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The role coordinates internal engagement, positioning, and advocacy efforts related to climate, environment, and health across the MSF movement. It involves facilitating the Intersectional Advocacy & Positioning Group and developing communication strategies to align stakeholders on complex climate dossiers.
The Clinical Specialist is responsible for reviewing clinical trial data and assessment scales to ensure standardized practices and data integrity. They provide guidance to raters through live discussions, feedback, and functional assessments like mock interviews.
Perform manual, independent reviews of clinical trial interviews and scale administrations to ensure scoring accuracy and protocol adherence. Senior roles involve clinical decision-making regarding site performance and overseeing targeted site interventions.
The Franchise Clinical Operations Development Lead is responsible for strategizing, planning, and executing the operational path for all indications within a franchise from first-in-human studies through commercialization. They also serve as a line manager for Clinical Operations Development Leads and act as a senior point of contact for clinical activities across the franchise.
The specialist will support the implementation and monitoring of the Banana Occupational Health and Safety Initiative (BOHESI) and contribute to the World Banana Forum's Working Group 3 on Labour Rights. Responsibilities include developing training materials, conducting research on labour policies, and coordinating field activities to promote decent work in global banana supply chains.
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The Medical Advisor acts as a hybrid medical affairs lead, connecting GSK to the healthcare community to advance clinical practice and respiratory therapeutic programs. They are responsible for executing medical strategic plans, engaging with key opinion leaders, and facilitating scientific exchange to address unmet medical needs.
The Medical Advisor will engage with healthcare providers to facilitate scientific exchange and advance clinical practice in respiratory therapeutics. They are responsible for executing medical strategic plans, collecting medical insights, and supporting clinical trials while ensuring compliance with company standards.
Conduct virtual wellness visits, health risk assessments, and medication reviews for patients in their homes. Collaborate with in-home clinical teams to coordinate care, manage referrals, and document patient findings.
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.
The Medical Science Liaison will engage in peer-to-peer scientific dialogue with healthcare professionals and serve as a key liaison between the company and clinical study sites. They will also provide scientific support for medical congresses, advisory boards, and internal teams to advance medical strategies.
The Associate Director will manage medical information activities for the EMEA region, ensuring accurate and timely responses to clinical inquiries from healthcare professionals and patients. They will also oversee the creation and maintenance of medical documentation while ensuring compliance with regulatory guidelines and internal SOPs.
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 Research Associate is responsible for conducting site visits, ensuring protocol compliance, and maintaining high-quality study documentation. They will also manage site relationships, support patient recruitment, and validate study data throughout the clinical trial lifecycle.
The Senior Manager will foster and maintain strategic relationships with electrophysiologists and key accounts across the EMEA region. They will act as a liaison between the organization and stakeholders to ensure consistent service, strategic engagement, and effective collaboration.
The Clinical Operations Development Lead co-leads the Clinical Development Team and is accountable for the strategic execution of clinical programs within agreed budgets and timelines. They oversee clinical trial activities, manage vendor relationships, and ensure compliance with regulatory standards throughout the compound lifecycle.
The Clinical Research Associate manages clinical site monitoring responsibilities, ensuring adherence to Good Clinical Practice and regulatory guidelines. They serve as the primary point of contact for sites, tracking study metrics and performing quality reviews of study documentation.
You will monitor and own the progress of clinical studies at investigative sites to ensure compliance with protocols, SOPs, and ICH-GCP regulations. Additionally, you will coordinate study setup activities, including identifying investigators and preparing regulatory submissions.
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You will monitor and own the progress of clinical studies at investigative sites to ensure compliance with protocols, SOPs, and ICH-GCP regulations. Additionally, you will coordinate study setup activities, including identifying investigators and preparing regulatory submissions.
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.
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.
Oversee and manage clinical trial activities to ensure adherence to protocols, regulatory requirements, and GCP standards. This includes conducting site visits, collaborating with cross-functional teams, and providing guidance to site staff to ensure data integrity and participant safety.
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.
Perform site monitoring visits including selection, initiation, and close-out while ensuring adherence to GCP and ICH guidelines. Manage study progress by tracking regulatory submissions, subject recruitment, and data query resolution.
Perform site monitoring visits including selection, initiation, and close-out while ensuring adherence to GCP and ICH guidelines. Manage study progress by tracking regulatory submissions, subject recruitment, and data query resolution.
The Quality Manager is responsible for developing and maintaining the Quality Management System (QMS) in alignment with international standards like GCP and ISO. Key duties include managing audits, CAPA processes, risk assessments, and ensuring regulatory compliance across the clinical area.
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Oversee and manage clinical trial activities to ensure adherence to protocols, regulatory requirements, and industry standards. Lead monitoring tasks, conduct site visits, and collaborate with cross-functional teams to ensure accurate data collection.
Support clinical trial procedures and patient enrollment for Electrophysiology therapies across Europe. Act as a technical expert to train clinical staff and collaborate with cross-functional teams to optimize study design and execution.
Provide medical leadership and oversight for ophthalmology clinical programs across all development phases, including medical monitoring and safety review. Act as a primary client-facing representative to support business development and shape clinical strategies for proposals.
Remotely administer semi-structured clinical interviews and cognitive assessment batteries to study subjects and caregivers. Provide central monitoring by reviewing neuropsychological test batteries to ensure accuracy in administration and scoring.
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