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The Principal Biostatistician leads biomarker-related statistical activities across clinical studies, serving as the primary contact for sponsors. They are responsible for developing biomarker evaluation plans, conducting advanced data analysis, and mentoring junior staff to ensure high-quality deliverables.
The Principal Biostatistician leads statistical activities across multiple studies, serving as the primary sponsor contact and providing expert consultancy on study design and protocol development. They also oversee project deliverables, mentor junior staff, and ensure compliance with regulatory standards throughout the clinical trial lifecycle.
The Clinical Success Manager will demo, install, and train clinics on automation software while proactively managing customer relationships and feedback. They will also collaborate with the sales team to support prospective customers and develop training materials to improve clinical efficiency.
The Senior Clinical Research Associate coordinates clinical monitoring and site management processes to ensure trial compliance with protocols and regulatory standards. They perform on-site and remote monitoring activities, manage documentation, and resolve site-related issues to ensure data reliability and subject safety.
You will coordinate all aspects of the clinical monitoring and site management process to ensure trial compliance with protocols and regulatory standards. This includes conducting remote or on-site visits, managing documentation, and ensuring data accuracy through rigorous review processes.
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Provide fast, accurate, and personalized medical advice to members via video teleconsultations and a medical chat service. Ensure high-quality patient care while maintaining a 4-hour response time for chat inquiries.
You will oversee and manage clinical trial activities to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice standards. Additionally, you will conduct site visits, provide training to staff, and collaborate with cross-functional teams to ensure accurate data collection.
You will coordinate clinical trial monitoring activities, including study setup, documentation maintenance, and site management. Additionally, you will ensure compliance with protocols and regulatory requirements to maintain patient safety and study cost efficiency.
The Senior Manager will lead global Medical Affairs strategies, fostering partnerships with Key Opinion Leaders and managing scientific evidence generation. They will also provide medical leadership throughout the product lifecycle and ensure all communications comply with regulatory and ethical standards.
The Clinical Research Associate II participates in the preparation and execution of Phase I-IV clinical trials while overseeing site evaluation, initiation, and monitoring activities. They ensure compliance with Good Clinical Practices and maintain data integrity through source verification and site correspondence.
The Principal Biostatistician serves as the statistical lead for late-phase clinical trials, providing scientific oversight and strategic guidance. They are responsible for authoring statistical analysis plans, performing complex analyses, and representing the biostatistics function within cross-functional clinical teams.
The specialist manages clinical trial site activities, including site activation, protocol training, and case coverage to ensure efficient study conduct. They also maintain strong relationships with investigators and provide continuous status updates to internal clinical trial leaders.
The Medical Director provides medical leadership for clinical trials, including protocol development, medical monitoring, and safety evaluation. They serve as the primary medical liaison between the sponsor and internal departments to ensure study compliance and effective issue resolution.
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 Lead Clinical Research Associate provides leadership to the CRA and CTA teams to ensure clinical trials are initiated and conducted according to SOPs and regulations. They act as the primary liaison between study sites and internal staff while managing clinical monitoring plans and project timelines.
The clinician will remotely administer semi-structured clinical interviews and cognitive assessment batteries to pediatric subjects and caregivers. They will also provide central monitoring by reviewing neuropsychological test data to ensure accuracy and provide feedback to other raters.
The Local Clinical Trial Manager is responsible for leading local study teams and ensuring clinical deliverables meet time, budget, and quality expectations. They serve as the operational point-of-contact, managing site selection, regulatory submissions, and vendor oversight to ensure study integrity.
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The role involves conducting patient interviews and clinical assessments while ensuring the integrity and reliability of clinical trial data. The rater will provide guidance to other raters on methodology and scoring techniques through live interactions.
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.
The Clinical Research Associate performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They are responsible for managing site activities, verifying clinical data accuracy, and maintaining essential study documentation.
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 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.
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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 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.
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