Clinical Specialist Joint Replacement Jobs

Truveta is the world's first health provider-led data platform with a vision of Saving Lives with Data . We empower researchers, clinicians, and healthcare organizations through high-quality clinical data and AI-driven insights. We are seeking an experienced clinical professional to manage a team of Clinical Terminologists, Data Annotators, and Clinical Abstractors responsible for clinical terminology mapping, data annotation, and data quality. The ideal candidate is a self-starter who excels at developing high-performing teams, driving operational excellence, and delivering projects with exceptional quality and timeliness. Work Location: Hyderabad, India This Opportunity Join the founding team of the Truveta India Development Center (IDC) and play a pivotal role in shaping its future. As one of the initial members, you'll help build and scale a high-impact organization while contributing to products and platforms that advance healthcare through data and AI. This is a unique opportunity to influence both the technical direction and the culture of a growing global engineering hub. Key Responsibilities Lead, mentor, and develop a team of Clinical Terminologists, Data Annotators, and/or Clinical Abstractors by providing coaching, training, and performance guidance. Oversee terminology mapping and clinical data normalization using standards such as SNOMED CT, RxNorm, and LOINC , ensuring exceptional quality and consistency. Drive project execution by managing priorities, monitoring team performance, and ensuring deliverables are completed on time with minimal oversight. Collaborate cross-functionally with Engineering, Product, Program Management, and AI/ML teams to improve clinical data pipelines and annotation processes. Establish and continuously improve quality standards, workflows, documentation, and operational processes to support scalable clinical data operations. Key Qualifications MBBS

We are seeking a dedicated Clinical Research Physician to join our team in the North West. The ideal candidate will be involved in conducting clinical trials, ensuring they meet regulatory standards while advancing medical knowledge. This role is flexible, offering both part-time and full-time opportunities. Responsibilities: Conduct and oversee clinical trials in compliance with regulatory requirements. Ensure patient safety and adherence to study protocols. Collaborate with research teams to analyze and interpret clinical data. Prepare and review clinical trial documentation and reports. Maintain up-to-date knowledge of clinical research advancements and regulations. Communicate effectively with stakeholders, including patients, sponsors, and regulatory bodies. Qualifications: Minimum of 1 year of clinical research experience. Good Clinical Practice (GCP) certification is preferred. Advanced Life Support (ALS) or Immediate Life Support (ILS) certification is preferred. Medical degree with a valid medical license. Strong analytical and problem-solving skills. Excellent communication and organizational abilities.

We are seeking a dedicated Clinical Research Physician to join our team in Manchester, either on an ad hoc or full-time basis. This role involves overseeing clinical trials, ensuring patient safety, and maintaining regulatory compliance, contributing to groundbreaking research and advancements in healthcare. The areas are Leigh, Manchester and the Wirral, Responsibilities: Oversee the planning, execution, and management of clinical trials. Ensure adherence to clinical trial protocols and regulatory guidelines. Monitor patient safety throughout research studies. Collaborate with cross-functional teams to ensure successful trial outcomes. Provide leadership and mentorship to junior research staff. Stay updated with the latest developments in clinical research and trial methodologies. Qualifications: Medical Degree with full GMC registration and a license to practice. 1-3 years of experience in clinical trials or research, with exposure to leadership or mentorship roles. Strong understanding of clinical trial operations, patient safety, regulatory compliance, and protocol adherence. Familiarity with ICH-GCP guidelines and ethical standards in clinical research. · Familiarity with ICH-GCP guidelines and ethical standards in clinical research.

Clinical Database Programmers are operationally responsible to provide technical support and oversight for the Medidata Clinical Cloud (MCC) implementation activities. Clinical Database Programmers will maintain project level perspective, focus and communicate effectively as the MCC SME on technical and functional electronic data capture programming and data management activities, timelines and deliverables. KEY TASKS & RESPONSIBILITIES Design/develop and test clinical databases including forms, folders, matrices, data dictionaries, unit dictionaries, edit checks, derivations, custom functions, standard and custom reports Performs peer review for the studies built by other Clinical Database Programmers Responsible for the development, maintenance, and compliance of database builds and EDC standards in support of clinical studies including, but not limited to, Global Library, Edit Checks, CRF modules Manages timely-quality deliverables for the study teams for assigned protocol/study(s) Functions as an EDC Subject Matter Expert (SME) providing guidance and best practice recommendations to Data Management, operations teams, and other stakeholders on basic Medidata Rave functionality Working knowledge of additional Medidata Rave modules, including Coder, RTSM, Lab Admin, iMedidata/Cloud Admin or other modules. Other duties as assigned CANDIDATE’S PROFILE Education & Experience Bachelor’s degree or equivalent work experience preferred 2+ years in Pharmaceutical/Biotechnology industry or equivalent preferred Experience with requirements gathering, design and specification development of CRFs, edit checks, site queries, and understanding of database structures and programming languages Professional Skills Ability to work creatively and independently to carry out assignments of a complex nature Ability to communicate and work effectively and cooperatively with other professional staff members Detail oriented, ability to multitask with str

Opportunity Overview: The Clinical Review & Correspondence RN plays a critical role in supporting utilization management operations by conducting medical necessity reviews, preparing clear and compliant clinical determinations, and ensuring accurate member and provider communications. In collaboration with Medical Directors and cross-functional partners, this role ensures that clinical decisions are evidence-based, align with regulatory and accreditation standards, and are communicated effectively and timely. Through precise clinical review and documentation, you will help support high-quality care, regulatory compliance, and improved member outcomes. What you’ll do: Consult with Medical Directors on clinical determinations, medical necessity decisions, and related clinical correspondence Prepare clear, accurate, and compliant member and provider communications in alignment with regulatory and organizational requirements Understand regulatory requirements governing utilization management decisions and ensure appropriate application to clinical determinations and communications Understand when and why member and provider notifications are required, including regulatory and clinical triggers for written communication Support verbal notification workflows when timely communication of clinical determinations is required Document clinical information completely, accurately, and in a timely manner Consistently meet or exceed productivity, quality, and turnaround time expectations Maintain a thorough understanding of accreditation and regulatory requirements and ensure utilization management decision-making and timeliness standards remain in compliance Perform other duties as assigned What you’ll need: Registered Nurse with active, unencumbered license in the state of residence Experience developing member and provider correspondence within a health plan environment Minimum of 3 years of clinical experience Utilization Management experience required Knowledge of

Truveta is the world’s first health provider led data platform with a vision of Saving Lives with Data. Our mission is to enable researchers to find cures faster, empower every clinician to be an expert, and help families make the most informed decisions about their care. Achieving Truveta’ s ambitious vision requires an incredible team of talented and inspired people with a special combination of health, software and big data experience who share our company values. Truveta was born in the Pacific Northwest in the USA and has employees who live across the country. As we expand our global footprint with a new presence in Hyderabad, India, we’re building a world-class team to help us scale this mission and Clinical Intelligence and AI Evaluation is at the heart of everything we do. This job requires daily onsite work at our headquarters in Hyderabad, India. Who We Need Truveta is rapidly building a talented and diverse team to tackle complex health and technical challenges. Beyond core capabilities, we are seeking problem solvers, passionate and collaborative teammates, and those willing to roll up their sleeves while making a difference. If you are interested in the opportunity to pursue purposeful work, join a mission-driven team, and build a rewarding career while having fun, Truveta may be the perfect fit for you. This Opportunity At Truveta, we believe that high data quality will play a critical role in accomplishing our mission towards saving lives with data. An important component of this work is data normalization in which the medical terminology linking, and terminology management are essential in building deep intelligence empowering the new generation of clinical research. We are looking for a full-time Clinical Terminologist who will help to standardize the data sourced from different health systems. The responsibilities include identifying, creating, or validating mapping between medical terms from various healthcare system to standardized Terminologies

Axsome Therapeutics is a biopharmaceutical company leading a new era in the treatment of central nervous system (CNS) conditions. We deliver scientific breakthroughs by identifying critical gaps in care and develop differentiated products with a focus on novel mechanisms of action that enable meaningful advancements in patient outcomes. Our industry-leading neuroscience portfolio includes FDA-approved treatments for major depressive disorder, agitation associated with dementia due to Alzheimer’s disease, excessive daytime sleepiness associated with narcolepsy and obstructive sleep apnea, and migraine, as well as multiple novel product candidates addressing a broad range of serious neurological and psychiatric conditions that impact over 150 million people in the United States. Together, we are on a mission to solve some of the brain’s biggest problems so patients and their loved ones can flourish. For more information, please visit us at www.axsome.com and follow us on LinkedIn and X . About This Role: Axsome Therapeutics is seeking a Clinical Trial Manager/Senior Clinical Trial Manager who will be the primary operational lead for a study and will lead the cross-functional team for execution of the study. The Clinical Trial Manager/Senior Clinical Trial Manager provides operational leadership to the study team to ensure project milestones deliver on time, within budget, high quality, and in compliance with the ICH / GCP, regulatory authority’s regulations/guidelines, and applicable SOPs. This position will manage essential duties and responsibilities as independently as possible, with guidance and oversight provided by the program director when needed. This role is based at Axsome’s HQ in New York City with an on-site requirement of at least three days per week. We are unable to consider candidates who are looking for fully remote roles. Job R

Job Title Clinical Psychologist – Neurodevelopmental Assessments (ADOS-2 & ADI-R) Banding Any Banding Location Face-to-face ADOS-2 assessments in Macclesfield, remote ADI-r assessments. Working Hours Flexible – choose your own hours. Hybrid working available. Salary Headline PAYE rates: ADI-R (Remote): £380 ADOS-2 (Face-to-Face): £225 Join a Growing Service We are seeking Clinical Psychologists to deliver autism diagnostic assessments, including ADOS-2 and ADI-R . This is an exciting opportunity to join a new and expanding service , where you can get in at the ground floor and help shape its future. Enjoy the flexibility of hybrid working, with remote ADI-R interviews and face-to-face ADOS-2 assessments. The service is open to flexible scheduling, so you can pick your own hours . Responsibilities Conduct both ADOS-2 and ADI-R assessments for autism diagnosis. Deliver ADI-R remotely and ADOS-2 face-to-face. Collaborate with another clinician during ADOS assessments. Ensure accurate, high-quality reporting and contribute to a positive client experience. Benefits Flexible working – choose your own hours. Hybrid model – remote and face-to-face work. Opportunity to shape and grow a new service . Competitive PAYE rates. Supportive team environment. Qualifications & Experience HCPC registered Clinical Psychologist. Experience conducting ADOS-2 and ADI-R assessments (essential). Strong communication and report-writing skills. Applicants who do not meet all requirements are still encouraged to apply! How to Apply Apply via the Pulse website today. Our recruitment team will contact you to discuss the role and next steps. Why Work With Pulse Pulse offers dedicated support, competitive rates, and access to a wide range of roles tailored to your expertise. Reasonable Adjustments We are committed to supporting applicants with reasonable adjustments throughout the recruitment process.

Clinical / Forensic Psychologist – Wiltshire Salary: £60,000 per annum | Hours: Full-time (37.5 hrs) | Hybrid Working We are seeking a passionate Clinical or Forensic Psychologist to deliver a comprehensive therapeutic service for children in care across Wiltshire. This is an exciting opportunity to work with four new children’s homes, including an assessment home, supporting young people who have experienced trauma and complex challenges. What we offer: Competitive salary and hybrid working Career progression through our Education Academy Extensive CPD and therapeutic training Wellbeing benefits including Blue Light Card, Taste Card, and Employee Assistance Programme What we’re looking for: HCPC-registered Clinical or Forensic Psychologist Experience working with children and young people with complex needs Strong skills in assessment, safeguarding, and evidence-based interventions Full UK driving licence and access to a car

Clinical Vendor Oversight Senior Informaticist — Louisville, KY. Apply via Workday.

Clinical Research Associate I — United States - California - Alameda. Apply via Workday.

Clinical Product - Senior Manager — AZ - Work from home. Apply via Workday.

Lead Technician, CIC (Clinical Intervention Center) — SC - Work from home. Apply via Workday.

Premier·ère adjoint·e de recherche clinique I // Senior Clinical Research Associate I — 5 Locations. Apply via Workday.

Director, Clinical Development Scientist (Non-MD) — 6 Locations. Apply via Workday.