Hourly Rate: £30–£35 per hour (DOE)
Working Hours: Monday–Friday, 08:30–17:00 (occasional requirement to work until 18:00)

Job Overview

Pulse is now recruiting for an experienced Band 7 or 8a Clinical Pharmacist to join the Clinical Pharmacy Service at Calderdale and Huddersfield NHS Foundation Trust.
This is an excellent opportunity to deliver high‑quality medicines optimisation, provide expert clinical input, and support multidisciplinary teams across a range of clinical settings.

You must have strong clinical knowledge, excellent communication skills, and the ability to work both autonomously and within a wider team.

Key Responsibilities

Clinical Duties

• Review prescriptions for clinical appropriateness, legality, and potential drug interactions.
• Dispense and supply medications in line with Trust and legal standards.
• Provide clinical and professional advice to medical, nursing, AHP and pharmacy staff, as well as patients and carers.
• Make evidence-based clinical recommendations, including dose adjustments and complex drug calculations.
• Manage medication decisions for patients with renal/hepatic impairment, co‑morbidities, or concurrent therapies.
• Advise in high‑risk areas such as IV therapy, pregnancy, and breastfeeding.
• Use professional judgement to manage complex clinical scenarios where definitive information may be limited.
• Participate in pharmacy audits, research, and quality‑improvement activities.
• Support antimicrobial stewardship in collaboration with microbiology and antibiotic pharmacists.
• (If qualified) Prescribe independently within your area of competence.

Professional Duties

• Implement Trust Medicines Management and medication safety policies.
• Undertake duties of the Responsible Pharmacist when required.
• Contribute to staff training, supervision, and education of pharmacy students and wider healthcare colleagues.
• Maintain up‑to‑date CPD in line with GPhC requirements.
• Work flexibly across CRH, HRI and other Trust sites where needed.

Qualifications & Experience

Essential:

• MPharm or equivalent degree approved by the GPhC
• GPhC registered Pharmacist
• Postgraduate Diploma in Clinical Pharmacy (or equivalent)
• Minimum 1 year pre‑registration training
• Strong clinical pharmacy and medicines management knowledge
• Understanding of medicines governance
• Computer literate – ideally with experience using Cerner and EMIS
• Experience in clinical audit and/or pharmacy practice research
• Ability to work under pressure, prioritise workload and meet deadlines
• Ability to work both independently and as part of a team
• Commitment to ongoing CPD
• Eligibility to work in the UK
• Ability to work across multiple Trust sites

Desirable:

• Independent Prescriber qualification

Why Choose Pulse?

• Daily payroll
• Access to exclusive NHS and private sector roles
• Dedicated consultant support (Mimi!)
• Free mandatory training
• Free DBS/Compliance
• Streamlined registration process
• Support with revalidation & CPD
• £300 recommend‑a‑friend bonus scheme

How to Apply

If you’re interested in this role, please contact the Pharmacy team at Pulse AHP.
Apply now or email your CV and availability.

Reasonable Adjustments

If you require any reasonable adjustments during the recruitment process or while working with Pulse, please let us know—we are committed to supporting your needs.

International Applicants

Please note: At this time, Pulse is unable to support visa sponsorship for international applicants. You must have the Right to Work in the UK.

Job overview:  

The Clinical Scientist, Clinical Sciences will assist with the clinical development and scientific oversight of late stage clinical trials.

The role partners closely with Clinical Operations, Statistics, Data Management, Clinical Safety, Regulatory Sciences, and HEOR to deliver high-quality studies, enabling timely, compliant, and insight-driven decision making.

Location: Hybrid in our Soho London office or remote in the United Kingdom.

Reports to: Principal Clinical Scientist, Clinical Sciences.

Duration: Until the end of 2026.

Roles and responsibilities 
(Include but are not limited to): 

• Serve as the primary “point person” for assigned clinical research duties
• Support scientific oversight during study execution, supporting database design, medical monitoring, site initiation visits, protocol deviation review and clarification, and interpretation of clinical signals across programs
• Author and review participant-facing documents such as the informed consent form and advertisement material
• Support development of study conduct and statistical analysis plans; review data to ensure quality of study conduct and data collection
• Accountable for compliance with ethical and scientific standards, regulatory requirements, and the Compass Quality Management System, ensuring participant safety, data integrity, and accuracy throughout the trial process
• Contribute to cross-functional readiness for key milestones (database lock, regulatory documents), establishing operating rhythms and documentation standards consistent with Compass values and governance
• Champion patient-centric design, incorporating feasibility data, KOL feedback, and ethical considerations into procedures, visit schedules, and burden-reduction strategies

Candidate Profile:

• A PhD or PharmD is highly preferred but not required. MS candidates with equivalent experience also will be considered
• PhD or post-doctoral training should be in neuroscience, pharmacology, psychology, psychiatry, or other relevant biomedical science
• PharmD graduates should have training in research methods or postdoctoral research experience as above
• MS graduates should demonstrate scientific accomplishment comparable to that acquired in doctoral training as above
• Relevant experience in conducting and designing clinical research in neuroscience, pharmacology, psychiatry, or neurology
• Proven capability to translate biology and patient insights into clear study objectives, endpoints, and operationally feasible designs
• Strong analytical and statistical skills, experience authoring scientific documents, and well-developed communication skills appropriate to varying target audiences
• Excellent scientific writing, data interpretation, and communication skills, with a track record of high-quality clinical documents and timely milestone delivery
• Mission-aligned, inclusive contributor who reflects Compass values and a wellbeing-first, stigma free culture

The Role

We are looking for an ambitious, clinically grounded retina specialist to join our growing ocular gene therapy team as a Medical Director. This is a unique opportunity for an early-career retina specialist to play a visible, high-impact role in advancing transformative therapies for inherited retinal diseases (IRDs).

In this role, you will help shape clinical strategy while staying close to the science and the patients. You will work at the intersection of clinical medicine, imaging, and innovative gene therapy development—contributing meaningfully to programs from early development through late-stage trials.

What makes this role compelling:

• Direct impact on cutting-edge gene therapy programs in IRDs
• High visibility across clinical, regulatory, and scientific functions
• A role that leverages your clinical and imaging expertise—not just oversight

If you are a candidate with strong hands-on experience in retinal disease management and imaging, we encourage you to apply.

Key Responsibilities: 

• Contribute to and help shape clinical development strategy across ocular gene therapy programs, from early-phase through late-stage studies
• Support the design and execution of clinical trials (Phase 1–3), including protocol development, amendments, and benefit–risk assessment
• Apply deep clinical and imaging expertise to review and interpret retinal imaging (e.g., OCT, fundus autofluorescence) for patient selection, endpoint evaluation, and data interpretation
• Lead ongoing medical data review, including eligibility assessments and continuous evaluation of aggregated safety and efficacy data during trial conduct
• Provide medical oversight of safety events, including review of serious adverse events and development of safety narratives
• Ensure compliance with Good Clinical Practice (GCP) and applicable regulatory requirements across all clinical activities
• Contribute to the preparation and review of key clinical and regulatory documents (e.g., protocols, CSRs, briefing books, clinical sections of submissions)
• Collaborate closely with clinical operations on feasibility, site selection, enrollment strategy, and trial execution
• Serve as a key medical partner to investigators, sites, and key opinion leaders, providing scientific guidance and clinical support
• Translate clinical and imaging insights into clinical development decisions, including endpoint selection and overall program strategy
• Work cross-functionally with translational science, regulatory, and other stakeholders to ensure high-quality, efficient study delivery

Education and Qualifications: 

• MD or MD/ PhD with ophthalmology
• Retina subspecialty training with expertise in retinal imaging is strongly preferred
• Experience in inherited retina diseases is desirable.
• Experience in translational drug development in the pharmaceutical or biotechnology industry will be a plus.

Skills and Capabilities:

• High ethical standards and commitment to patient-centric drug development
• Strong clinical expertise in retinal diseases, with demonstrated proficiency in retinal imaging interpretation
• Outstanding attention to detail, particularly in the context of imaging review, data interpretation, and clinical trial conduct
• Willingness to learn about clinical development and broader drug development process
• Ability to collaborate across functions
• Ability to prioritize and manage multiple deliverables in a dynamic environment
• Strong interpersonal and communication skills, with the ability to build relationships and influence cross-functional teams and external stakeholders
• High-quality presentation and publication skills demonstrated by first author scientific presentations and publications
• Sound judgment and decision-making skills, balancing scientific rigor, patient safety, and program needs
• Strong team orientation, with a collaborative and proactive mindset

The Opportunity

As a Radiologic Technologist (RT), you’ll play a vital role in our mission to provide high-quality care by combining your radiology expertise with hands-on clinical support. In our fast-paced urgent care clinics, you’ll work closely with a collaborative team to make a meaningful difference in patients’ lives, ensuring they receive accurate diagnoses and the best possible treatment. 

If you’re passionate about patient care and thrive in a dynamic environment, we’d love to have you join our team! 

Be sure to ask your recruiter about our competitive sign-on bonus opportunities for full-time team members!

Your Impact 

• Radiologic Procedures & Imaging: Prepare and perform radiologic procedures following ConvenientMD and ARRT protocols.
  • Operate radiographic, fluoroscopic, and portable equipment, ensuring proper radiation safety and adhering to ALARA principles.
  • Position patients for optimal imaging and completed document studies in EMR and PACS.
  • Collaborate with radiologists for study interpretation, manage discrepancies, and coordinate outside imaging requests.
• Clinical Support: Efficiently switch between RT and Medical Assistant responsibilities.
  • Conduct patient triage, including vital signs, medical history, and observational examination.
  • Provide laboratory and diagnostic testing, screenings, and treatment for acute and chronic illnesses.
  • Perform a variety of testing procedures, including vision, hearing, drug screening, pulmonary function testing, and point-of-care diagnostics (e.g., strep, flu, RSV, glucose, urinalysis).
  • Maintain clean, sterile exam rooms and instruments to ensure a safe clinical environment.
• Patient Interaction: Support clinical care standards by adhering to ConvenientMD policies and delivering compassionate, patient-centered care.   
• Quality Assurance & Inventory Tracking: Manage radiology supply inventory and submit orders as needed.
  • Ensure medical equipment is operational through preventive maintenance and timely repairs.
  • Participate in quality control and assurance studies to uphold clinical standards.
  • Maintain accurate records, files, and documentation in alignment with HIPAA and ConvenientMD protocols.
• Team Collaboration & Training: Support onboarding and training for new clinic team members.
  • Foster a positive work environment by collaborating with colleagues to deliver high-quality care.
  • Communicate effectively with team members and external providers to ensure seamless patient care. 

Who You Are 

• Education, Licensure, & Certifications:
  • High school diploma or GED required.
  • State licensed with the American Registry of Radiologic Technologist (ARRT).
  • American Heart Association or American Red Cross BLS certification. We do not accept CPR, ACLS certifications, or online only classes. 
• Experience: 1-2 years in radiology and patient care, preferably in urgent care or emergency settings.
• Compassionate, authentic, and patient focused: Supports patients through kindness; demonstrating understanding for others and contributing to the creating a community of belonging.
• Proactive and confident communicator (written and verbal): Foreshadows and elevates concerns as they arise, unafraid of professional directness both with colleagues and patients.
• Excellent team player: You enjoy collaborating with others and being a part of a strong team dynamic.
• Technically savvy: Proficient with Microsoft Office Suite or related software. Must be able and willing to navigate and learn multiple systems.
• Driven and self-motivated: Capable of working independently, possess a level of initiative and enthusiasm to help drive results. Actively identifying better ways of working. Uses resources to achieve the best outcomes for patients, the team, and the organization.
• Trustworthy: Ability to maintain confidentiality and handle all patient information in accordance with HIPAA regulations.