Clinical Review Rn Jobs

Opportunity Overview: We are seeking a Financial Analyst to join our FP&A team. This is a hands-on, detail-oriented role embedded within our Commercial organization. The right candidate brings sharp analytical instincts, a bias for action, and the ability to deliver reliable financial support at a pace that keeps up with a fast-moving sales team and pricing leader What you’ll do: Develop, maintain, and utilize pricing models to forecast profitability, revenue impact, and margin changes Analyze the cost impact of process and product improvements, incorporating them into financial and pricing models Partner with Commercial, Clinical/Operations, and Actuarial teams to develop comprehensive pricing models and present strategic summaries to executive leadership Review and approve deal opportunities, RFP responses, custom pricing structures, and discounting frameworks Gather and compile data points from internal systems to monitor financial performance, metrics, and client profiles Assist with organization-wide strategic projects and provide scenario modeling, serving as the subject matter expert for pricing strategy and inputs Support budget and forecast preparation for the sales and marketing organizations — partnering with the team to build credible, data-backed plans Utilize Adaptive Insights (Workday Adaptive Planning) to manage planning cycles, scenario modeling, and financial reporting with efficiency and accuracy Apply AI-powered analytics tools to automate routine tasks, surface insights faster, and continuously elevate the quality of financial outputs ISMS roles and responsibilities Fair understanding of Information Security practices. Align to the organization policies and procedures. Ensure to get updated with ISMS roles as assigned by the department/process heads. Required Qualifications: Must-haves 3–6 years of pricing, commercial finance, or operations finance experience; healthcare, BPO, or technology-enabled services industry background preferred Adva

Job Title: Lead - Aggregate Reporting Employment Type: Full-time Work Type: Remote About ClinChoice: ClinChoice is a partner to the largest pharmaceutical, medical device, and consumer care innovators in the world. Established in 1995, we provide expertise in clinical operations, biometrics, regulatory affairs, pharmacovigilance, medical affairs, and toxicology to help our partners advance healthcare by accelerating clinical trials with data-driven insights, delivering the best strategies for product registration, and enhancing patient safety through real-world and clinical analysis. Our global delivery network has expanded to centers and satellite offices in the United States, Mexico, the United Kingdom, Armenia, China, Japan, India, and the Philippines to help our customers maintain regulatory compliance locally and globally. We have forged future-defining partnerships with industry bodies and technology companies to develop cutting-edge solutions that deliver our expertise with quality and precision. Primary Responsibilities: Responsible for authoring Aggregate Safety Reports (including but not limited to PBRER/PSUR, ACO, DSUR, PADER, CAR, RMP, Ad-hoc safety reports for medicinal and non-medicinal products and EU-MDR PSUR, PMSR, PMSP, and PRER reports for medical devices, and Cosmetovigilance reports for Cosmetic products for submissions to various health authorities as per the requirement). Plan report-specific timelines, identify relevant stakeholders, request calls for contributions, and coordinate with various stakeholders for obtaining relevant data for the preparation of aggregate safety reports. Review the safety data (including the seriousness and expectedness assessments of events, as may be necessary) as per the agreed strategy and sponsor’s conventions and verify the correctness and completeness of contributions received from stakeholders. Perform aggregate review of post-marketing cases received in global databases and assess whether the cases alter t

Opportunity Overview: We are seeking a Lead Data Engineer to drive the design and delivery of our cloud-native healthcare data platform. You will lead the implementation of scalable data solutions built on AWS, Apache Iceberg, Lake Formation, Glue Catalog, Athena, dbt, and modern orchestration frameworks. This role combines deep hands-on engineering with technical leadership and collaboration across platform, analytics, and business teams. What you’ll do: Lead Data Engineering Initiatives Lead delivery of complex data engineering projects across multiple teams Drive technical execution from design through production deployment Establish scalable implementation patterns Build and Optimize Data Platforms Design and implement batch and near-real-time pipelines Build reusable ingestion, transformation, validation, and publishing frameworks Support modernization of legacy workloads Lakehouse Engineering Lead Apache Iceberg implementation and optimization Define standards for schema evolution, partitioning, compaction, and metadata management Ensure efficient storage and query performance Data Quality and Reliability Implement data quality frameworks Drive observability and monitoring practices Improve operational excellence and reliability Technical Leadership Review architecture and design proposals Conduct code reviews and engineering reviews Mentor engineers and establish best practices ISMS roles and responsibilities: Good knowledge of Information practices. Assist the manager in all the information security activities implementation and maintenance process. Ensuring the team and imparted with Competence related to Information security Responsible for implementation of security policies and procedures and report any issues to the Information Security Manager. Required Qualifications: 8–12 years of Data Engineering experience. Experience leading enterprise-scale data initia

Responsibilities: Annotate Case Report Form (acrf.pdf) following FDA/CDISC or sponsor guidelines. Develop SDTM specifications and generate SDTM datasets using SAS; Develop ADaM,specifications and generate ADaM datasets using SAS based on Statistical Analysis Plan; Develop Tables, Listings, Graphs, Patient Profile in support of the Clinical Study Report, Posters, Manuscripts; Develop ADaM data, Tables, Listings, Figures for Integrated Summary of Safety (ISS) and Integrated Summary of Efficacy (ISE) Create electronic submission packages to FDA, e.g., define.xml or define.pdf following FDA guidelines with no supervision. Expert-level in analyze information and develop innovative solutions to programming and data analysis challenges; Serve as point of contact (POC) of programming with statisticians for statistical input and analysis interpretation; Follow and reinforce regulatory agency requirements during daily job. Serve as a programming team lead and contribute to department initiatives. Provide guidance, mentoring, training for team members and help solve issues from cross-functional teams; Review draft and final production deliverables for project to ensure quality and consistency. Work with global team or sponsors to coordinate project deliverables, timelines and resources. Skills and Responsibilities: Bachelor’s/Master’s degree in Statistics, Mathematics, Computer Science, Electrical Engineering, Biotechnology or related scientific disciplines with 5+years of clinical programming experience. Proven knowledge and training in high level computing languages such as. SAS, C/C++, Java, R, Python, MATLAB and SQL. Database programming experience is a plus. Expert-level in decoding programming logic and assembling programming code based on logic provided and be able to explain to team members. Expert level in applying concept in Artificial Intelligence and Machine Learning in real world. In-depth knowledge of ICH, Good Clinical Practices, Clinical research, Clinical tria

Job Title: Band 7 Pharmacist Band: Band 7 Location: East London Department: Pharmacy Specialty: Mental Health Pharmacy Start Date: ASAP, 3 months with opportunity to extend Pay Rate: Competitive Job Overview Pulse is seeking a skilled and motivated Band 7 Pharmacist to join a specialist mental health pharmacy team in East London. This role offers an excellent opportunity to provide high-quality clinical pharmacy services, supporting medicines optimisation and improving patient outcomes within a multidisciplinary healthcare setting. Key Responsibilities Clinically screen prescriptions to ensure safe, effective, and appropriate prescribing. Perform medicines reconciliation for patients admitted to and discharged from services. Provide patient counselling and education relating to prescribed treatments. Respond to medicines-related enquiries from patients, carers, and healthcare professionals. Support medicines optimisation initiatives and promote best practice in medication management. Provide specialist pharmaceutical advice to multidisciplinary teams. Monitor and review medication regimens to improve patient outcomes. Maintain accurate clinical records and documentation in accordance with local policies. Contribute to service development, audit, and quality improvement activities. Qualifications and Experience Registered Pharmacist with the General Pharmaceutical Council (GPhC). Previous hospital pharmacy experience is essential. Experience working within mental health services is highly desirable. Clinical Pharmacy Certificate, Diploma, or equivalent postgraduate qualification in mental or physical health. Strong understanding of clinical pharmacy practice and medicines optimisation. Excellent communication and interpersonal skills. Ability to work effectively as part of a multidisciplinary healthcare team. Commitment to delivering high-quality patient-centred care. Why Choose Pulse? Competitive pay rates. Dedicated specialist pharmacy recruitment consultant. Acces

Job Title: Clinical Pharmacist Banding: Band 8 Location: Northwest London Start Date: 1st October 2026 Duration: Until 31st October 2026 Hourly Rate: Competitive Working Hours: Monday to Friday, 09:00 to 17:00/17:30 (7.5 hours per day, Full-Time) Job Overview Pulse is currently seeking an experienced and motivated Band 8 Clinical Pharmacist to join the pharmacy team in Northwest London. This is an excellent opportunity to work within one of the UK's leading private healthcare hospitals, providing specialist clinical pharmacy services and supporting the safe, effective, and patient-centred use of medicines. The successful candidate will work closely with multidisciplinary teams to deliver high-quality pharmaceutical care, support medicines optimisation, and ensure the highest standards of clinical practice across inpatient services. Key Responsibilities Provide specialist clinical pharmacy services across designated wards and clinical areas. Review prescriptions and support the safe and effective use of medicines. Undertake clinical medication reviews and medicines reconciliation activities. Provide expert pharmaceutical advice to consultants, nursing staff, and other healthcare professionals. Support medicines optimisation initiatives to improve patient outcomes. Contribute to safe discharge planning and continuity of care. Participate in clinical governance, audit, and service improvement activities. Maintain accurate documentation in accordance with professional and regulatory standards. Qualifications and Experience Be registered with the General Pharmaceutical Council (GPhC). Have substantial hospital pharmacy experience. Demonstrate experience working at Band 8 level or equivalent. Possess strong clinical knowledge across a broad range of therapeutic areas. Be confident working independently and within multidisciplinary teams. Have excellent communication, organisational, and clinical decision-making skills. Experience within a private healthcare setting is des

Job Title: Clinical Anticoagulation Pharmacist Banding: Band 7 Location: Chertsey Surrey Start Date: ASAP Duration: Ongoing Hourly Rate: £30 - £32 Working Hours: Monday to Friday, Full-Time Job Overview Pulse is currently seeking an experienced and motivated Band 7 Clinical Anticoagulation Pharmacist to provide specialist locum support to the pharmacy team in Chertsey Surrey. This is an excellent opportunity for a clinical pharmacist with experience in anticoagulation services to play a key role in delivering safe, effective, and patient-centred care within a busy NHS hospital setting. The successful candidate will work closely with multidisciplinary teams to optimise anticoagulation therapy, support medicines management initiatives, and ensure patients receive the highest standard of pharmaceutical care. Key Responsibilities Provide specialist clinical pharmacy support for anticoagulation services. Review and optimise anticoagulation therapy to ensure safe and effective patient care. Provide expert pharmaceutical advice to medical, nursing, and allied healthcare professionals. Undertake clinical medication reviews and medicines reconciliation activities. Monitor patients receiving anticoagulant therapy and support dose adjustments where appropriate. Contribute to the development and implementation of anticoagulation-related guidelines and protocols. Support patient education and counselling regarding anticoagulant medicines. Participate in audit, governance, and quality improvement initiatives relating to anticoagulation services. Qualifications and Experience Be registered with the General Pharmaceutical Council (GPhC). Have previous NHS hospital pharmacy experience at Band 7 level or equivalent. Demonstrate experience working within anticoagulation services or managing anticoagulant therapies. Possess strong clinical knowledge of anticoagulant medicines and associated monitoring requirements. Be confident working independently and within multidisciplinary teams.

Job Title: Clinical Pharmacist Banding: Band 7 / 8a Location: Croydon, London Start Date: ASAP Duration: 6 Months (option to extend) Hourly Rate: £31-36 Working Hours: Full-time Job Overview Pulse is currently seeking two experienced Clinical Pharmacists (Band 7 / Band 8a) to join a busy acute hospital team in Croydon. This is an excellent opportunity for hospital pharmacists with strong ward-based experience to contribute to the delivery of safe, effective, and patient-centred pharmaceutical care within a dynamic NHS environment. The successful candidates will provide clinical pharmacy services across hospital wards, supporting medicines optimisation and ensuring the safe prescribing and use of medicines throughout the patient journey. Key Responsibilities Undertake comprehensive medication histories and medicines reconciliation on admission Provide ward-based clinical pharmacy services as part of the multidisciplinary team Conduct clinical screening of inpatient prescriptions and medication charts Review and screen TTAs (To Take Away medications) prior to discharge Identify, resolve, and prevent medication-related issues to optimise patient outcomes Support medicines optimisation initiatives and clinical governance activities Provide expert pharmaceutical advice to medical, nursing, and allied health professionals Ensure compliance with Trust policies, national guidelines, and medicines legislation Utilise Electronic Prescribing and Medicines Administration (EPMA) systems effectively within daily practice Qualifications and Experience Registered Pharmacist with the General Pharmaceutical Council (GPhC) Previous NHS hospital pharmacy experience is essential Significant experience working in a ward-based clinical pharmacy role Proven experience undertaking: Drug histories Medicines reconciliation Clinical screening TTA screening Experience using EPMA systems is essential Experience with Cerner EPMA is highly desirable Excellent clinical knowledg

eClinical Solutions is a global leader in clinical data intelligence, delivering the elluminate® Clinical Data Cloud® — an AI-powered platform driving agentic data review, SDTM automation, and RBQM for 18 of the top 50 pharmaceutical companies worldwide. As part of our eNOVA AI-First transformation, we are embedding AI across every pillar of clinical development and enterprise operations — compressing cycle times, improving data quality, and redefining how work gets done. As we scale our AI capabilities, we are building a high-impact, hands-on AI engineering function focused on delivering real, production-grade automation across the enterprise. You will make an impact: The Principal AI Engineer – Automation & AI is a hands-on technical leader responsible for designing, building, and deploying AI-powered automation solutions across eClinical Solutions. This role is builder-first (70–80% hands-on development) and operates within a small, high-output team (2–4 engineers). You will work directly with the CTAO and business leaders to identify high-value use cases and rapidly translate them into working AI systems in production. This is not a program management or oversight role. You are expected to build, ship, and iterate continuously, leveraging modern AI tooling and agentic frameworks to deliver measurable impact. Accelerate your skills and career within a fast-growing company while impacting the future of healthcare. Your day to day: Building & Shipping AI Systems Design and deploy agentic AI workflows and automation solutions across enterprise functions including R&D, Engineering, Professional Services, IT, Finance, Sales, and Marketing Build production-grade systems such as: Multi-agent workflows RAG-based applications Document intelligence and summarization pipelines Workflow and process automation solutions Use modern AI tools and frameworks including: Codex, Claude Code, Gemini, NotebookLM LangChain, LangGraph, LlamaIndex (or equivalent

Job Title: Band 7 Pharmacist Banding: Band 7 Location: Bristol Start Date: ASAP Duration: 3 months with option to extend Hourly Rate: £30 - £31 Working Hours: Monday to Friday, 08:45 – 17:15 Job Overview Pulse is currently seeking an experienced and motivated Band 7 Pharmacist to join the pharmacy team in Bristol. This is an excellent opportunity for a skilled clinical pharmacist to provide high-quality pharmaceutical care within a busy hospital environment, supporting the pharmacy service during a period of maternity leave cover. The successful candidate will work closely with multidisciplinary teams to optimise medicines management, support safe prescribing practices, and contribute to the delivery of patient-centred care across a range of clinical specialties. Key Responsibilities Provide clinical pharmacy services to designated wards and departments. Review prescriptions and deliver expert advice on medicines optimisation. Support the safe, effective, and cost-efficient use of medicines. Undertake medicines reconciliation and contribute to discharge planning processes. Work collaboratively with medical, nursing, and allied healthcare professionals. Participate in clinical audits, service improvement initiatives, and governance activities. Maintain accurate patient records and comply with professional and regulatory standards. Qualifications and Experience Be registered with the General Pharmaceutical Council (GPhC). Have previous hospital pharmacy experience. Hold a Postgraduate Certificate or Diploma in Clinical Pharmacy, or equivalent experience. Demonstrate strong clinical knowledge and decision-making skills. Be confident working independently and as part of a multidisciplinary team. Possess excellent communication, organisational, and problem-solving abilities. Have experience delivering patient-focused clinical pharmacy services within a hospital setting. Why Choose Pulse? From the moment you register with Pulse, our focus is en

Job Title Clinical/Forensic Psychologist Banding Band 8a/b Location Grimsby (covering North East Lincolnshire and North Lincolnshire) Working Hours Up to 30 hours per week - locum contract Salary Competitive, DOE - opportunity for higher salaries Opening Paragraph Pulse is seeking an experienced Clinical/Forensic Psychologist to join a Learning Disabilities service in Grimsby. This is a unique opportunity to work within a psychology-led, multi-disciplinary team supporting individuals with learning disabilities and/or autism who are at risk of offending or have an offending history. You’ll play a key role in helping service users transition safely from secure care into the community, reducing risk and promoting independence. The role offers competitive pay, flexible working hours, and the chance to make a real impact in a specialist forensic setting. Responsibilities In this role, you will: Lead the delivery of highly specialist psychological assessments and interventions. Provide clinical supervision and consultation to colleagues and partner agencies. Take a senior role in managing complex cases and risk assessments. Deliver offence-specific therapeutic interventions and treatments. Chair and facilitate complex case reviews and multi-agency meetings. Contribute to service development, policy review, and research initiatives. Communicate complex psychological formulations and treatment plans effectively within the multidisciplinary team. Benefits Competitive salary and NHS pension scheme. Flexible working arrangements. Opportunities for professional development and CPD. Work within a supportive, psychology-led team. Access to specialist forensic services and multi-agency collaboration. Make a meaningful difference in transforming care for vulnerable individuals. Qualifications and Experience Essential: Doctoral-level training in Clinical or Forensic Psychology (BPS accredited). Current HCPC registration. Experience working with complex cases and challenging beh

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 122,000 colleagues serve people in more than 160 countries. JOB DESCRIPTION: Position Overview The Product Development and Automation Senior Scientist provides services of a technical nature to support the development, implementation, and maintenance of automation, IT, and software systems used in the clinical laboratory. The Product Development and Automation Senior Scientist will perform moderate and highly complex analytical processes to support feasibility and validation studies. This includes wet lab testing for feasibility, verification and validation of lab automation, workflow, and software. This role will also be responsible for performing user acceptance testing (UAT), and validation of Laboratory information system (LIS) system changes and upgrades. This role will collaborate with end users and LIS developers to address needed improvements to current modules, design requirements for new test systems, validation, and implementation of the changes. Once resources are identified, can get a project off the ground and running with minimal support from management. Can make new processes, systems, validation methods or projects successful. Essential Duties Include, but are not limited to, the following: Assist in UAT testing Edit and review controlled documents within the laboratory document control system to support changes or implementation of software and process changes. Contributes ideas and insights to new technologies, testing methodologies, applications, techniques or procedures that are creative and practical. Provides input

eClinical Solutions helps life sciences organizations around the world accelerate clinical development initiatives with expert data services and the elluminate Clinical Data Cloud – the foundation of digital trials. Together, the elluminate platform and digital data services give clients self-service access to all their data from one centralized location plus advanced analytics that help them make smarter, faster business decisions. OVERVIEW Quality Control Specialists are operationally responsible for performing quality control activities associated with Biometrics client’s deliverables. Quality Control Specialists will maintain project level perspective, focus, and communicate effectively as the quality control subject matter expert. KEY TASKS & RESPONSIBILITIES Perform quality control activities (i.e. documentation review, testing) of Biometrics client’s Rave EDC and Data management deliverables including eCRFs, Data Validation Specification checks, Custom functions, Data Extracts, Data Integrations, Data Mapping, Custom Data Management Reports and listings Participate in the design and development of quality control procedures Manage documentation created during the QC process Liaise with study teams and other staff to fulfill job responsibilities and activities Develop and lead execution of training and knowledge transfer opportunities for quality control team Inform the Manager of training issues, project activities, quality issues and timelines as directed Collaborate with the project team to ensure the deliverables are completed on time with high quality Other duties as assigned CANDIDATE’S PROFILE Education/Language: Four-year college degree or higher preferred, analytic discipline a plus (Computer Science or Health related field) Excellent knowledge of English Professional Skills & Experience Minimum 3-5 years in Pharmaceutical/Biotechnology industry or equivalent Knowledge of ICH/GCP guidelines, 21 CFR Part 11, cli

At Kailera, we are bold, authentic and committed to our mission of developing therapies that give people the power to transform their lives and elevate their overall health. Rooted in an entrepreneurial spirit and a team-oriented culture, we are working together to advance Kailera’s mission to advance novel therapies for obesity and related conditions. We are passionate about creating an inclusive workplace that promotes collaboration, integrity, and excellence. As we expand, we seek the most talented individuals with diverse backgrounds, cultures, perspectives, and experiences to join our team. What You’ll Do: We are seeking an experienced programmer to join us as Associate Director, Statistical Programming. This is a critical role responsible for leading statistical programming activities on the assigned disease area(s). This role will support clinical trials, regulatory submissions, and other key initiatives. Required location: Waltham, MA (hub-based, onsite 3-4 days per week) OR Remote (home-based, onsite at a hub 1 week every other month). Responsibilities: Lead statistical programming efforts for clinical studies, including the development and review of programming specifications to ensure clarity, integrity, and compliance with internal and external standards Lead the execution of ad-hoc and post-hoc analyses to support emerging clinical questions, publications, and internal decision-making Oversee and coordinate activities with Contract Research Organizations (CROs), focusing on the implementation of CDISC standards, creation of SDTM, ADaM datasets, and TFLs, and ensuring high-quality deliverables Conduct independent validation and quality checks of statistical programming deliverables from CROs Collaborate closely with statisticians and cross-functional study teams to deliver results in a timely and accurate manner Manage multiple projects simultaneously, ensuring tasks are prioritized effectively to meet deadlines Required Quali

Start: ASAP Hours: 2–3 days per week Duration: 3 months (review after) Location: Multiple sites (South) Remote: Partly Client Group: Adults with Autism Role Overview We’re seeking an experienced Psychologist to oversee five social care residences and supervise two Assistant Psychologists . You’ll provide specialist psychological services for adults with ASD and learning disabilities, including assessments, formulations, interventions, and risk management. The role involves working across multiple sites and liaising with multidisciplinary teams. Key Responsibilities Deliver psychological assessments and evidence-based interventions. Formulate treatment plans and manage complex cases. Conduct risk assessments and contribute to risk management. Provide specialist advice, consultation, and clinical supervision. Liaise with staff across services to ensure coordinated care