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The Senior Medical Science Liaison acts as a field-based scientific expert, building relationships with healthcare professionals and key opinion leaders to drive scientific exchange. They also support medical strategy, evidence generation, and cross-functional initiatives to ensure access to therapeutic innovations in rare neurological diseases.
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 Clinical Research Associate is responsible for site qualification, initiation, monitoring, and close-out visits to ensure protocol adherence and data integrity. They also provide mentorship to site staff and manage study documentation within the Trial Master File.
Provide compassionate tele-triage services by assessing patient symptoms and offering healthcare advice via phone. Document cases accurately using clinical software while adhering to safety protocols and maintaining professional patient interactions.
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.
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Manage investigative sites across Italy to ensure clinical trials adhere to study protocols, ICH-GCP, and regulatory requirements. Perform site monitoring visits, verify source data, and maintain Trial Master File documentation while supporting study staff.
The role involves conducting clinical monitoring visits to ensure data integrity and patient safety while maintaining compliance with regulatory standards. You will also manage Trial Master File documentation and coordinate site activities to support clinical study timelines.
The specialist is responsible for the end-to-end execution, negotiation, and maintenance of clinical site contracts and budgets. They will collaborate with cross-functional stakeholders to ensure compliance with fair market value principles and departmental standards.
The Manager of Clinical Operations oversees employee resources and project projections to ensure contractual obligations and client expectations are met. They also direct departmental performance metrics, mentor staff, and design cross-functional process efficiencies for clinical trials.
The Associate Manager is responsible for interviewing, selecting, and onboarding CRA/IHCRA candidates while ensuring they are properly trained and mentored. They also manage performance, review quality metrics, and act as a point of escalation for project-related issues.
The clinician will conduct remote semi-structured clinical interviews and cognitive assessments for pediatric subjects in clinical trials. They are also responsible for scoring assessments and providing central monitoring to ensure data accuracy and quality.
The Senior Clinical Research Associate II is responsible for site monitoring, site management, and ensuring adherence to study protocols and regulatory guidelines. They also act as a lead monitor, mentor junior staff, and coordinate clinical projects while maintaining data integrity.
The RN Care Manager will conduct home visits to assess health status and safety while providing clinical coaching and support to caregivers. They are responsible for developing individualized care plans, maintaining accurate documentation, and ensuring compliance with regulatory standards.
Conduct qualification, initiation, monitoring, and closeout visits at research sites to ensure protocol compliance and data accuracy. Manage communication with site staff and verify investigator qualifications, medical records, and investigational product accountability.
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 Construction Estimator will manage the full bidding process, including identifying opportunities, performing quantity takeoffs, and submitting competitive bids. They will also coordinate with stakeholders, handle RFIs and submittals, and participate in strategic planning meetings.
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The Medical Scientist Lead provides management supervision to staff and oversees medical monitoring activities for clinical projects. They collaborate with Medical Monitors to ensure compliance with regulatory standards and support the execution of study-related plans.
The Medical Director serves as the Global Lead Medical Monitor for clinical trials, providing therapeutic expertise and protocol-specific training to project teams. They also contribute medical input to clinical development programs and support business development activities through proposal generation and sponsor meetings.
The Associate Director manages, selects, and trains clinical management staff to ensure the successful execution of clinical deliverables within assigned projects. They are responsible for overseeing project strategies, managing budgets, and ensuring operational excellence across clinical programs.
The Clinical Research Associate will conduct site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance and patient safety. They will also collaborate with investigators and site staff while performing data review to maintain high-quality clinical data.
You will conduct clinical trial monitoring activities, including site visits and data review to ensure protocol compliance and patient safety. Additionally, you will collaborate with investigators and site staff while contributing to the preparation of essential study documentation.
You will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. Key tasks include monitoring clinical trial sites, conducting site visits, and collaborating with cross-functional teams to ensure accurate data collection.
The Senior Clinical Research Associate is responsible for the initiation, monitoring, and close-out of clinical study sites in accordance with SOPs and regulatory requirements. They will provide unmasked support, manage investigational product accountability, and ensure data integrity and protocol compliance throughout the study.
The Medical Director provides medical and scientific oversight for clinical research programs, serving as the primary medical monitor for sponsor companies. Responsibilities include protocol development, safety monitoring, SAE reporting, and providing medical input for clinical data and regulatory submissions.
The Senior Clinical Team Manager directs and coordinates the technical and operational aspects of clinical trials to ensure successful completion within budget and timelines. They manage clinical and start-up activities, lead project teams, and maintain compliance with ICH GCP and regulatory standards.
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The Clinical Specialist provides clinical support and product education to healthcare professionals to ensure optimal patient outcomes and drive sales. They collaborate with the sales team to identify customer needs and provide technical solutions for interventional procedures.
The Senior Clinical Research Associate is responsible for conducting site visits, ensuring compliance with FDA and ICH-GCP regulations, and managing regulatory documentation. Additionally, the role involves performing data verification, assisting with budget negotiations, and mentoring junior team members.
The Assistance Nurse manages medical cases for travelers by assessing calls and providing professional clinical advice. They coordinate care and transport while ensuring decisions align with duty of care standards and cost-effectiveness.
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.
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