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The Clinical Doctor will assess patient suitability for weight management treatments and GLP-1 therapies through asynchronous consultations. They will also collaborate with multidisciplinary teams to improve clinical pathways and ensure safe, evidence-based patient care.
The Senior Clinical Pharmacologist will lead clinical pharmacology strategies across early and late-phase drug development programs while partnering with cross-functional teams to drive decision-making. They will apply model-informed drug development principles to support dose selection, biomarker optimization, and regulatory submissions.
The Research Nurse will coordinate and conduct clinical trial visits, ensuring all procedures and assessments are completed according to protocol and SOPs. They are responsible for maintaining accurate documentation, managing trial medication, and reporting adverse events to the project team.
The incumbent will lead medical science and strategy for metabolic clinical research, providing expert input on development plans, regulatory issues, and clinical trial protocols. They will also engage in business development, support client proposals, and mentor internal clinical teams to ensure high-quality delivery of research projects.
The incumbent will lead medical science and strategy for oncology, driving business outcomes through proposal development, client engagement, and strategic clinical trial design. They will also provide therapeutic expertise to internal teams, mentor clinical scientists, and contribute to innovative clinical research initiatives.
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The Senior Clinical Research Specialist manages end-to-end Investigator Sponsored Research (ISR) studies, including financial administration, contract negotiation, and regulatory compliance. They also lead process improvement initiatives and serve as a subject matter expert for clinical and purchasing systems within the Surgical Operating Unit.
The Clinical Doctor will assess patient suitability for weight management treatments and GLP-1 medications through asynchronous consultations. They will also collaborate with multidisciplinary teams to improve clinical pathways and maintain high standards of patient safety.
The Clinical Doctor will assess patient suitability for weight management treatments and prescribe medication safely through an asynchronous digital platform. They will also collaborate with multidisciplinary teams to improve clinical pathways and enhance the overall patient experience.
Serve as the primary medical and scientific strategic lead for psychiatry-focused clinical studies and business development. Collaborate with cross-functional teams to design protocols, execute study strategies, and provide expert medical input for internal and external stakeholders.
Provide general medical services across nursing homes, GP practices, and community clinics. Conduct remote consultations and maintain accurate patient documentation in accordance with clinical guidelines.
The Clinical Research Associate performs site qualification, initiation, monitoring, and close-out activities to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
The Medical Writer will transform complex clinical data into high-quality regulatory documentation, including clinical study reports and summary documents. They are responsible for ensuring all deliverables meet regulatory standards, internal quality requirements, and project timelines.
The Medical Writer will author, review, and edit clinical regulatory documents such as Clinical Study Reports and CTD summaries to meet regulatory standards. They will also contribute strategically to submission teams and collaborate with internal specialists to ensure high-quality, timely document delivery.
The supervisor will maintain clinical governance and risk management procedures while overseeing the daily operations of behavioral health coaches. They will collaborate with customer success teams to ensure service standards and best practices are met for digital mental health solutions.
Lead day-to-day clinical trial operations from start-up through close-out while managing study timelines and enrolment targets. Provide oversight of CRA activities, ensure protocol compliance, and manage relationships with sponsors and investigators.
The Clinical Project Leader will provide cross-functional leadership for clinical trials, ensuring projects are delivered on time, within budget, and in compliance with ICH GCP standards. They are responsible for managing client relationships, project P&L, and mitigating risks throughout the project lifecycle.
You will provide critical diagnostic information for veterinary patients while receiving mentorship and feedback from experienced radiologists. The role involves reading both known and live cases to prepare for board certification and maintain high reporting standards.
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The Medical Director oversees the execution of clinical trials in Neuroimmunology, specifically focusing on Lupus SLE, for a top-5 pharma client. Responsibilities include developing clinical development plans, overseeing medical writing for protocols, and managing clinical teams and scientific risks.
Manage the performance and workload of medical writers while overseeing the preparation and quality of publication deliverables. Lead resource planning, budget preparation, and the development of departmental training programs and SOPs.
Assess and manage patients seeking medical cannabis treatment for various women's health conditions, including endometriosis, PMDD, and menopause. Collaborate with a multidisciplinary team of nurses and pharmacists to provide high-quality care and contribute to clinical outcome data collection.
Assess and manage patients exploring cannabis-based medicines while making clinical decisions on treatment appropriateness. Collaborate with a multidisciplinary team of nurses and pharmacists to deliver high-quality psychiatric care and contribute to clinical outcome data collection.
Assess and manage patients exploring cannabis-based medicines while making clinical decisions on treatment appropriateness. Contribute to clinical outcome data collection and maintain robust standards of patient care within a multidisciplinary team.
The role involves serving as a statistical resource to mentor biostatisticians and oversee the preparation of Statistical Analysis Plans and clinical study reports. Additionally, the position focuses on maintaining R-based computing environments and developing Rshiny applications for data visualization.
Provide statistical support to the Medical Affairs group focusing on exploratory analysis, observational studies, and real-world evidence. Manage the statistical lifecycle of projects from protocol development to the final clinical study report.
Conduct 45-minute online psychological counseling sessions to help clients improve their mental well-being. Identify client needs and provide individualized, sustainable solutions for issues ranging from stress to career growth.
The specialist will plan, implement, and monitor the overall study supply chain strategy to maximize efficiency and minimize costs. This includes managing inventories of study drugs and collaborating with project management and vendors to optimize delivery processes.
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The Medical Director provides scientific input for core medical affairs activities, including strategy, HCP engagement, and evidence generation. They lead the Promotional Review Committee to ensure all materials are scientifically accurate and compliant.
Conduct high-quality, neuroaffirmative Autism and ADHD assessments for children and adults using virtual platforms. Provide evidence-based psychological therapy and collaborate with a multidisciplinary team to deliver person-centred care.
The specialist will triage and respond to drug information inquiries from healthcare professionals and patients while identifying and reporting adverse events. They will also perform medical writing tasks and coordinate processes for product quality complaints in compliance with regulatory standards.
This role involves managing direct reports, including coaching, training, and supporting staff development within the Medical Information Contact Center (MICC) team. The Associate Director will also ensure client success through oversight of assigned clients, managing deliverables, KPIs, and operational strategy.
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