Clinical Application Specialist Jobs

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds... We are building our talent pipeline for 2027 and expect to have multiple opportunities throughout the year for experienced professionals in Clinical Statistical Programming at the Senior and Principal level. We anticipate hiring for up to 20 positions during calendar year 2027, with openings becoming available at different times based on client demand and business growth. The Senior/Principal Statistical Programmer is responsible for serving as a technical and study programming lead across multiple compounds and/or studies within the Statistical Programming function, supporting Ipsen’s assets within a specific therapeutic area such as Oncology, Rare Disease, or Neuroscience . The role requires strong hands-on statistical programming expertise, study leadership, and technical knowledge to ensure the quality, consistency, and timely delivery of statistical programming activities. The programmer will work closely with statisticians, clinical teams, data management, and other cross-functional stakeholders and may also provide technical oversight of outsourced programming activities. Main Responsibilities & Technical Competencies Serve as a lead statistical programmer for multiple studies and/or compounds, ensuring high-quality and timely delivery of statistical programming activities. Lead and execute statistical programming activities across clinical trials, from study start-up through database lock, reporting, and regulatory submission. Ensure consistency, quality, and executional excellence across programming deliverables for assigned studies. Support programming activities for global regulatory submissions and responses to health authority questions. Provide technical oversight and guidance for outsourced statistical programming activitie

Non-Medical Prescriber (ADHD) | Associate Clinician Location: Remote Job Type: Associate / Session-Based Pay: Competitive sessional rates Organisation: Xyla Neurodevelopmental Services (Xyla ND) About the Role Xyla ND is expanding its prescribing workforce to meet increasing demand for ADHD assessments and ongoing treatment support. We are seeking experienced Non-Medical Prescribers (NMPs) who can work independently to assess, diagnose, prescribe, and manage patients with ADHD. This is an excellent opportunity for clinicians looking for flexible, sessional work alongside existing commitments. Initial volumes will be low, with opportunities for increased work as demand grows. Key Responsibilities Conduct ADHD suitability and assessment appointments Prescribe medication where clinically appropriate Manage patient titrations and medication reviews Complete all required clinical documentation and administration Undertake annual review appointments for existing patients Work independently within professional and regulatory guidelines Essential Requirements Qualified Non-Medical Prescriber (NMP) Able to independently assess and prescribe for ADHD patients Minimum 2 years' experience assessing and prescribing for ADHD Meets required DIVA assessment experience standards Able to provide evidence of DIVA assessment experience Comfortable undertaking low-volume assessment work initially Excellent clinical judgement and report-writing skills Session Rates Initial Suitability Appointment 45-60 minutes Includes prescribing (where clinically appropriate), administration, and prescription postage £80 per appointment Titration Appointments Three monthly review sessions 40 minutes per appointment (30-minute consultation + 10 minutes administration) £40 per appointment Annual Review Appointments 55 minutes per appointment (45-minute consultation + 10 minutes administration) £40 per appointment Why Join Xyla ND? Fully flexible, session-based work Remote delivery Opportunity to s

We’re building a world of health around every individual — shaping a more connected, convenient and compassionate health experience. At CVS Health®, you’ll be surrounded by passionate colleagues who care deeply, innovate with purpose, hold ourselves accountable and prioritize safety and quality in everything we do. Join us and be part of something bigger – helping to simplify health care one person, one family and one community at a time. Program Overview: Help us elevate our patient care to a whole new level! Join our Aetna team as an industry leader in serving dual eligible populations by utilizing best-in-class operating and clinical models. You can have life-changing impact on our members, who are enrolled in Medicare and Medicaid and present with a wide range of complex health and social challenges. With compassionate attention and excellent communication, we collaborate with members, providers, and community organizations to address the full continuum of our members’ health care and social determinant needs. Join us in this exciting opportunity as we grow and expand to change lives in new markets across the country. This position is focused on assisting members in: Kankakee, Iroquois, Livingston, Ford, Champaign and surrounding counties. Position Summary/Mission: The Case Management Coordinator utilizes critical thinking and judgment to collaborate and inform the case management process. The Case Management Coordinator facilitates appropriate healthcare outcomes for members by providing assistance with appointment scheduling, identifying and assisting with accessing benefits and education for members through the use of care management tools and resources. Fundamental Components • Evaluation of Members: Through the use of care management tools and information/data

Job Title: Band 6 Biomedical Scientist – Biochemistry Banding: Band 6 Location: Surrey Rate: £22 - £26 per hour Start Date: ASAP Duration: Ongoing Working Hours: Full-time, including out-of-hours shifts, weekends, and Bank Holidays An exciting opportunity has arisen for an experienced Band 6 Biomedical Scientist to join a well-established NHS laboratory in Surrey. This role offers the chance to work within a busy Clinical Biochemistry service, supporting the delivery of high-quality diagnostic testing in a modern laboratory environment. What will your responsibilities be: • Perform routine and specialist Clinical Biochemistry investigations in accordance with departmental policies and procedures • Operate, maintain, and troubleshoot automated biochemistry analysers • Validate and authorise results within the scope of competency and laboratory protocols • Ensure accurate and timely processing of samples to support patient care • Participate in quality control, quality assurance, and audit activities • Maintain compliance with UKAS, ISO 15189, and departmental standards • Support service delivery across the department and contribute to continuous improvement initiatives • Participate in the laboratory's out-of-hours rota, including evenings, weekends, and Bank Holidays Qualifications and Experience: Essential: • HCPC registration as a Biomedical Scientist • Previous experience working within a Clinical Biochemistry laboratory • Competency using Abbott Alinity analysers and/or laboratory information management systems (LIMS) • Strong understanding of quality assurance and laboratory governance processes • Excellent organisational skills and the ability to prioritise workload effectively Desirable: • Previous Band 6 experience within Clinical Biochemistry • Experience working in a high-throughput NHS laboratory environment • Experience participating in an out-of-hours service rota Why work with Pulse? From the moment you registe

We’re building a world of health around every individual — shaping a more connected, convenient and compassionate health experience. At CVS Health®, you’ll be surrounded by passionate colleagues who care deeply, innovate with purpose, hold ourselves accountable and prioritize safety and quality in everything we do. Join us and be part of something bigger – helping to simplify health care one person, one family and one community at a time. Position Summary We are seeking a skilled and analytical Senior Product Analytics Associate to lead the development and execution of a data-driven product roadmap. The ideal candidate will have a deep understanding of product analytics, strong problem-solving skills, and experience working with cross-functional teams to support strategic initiatives. As a Senior Product Analytics Associate, you will work closely with cross-functional teams including engineering, product, and clinical operations. Roles and Responsibilities: Define, track, and report on product metrics including performance and profitability Build and maintain robust data transformation models using dbt (or similar frameworks like Dataform or SQL-based ETL tools) to ensure analytics-ready datasets Design and interpret A/B tests; when A/B testing is not feasible, apply causal inference methods (e.g., Diff-in-Diff, Propensity Score Matching) to determine product efficacy. Develop ROI projections for analytics projects to prioritize deliverables by business impact Tell compelling stories through data, articulating technical information to a non-technical audience Build and maintain Power BI dashboards to

Opportunity Overview: We're seeking a Senior Director, Solution Owner to join Cohere Health's PaaS Delivery organization. In this role, you will personally own the end-to-end success — business, clinical, and technical — of our most complex and highest-stakes customer implementations. You'll partner closely with Solution Architects, Forward Deployed Engineers, Platform Configuration, QA, and Technical Program Managers to set the standard for what great solution ownership looks like at Cohere, operating as a credible, executive-level counterpart to our clients' leadership. This is a remote-first role that may require travel to Boston, MA for new hire onboarding and occasional in-person team meetings and company events. What you’ll do: Own end-to-end success — business, clinical, and technical — for Cohere's largest and most complex customer implementations Apply strategic program leadership to multi-year, multi-workstream, enterprise-scale platform deployments Drive a team of SMEs toward on-time deployments through meticulous organization, program management, and timeline tracking Serve as the escalation point and executive-level counterpart to client leadership on flagship accounts Set the standard for what excellent solution ownership looks like at Cohere, through the quality of your own account work Make the call on the highest-stakes scope, timeline, and resourcing trade-offs, with direct visibility into business risk What you’ll need: 10+ years leading large-scale, complex technology or platform deployments, with significant healthcare experience Direct experience delivering large-scope products at healthcare companies — claims systems, utilization management/prior authorization platforms, or similarly complex, mission-critical systems Demonstrated strategic program leadership — has personally owned outcomes on the scale of a multi-year, multi-million dollar enterprise implementation Executive presence — credible and effective operating as a peer with clie

We are currently recruiting for an experienced Band 7 Cardiac MRI Radiographer to join an established imaging service. This is an excellent opportunity for an experienced MRI Radiographer with strong Siemens MRI experience and a background in Cardiac MRI , who is confident working across both specialist and general MRI examinations. The Role Perform Cardiac MRI examinations to a high clinical standard. Support the development and building of Cardiac MRI protocols . Undertake a range of general MRI examinations alongside cardiac work. Demonstrate strong knowledge of MRI safety procedures and protocols . Work confidently with Siemens MRI systems. Support the wider MRI team and contribute to the delivery of a high-quality imaging service. Work flexibly across standard day and long-day shifts . Essential Requirements Minimum 2 years’ MRI experience. Strong experience in Cardiac MRI . Extensive Siemens MRI experience . Competent across general MRI examinations . Strong understanding of MRI safety . Valid cannulation certificate from SOR or a recognised university . Ability to work flexibly across day and long-day shifts . HCPC registration as a Diagnostic Radiographer. Desirable Previous NHS experience . Experience with Soliton . Previous involvement in developing or building MRI protocols . Previous Band 7 or senior-level MRI experience.

TERRITORY: Dallas West to Forth Worth East We are looking for a high-energy, adaptable, and results-driven Account Sales Representative (ASR) to join our Women’s Health sales team in the Dallas West territory! In this role, you will drive market adoption and business growth by supporting direct sales to OB/GYNs and Maternal-Fetal Medicine (MFM) specialists. The Dallas West territory is a fast-paced environment with high growth potential. You will work in lockstep with a fast-paced Clinical Field Specialist (CFS) partner. The ideal candidate isn't just a support player—they are a quick learner, a proactive go-getter, and a "sales chameleon" who can build immediate trust, match their CFS’s rapid pace, and help grow the territory. Primary Responsibilities Drive Growth in current sending accounts: Work directly with your assigned CFS to execute strategic territory plans, target growth in current sending accounts and maintain them. Partner at Pace: Work in seamless alignment with a high-speed CFS partner. Match their urgency, learn on the fly, and absorb administrative and customer support tasks so the team can close business faster. Adaptable Customer Engagement: Act as a true account chameleon—effortlessly tailoring your communication style, clinical knowledge, and interpersonal approach to connect with everyone from head physicians and practice managers to medical assistance and other staff. Account Logistics & Support: Assess the needs of medical professionals and staff members with a relentless focus on customer support, sample/logistics coordination, and rapid problem-solving. Maintain & Protect Existing Business: Ensure existing accounts receive white-glove service to maintain high retention rates while introducing currently marketed products and supporting new product launches. Cross-Functional Communication: Work closely with internal

Omada Health is on a mission to bend the curve of chronic disease. Job overview: The Senior Program Manager, Health Coaching reports to the VP, Operational Excellence and serves as the business operations dyad partner to the Senior Director of Health Coaching & Practice. The Senior Program Manager leads Health Coaching’s strategy and business planning and data driven continuous-improvement efforts. They translate priorities into actionable operating plans, data-driven decisions, and measurable improvements in coach and member outcomes, operating performance, and cost to serve. The Senior Program Manager proactively partners with stakeholders across Health Coaching, Care Delivery, Clinical, and the broader company to advance business priorities and improve new and existing programs. They bring structure to complex business challenges by using data, performance metrics, and disciplined problem-solving to identify opportunities, clarify tradeoffs, inform decisions, and move cross-functional initiatives forward. Because this person will influence colleagues within Health Coaching, Care Delivery, and across Omada, they will demonstrate strong leadership skills, operate effectively through ambiguity, and be highly collaborative and organized. Your Impact: Management of strategic roadmap Document and manage business priorities, project governance plans, project schedules, success criteria and project milestones Develop solutions, identify owners, set delivery/completion dates and set up mechanisms to ensure programs are on track Proactively identify and resolve issues that affect Omada’s Care Teams and/or member experience and may impair our ability to meet strategic, programmatic or product goals. Actively build relationships across Omada teams to deliver on your roadmap. Partner with Care Delivery program managers as well as partners in Clinical, Strategic Finance, Legal, HR, and Engineering/Product/Design to deliver on your roadmap. Anticipate bottlenecks, mak

Senior Histopathology Biomedical Scientist Location: Oxfordshire Salary: £60,000 - £65,000 + Benefits Job Type: Permanent, Full-Time An exciting opportunity has arisen for an experienced Senior Histopathology Biomedical Scientist to join a well-established laboratory in Oxfordshire. This permanent role is ideal for an HCPC-registered Biomedical Scientist with significant Histopathology experience and strong specimen dissection skills who is looking to progress their career within a supportive and growing laboratory environment. What will your responsibilities be? Undertake Histopathology specimen dissection and cut-up in line with departmental procedures and professional scope of practice. Support the delivery of a high-quality Histopathology service within a busy laboratory environment. Maintain accurate specimen documentation and laboratory records. Contribute to quality assurance, audit readiness and compliance with UKAS requirements. Work independently while collaborating effectively with laboratory and clinical colleagues. Support service improvement and the development of junior team members where appropriate. Qualifications and Experience HCPC registration as a Biomedical Scientist. Extensive post-registration experience in Histopathology. Strong specimen dissection and cut-up experience. Previous experience working within NHS laboratory settings. Ability to work independently and support service delivery within a busy department. Strong understanding of UKAS accreditation and laboratory quality standards. Why work with Pulse? From the moment you register with us, our focus is entirely on you. During our first conversation, you’ll quickly see that we understand your speciality inside and out. Our expert recruitment consultants are dedicated to finding you the best opportunities and supporting you every step of the way to secure the right position. With preferred or sole supplier status with many clients, you’ll have access to exclusive opportunities that you

DeepIntent is the leading healthcare marketing platform, purpose-built to help marketers plan, activate, and optimize data-driven campaigns with speed and precision. Trusted by the world’s top healthcare brands and their agencies, DeepIntent uniquely unites media, identity, and real-world clinical data to power privacy-safe, omnichannel marketing across every screen. Backed by patented technology and proven outcomes, DeepIntent’s platform delivers measurable audience quality and script lift at scale. Learn more at www.deepintent.com . What You’ll Do: DeepIntent is looking for a Data Integrations Specialist to run our client data integrations. This is a highly client-facing role and with strong requirements for good project management skills. This position is to ensure DeepIntent provides a fast, transparent and error free integrations service to our agency and brand clients. Majority of integrations can be configured through the user interface, although some custom cases would require collaboration with backend engineers. Hands on experience with integrations management Manage target list handoffs Supporting existing/live integrations maintenance Acting as quarterback for organization of client discussions and implementations Manage custom PLD reports, work with clients to gather requirements, shepherd implementation with the DSP and custom scripts (where applicable) Collaborate with engineers on escalation cases Manage documentation process for all internal & client integrations Be clients’ main point of contact for all things integrations-related Who You Are: 3+ years of experience in programmatic advertising and/or publishing, supported by a strong analytical background Strong communication skills, confidently able to work in a client facing capacity Confidence to run agency & pharma client meetings Project management skills (must be able to spearhead and manage multiple projects at once) Requirements gathering: ability to partner

About Anthropic Anthropic’s mission is to create reliable, interpretable, and steerable AI systems. We want AI to be safe and beneficial for our users and for society as a whole. Our team is a quickly growing group of committed researchers, engineers, policy experts, and business leaders working together to build beneficial AI systems. About the Role Scientists use Claude across the life sciences, from drug discovery and research biology to clinical development and manufacturing. To support that work, Anthropic introduced the Life Sciences Verification Program (LSVP), which gives verified life science professionals access to Claude with a refined set of safeguards that is more permissive for biology-related work. The program is in beta.We're hiring a Technical Program Manager to own the program of work that expands that access and helps scale it with safety in mind. Each expansion depends on many teams at once and no single team owns the path end to end. You'll become the single owner of that program, the person who knows what each expansion requires, where every workstream stands, what it is waiting on, and who needs to decide. This is a cross-org execution role, not a research role, and it does not require a life sciences background. LSVP is the starting point, and the scope will grow alongside Anthropic's broader work in the life sciences. Over time, more of the life sciences community can get verified access, and each new expansion takes less bespoke effort than the last. Responsibilities Own the program for expanding access to Anthropic's life sciences verification programs: scoping, sequencing, dependencies, and tradeoffs across safeguards, platform, and product engineering teams Scope and drive the cross-org engineering work that each expansion requires, from new plan and account types to new platforms Partner with the product manager to turn program goals into a sequenced plan with clear owners and dates Drive clarity on data access, retention, and review re

What we're doing isn't easy. But nothing worth doing ever is. We envision a future powered by robots that work seamlessly with human teams. We build artificial intelligence that enables service robots to collaborate with people and adapt to dynamic human environments. Join our mission-driven, venture-backed team as we build out our customer-facing operations arm. As a Field Services Technician , you will be playing a critical role on the Field Services Team. Your work will directly impact clinical operations, ensuring the robotic fleet is well maintained and functional. You will work alongside onsite and engineering staff to execute preventative maintenance and incident triage. You will be the expert technician who is able to handle critical issues that few others can. This position requires a technician who is not afraid to roll up their sleeves and do what is necessary to keep our fleet operating at its maximum potential. We are looking for part-time, weekend coverage for this position and the starting hourly rate is $25/hr. . Your typical schedule will be: Friday: 4pm-9pm Saturday: 9am-5pm Sunday: 9am-5pm Job Responsibilities: Be willing and able to travel <80% of the time in order to support Robot service needs. Conduct routine and incident maintenance for our Robot Fleet. Provide support of Root Cause Analysis for major incidents in the Field. Provide timely repairs and decrease the time our Robots are out of production. Report on critical team metrics such as mean time to repair and first contact resolution rate. Required Experience and Qualifications: Local to Chicago, IL and able to travel within designated region (all expenses paid). <80% travel for site inspections and repairs escalated to engineering. Short-notice travel is required for this role. Read and understand manufacturing work instructions, mechanical assembly drawings and electrical schematics. Work with electrical and mechanical tools (digital multimeter, wire and pc

Locum Dissection Biomedical Scientist in Histology Banding: Band 6 Location: Derbyshire Start Date: ASAP Duration: Ongoing Working Pattern: Core hours only Hourly Rate: £30- £35 Band 7/8A We are currently seeking a Biomedical Scientist specialising in Dissection to join our client’s team in Derbyshire. This is a full-time, ongoing position working core hours only, offering a competitive hourly rate and the opportunity to contribute to a busy and well-established laboratory service. Key Responsibilities Will be responsible for undertaking various Dissection responsibilities within the Histology lab. You will be required to work across Cat B,C,D & E. Qualifications and Experience - HCPC registration - A Histology BMS with dissection experience no formal post grad qualifications, Histology BMS with the DEP in dissection undertaking Cat B & C, or a Histology BMS with the ASD in dissection undertaking Cat D & E - Experience in Histology within a clinical laboratory - Experience with microtomy and staining techniques - Strong attention to detail - Excellent communication and teamwork abilities - NHS experience (required) Why Work with Pulse? From the moment you register with Pulse, our focus is entirely on you. Our experienced recruitment consultants understand your specialty and are committed to finding roles that align with your skills and preferences. As a preferred or sole supplier to many clients, we offer exclusive opportunities not available elsewhere. We prioritise your professional goals, listen to your needs, and treat you as a valued individual—not just a resource. How to Apply If you are interested in registering with us, learning more about this position, or exploring other opportunities, we would love to hear from you. Please apply using the link below. Reasonable Adjustments If you have a disability or require any reasonable adjustments during the recruitment process or in the workplace, please let us know as early as possible. We are

Position Summary This is a full-time, contract hybrid position in South San Francisco, CA. The Contract Design Control Scientist supports the Platform department by owning and improving design controlled documentation across the product development lifecycle. This role bridges R&D science and regulatory compliance; translating laboratory processes, study data, and software workflows into traceable, audit-ready deliverables. The ideal candidate combines a strong scientific foundation with the ability to navigate regulated environments, engage cross-functional stakeholders, and communicate complex technical concepts to audiences ranging from R&D scientists to clinical professionals. Primary Responsibilities Author and maintain design controlled documentation in compliance with FDA QMSR, 21 CFR Part 11, GCP, CAP/CLIA, HIPAA, IVDR, and GDPR. Translate laboratory processes, study plans, and analytical data into traceable, compliant deliverables (e.g., development reports, verification/validation protocols, specifications). Establish and maintain traceability across project documentation, linking requirements to design outputs and verification evidence. Review development reports, team resources, and software scripts to extract and synthesize information for controlled documents. Create onboarding and training documentation for R&D and CLIA team members, including training plans and departmental practice descriptions. Manage documentation filing, version control, and change-control workflows within quality management systems. Identify opportunities to improve documentation processes, templates, and deliverable quality. Perform other duties as assigned. Qualifications BS or higher in a scientific discipline (molecular biology, biochemistry, genomics, or related field) or equivalent industry experience. 5+ years of experience producing controlled documentation in the medical device, IVD, or life science industry. Demonstrated experience working in