Supports the delivery of an exceptional customer experience to private banking clients, providing professional service and managing client needs and transactions.
Compensation
$40,500.00 - $80,000.00
Responsibilities
Provides courteous, knowledgeable service to private banking clients
Identifies client needs and matches with appropriate products or services
Prepares new business proposals or presentations
Manages transaction processing and ensures timely completion
Takes ownership of client inquiries and resolves concerns
The Site Strategy Lead (SSL) is integral to the development of our delivery strategies at the very early phase of proposal development, and is a key player in supporting the study specific requests for the Data Generation group from the clients in the request for proposal.
Compensation
The potential base pay range for this role, when annualized, is $93,100.00 - $232,800.00. Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
Responsibilities
Assist with overall project efficiency and adherence to project timelines and financial goals
Assist with turning a study budget and strategy into action that make RWE studies more predictable, shorten timelines, improve data quality and provide innovative solutions to the clients
Act as a single functional lead for Data Generation proposals, covering Site ID, Site and Patient Engagement, Site Management and Technology strategies
Partners with internal teams to understand relevant challenges within a study and to identify the Data Generation strategies that can help meet these challenges
Serves as single point of contact on the study to answer pre and post award site strategy questions
Senior Clinical Research Associate responsible for ensuring clinical trial quality, data integrity, patient safety, and regulatory compliance at site level, primarily in oncology trials, through remote and on-site monitoring.
Locations (2)
Marseille, Provence-Alpes-Côte d'Azur, France
Aix-en-Provence, Provence-Alpes-Côte d'Azur, France
Responsibilities
Ensure compliance with study protocols, ICH-GCP guidelines, regulatory requirements, and company procedures across assigned sites.
Evaluate site performance and provide recommendations for site-specific actions, escalating significant issues and supporting development of corrective action plans when required.
Verify that informed consent processes are appropriately conducted and documented for each study participant.
Assess patient safety and clinical data integrity by identifying protocol deviations, violations, pharmacovigilance concerns, and other site-level risks.
Conduct monitoring activities through remote and on-site methods in accordance with the Clinical Monitoring Plan and Study Monitoring Plan.
Senior Clinical Research Associate responsible for ensuring compliance, data integrity, and regulatory adherence in oncology clinical trials, conducting remote and on-site monitoring.
Locations (3)
Marseille, Provence-Alpes-Côte d'Azur, France
Aix-en-Provence, Provence-Alpes-Côte d'Azur, France
France
Responsibilities
Ensure compliance with study protocols, ICH-GCP guidelines, regulatory requirements, and company procedures across assigned sites.
Evaluate site performance and provide recommendations for site-specific actions, escalating significant issues and supporting development of corrective action plans when required.
Verify that informed consent processes are appropriately conducted and documented for each study participant.
Assess patient safety and clinical data integrity by identifying protocol deviations, violations, pharmacovigilance concerns, and other site-level risks.
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