Manage the full lifecycle of sponsored projects, including the development and submission of grant proposals and the detailed reconciliation of project budgets. Ensure all activities comply with federal regulations and university policies while guiding faculty and principal investigators.
Remote Clinical Research Jobs (607)
Tags = clinical-research
Lead a complex grants and contracts portfolio by coordinating pre-award proposal submissions and post-award financial reconciliation. Manage compliance, budget projections, and partnerships across multiple disciplines and faculty within the School of Medicine.
Manage Site Enrollment and Engagement Lead (SEEL) teams to optimize clinical trial enrollment and ensure compliance with regulations. Deliver regular project updates, conduct performance reviews, and support the recruitment and training of SEEL staff.
Drive the planning and execution of clinical study start-up activities to ensure trials are launched efficiently and compliantly. Lead cross-functional teams and manage internal and external resources to meet timelines, budget, and quality standards.
Director, Medical Science Liaison, Oncology (Dallas, AR, LA, OK, MS)
Revolution Medicines
·
Full Time
·
4 Days Ago
Revolution Medicines
The Director, MSL will engage in peer-to-peer scientific dialogue with healthcare professionals and KOLs to gather insights and advance medical knowledge. They will serve as a therapeutic expert and liaison between the company and clinical study sites to support medical strategies and congresses.
New remote clinical research jobs delivered to your inbox
We'll notify you when new positions matching this search are posted
The role serves as the primary sponsor point of contact for investigative sites, ensuring trial conduct complies with protocols and regulatory standards. Responsibilities include conducting site monitoring, mentoring junior CRAs, and managing risk assessments to ensure patient safety and data integrity.
Vice President, Site Activation Project Management and Global Regulatory Oversight
ICON plc
·
Full Time
·
4 Days Ago
ICON plc
Provide strategic and operational leadership for the global study start-up organization to ensure timely and compliant initiation of clinical trials. Lead global teams in site activation and regulatory oversight while serving as the executive sponsor for delivery excellence across pharma and biotech portfolios.
Regulatory Assistant - Clinical Trials Office
The Ohio State University
·
Full Time
·
4 Days Ago
The Ohio State University
Provides regulatory support to ensure research protocols comply with university, state, and federal regulations. Responsibilities include preparing IRB submissions, maintaining regulatory files, and managing data within the OnCore database.
The Data Management Lead provides technical expertise and serves as the primary point of contact for assigned studies to ensure quality and timely delivery of data. Responsibilities include managing study timelines, collaborating with cross-functional global teams, and ensuring compliance with regulatory guidelines.
Responsible for identifying and screening potential clinical trial participants via outbound and inbound calls. Tasks include assessing eligibility based on protocol criteria and scheduling qualified candidates for on-site visits.
The Billing Manager oversees all accounts receivable functions, including invoicing, collections, and account reconciliations for sponsors. They lead the billing team and partner with Project Managers and Finance to optimize billing operations and ensure compliance with contract terms.
Drive revenue growth by securing new clients and expanding services for global clinical operations. Manage the full sales lifecycle from prospecting and relationship building to closing complex, high-value deals.
Manage start-up contracting activities, including developing investigator grant estimates and maintaining contract templates for biotech sponsors. Ensure compliance with regulatory requirements and project timelines while collaborating with stakeholders and RSU regions.
Conducts reviews of human subject research applications to ensure compliance with federal regulations, HRO policies, and ethical standards. Provides regulatory consultation to investigators and assists in the development of educational initiatives and institutional policies.
The Principal Statistical Programmer leads clinical sub-teams by delegating tasks, providing technical support, and ensuring the accuracy of SAS code and output. They are responsible for creating necessary files and analyses for electronic submissions in eCTD format while ensuring compliance with FDA/ICH/GCP regulations.
Registered Pharmacy Technician RX To Go
Florida Cancer Specialists
·
Full Time
·
4 Days Ago
Florida Cancer Specialists
Perform routine pharmacy technician functions including insurance verification, therapy adherence documentation, and prescription billing. Responsible for the accurate dispensing, packaging, and shipping of oral oncology medications under pharmacist supervision.
Design and implement advanced clinical systems and programming solutions for CDMS, including data validation and custom reports. Collaborate with cross-functional teams to integrate these solutions into the overall data management process and mentor junior programmers.
New remote clinical research jobs delivered to your inbox
We'll notify you when new positions matching this search are posted
The Local Trial Manager is responsible for end-to-end trial delivery at the country level, serving as the primary point of contact for internal partners. Key duties include managing local vendors, overseeing milestones from feasibility to close-out, and ensuring inspection readiness.
Acts as the primary point of communication for clinical sites to streamline operations and ensure trial compliance throughout the lifecycle. Manages site selection, recruitment targets, budget forecasting, and ensures high standards of data quality and inspection readiness.
Serve as the primary point of contact for 20-30 small pharmaceutical accounts to drive client satisfaction and revenue growth. Manage day-to-day interactions, commercial administration, and the adoption of IQVIA's data assets and commercial offerings.
Senior Clinical Research Associate (Level I)
Thermo Fisher Scientific
·
Full Time
·
4 Days Ago
Thermo Fisher Scientific
The Senior CRA coordinates clinical monitoring and site management to ensure trial compliance with protocols, ICH-GCP guidelines, and regulatory requirements. Responsibilities include conducting remote or on-site visits, managing documentation, and maintaining collaborative relationships with investigational sites.
Clinical Research Financial Analyst II
Children's Hospital of Philadelphia
·
Full Time
·
4 Days Ago
Children's Hospital of Philadelphia
Develop, coordinate, and negotiate financial budgets for NIH and pharmaceutical sponsored clinical research trials. Resolve issues related to billing, milestones, and payments while serving as a budgeting resource for clinical projects.
Acts as the primary end-to-end partner for clinical sites to streamline communication and ensure trial compliance. Manages site recruitment, budget forecasting, vendor oversight, and ensures high-quality data collection and inspection readiness.
The Sourcing Analyst drives strategic sourcing and procurement initiatives to identify cost-saving opportunities and strengthen supplier relationships. They manage procurement projects from planning through implementation and support the Cornell Experience Modernization Initiative (CEMI).
Responsible for all aspects of study site monitoring, including routine monitoring, close-out visits, and site management. Ensures the protection of study participants and the integrity of clinical trial data through rigorous verification and reporting.
AD Project Management - Neurosciences PL People Manager Role - Remote based in the US
Thermo Fisher Scientific
·
Full Time
·
4 Days Ago
Thermo Fisher Scientific
Directs a team of Project Delivery professionals, overseeing their career development, performance management, and technical coaching. Collaborates with stakeholders to align training needs and ensure successful completion of clinical trials within the Neurosciences therapeutic unit.
New remote clinical research jobs delivered to your inbox
We'll notify you when new positions matching this search are posted
Medical Director/Sr Medical Director - Pulmonary
Thermo Fisher Scientific
·
Full Time
·
4 Days Ago
Thermo Fisher Scientific
Provide medical oversight for clinical trials to ensure compliance with SOPs, GCP, and regulatory requirements. Perform medical review of safety data, adverse events, and clinical trial deliverables such as CSRs and periodic safety reports.
Responsible for creating and coordinating key clinical documents including protocols, clinical study reports, and investigator brochures. The role involves collaborating with clinical teams and managing medical writing deliverables to ensure regulatory compliance.
The Senior Account Executive is responsible for fostering client relationships and managing the end-to-end sales process to drive revenue growth. They collaborate with cross-functional teams to deliver high-quality services and monitor account performance to ensure client satisfaction.
Lead the strategy and execution of Oncology site network development and relationship management for clinical trials. Collaborate with cross-functional teams to enhance bid scenarios and monitor post-award delivery to ensure timely trial start-up.
Automatically Apply to the Best Remote Jobs
Stop the endless job search. Our AI finds and applies to the best jobs for you.
Browse Jobs by Role
Remote Data Analyst Jobs
Remote Management Consultant Jobs
Remote Account Executive Jobs
Remote Call Center Representative Jobs
Remote Graphic Designer Jobs
Remote Social Media Manager Jobs
Remote Proofreader Jobs
Remote Program Manager Jobs
Remote Video Editor Jobs
Remote Translator Jobs
Remote Technical Writer Jobs
Remote Customer Success Manager Jobs
Remote Software Engineer Jobs
Remote Content Creator Jobs
Remote Chief of Staff Jobs
