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.
Remote Clinical Research Jobs (1,610)
Tags = clinical-research
The role involves developing and maintaining clinical data collection standards libraries in compliance with CDISC and regulatory requirements. The consultant will act as a subject matter expert for studies in China and provide guidance on standards implementation across clinical data management activities.
Senior Clinical Project Manager or Project Manager II - Oncology
Fortrea
·
Full Time
·
1 Week Ago
Fortrea
The Senior Project Manager oversees domestic and global oncology projects, managing teams, budgets, risks, and stakeholder communications to ensure operational excellence. They are also responsible for regulatory documentation, line management of staff, and supporting business development efforts.
The SSU Associate coordinates clinical trial site start-up activities, focusing on the preparation, submission, and approval of regulatory documents and Informed Consent Forms. They manage site readiness, track metrics in CTMS and eTMF, and ensure compliance with global regulatory standards.
The SSU Associate coordinates clinical trial site start-up activities, focusing on the preparation and approval of regulatory documents and IRB submissions. They manage essential document collection and customize Informed Consent Forms while maintaining site metrics in CTMS and eTMF systems.
New remote clinical research jobs delivered to your inbox
We'll notify you when new positions matching this search are posted
Provides leadership for the conduct of clinical studies and regulatory affairs to ensure timely product approvals and scientific validity. Manages a team of employees, focusing on performance management, talent development, and the execution of local and global clinical research projects.
Lead the clinical operations strategy and execution of global clinical trials, ensuring they are delivered on time, within budget, and according to quality standards. Serve as the primary clinical liaison for sponsors and coordinate cross-functional teams across various regions and time zones.
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 for accurate data collection.
Registered Pharmacy Technician RX To Go
Florida Cancer Specialists
·
Full Time
·
1 Week Ago
Florida Cancer Specialists
The role involves performing pharmacy technician functions across intake, adherence, revenue, and dispensing teams, specifically focusing on oral oncology medications. Key duties include insurance verification, therapy adherence documentation, billing resolution, and accurate medication dispensing under pharmacist supervision.
Associate Manager / Manager, Project Services - Laboratories (Remote - West Coast)
IQVIA
·
Full Time
·
1 Week Ago
IQVIA
Manage all laboratory aspects of clinical trial projects from award through closeout, serving as the primary point of contact for sponsors. Lead project planning, risk management, and cross-functional coordination to ensure high-quality execution and protocol compliance.
Associate Manager / Manager, Project Services - Laboratories (Remote - East Coast)
IQVIA
·
Full Time
·
1 Week Ago
IQVIA
Manage all laboratory aspects of clinical trial projects from award through closeout, serving as the primary point of contact for sponsors. Lead project planning, risk management, and cross-functional coordination to ensure high-quality execution and protocol compliance.
Research Navigator, Consults and Grants (Neurology)
Johns Hopkins University
·
Full Time
·
1 Week Ago
Johns Hopkins University
The Research Navigator manages the protocol optimization process and end-to-end grant production for clinical research in Neurology. They serve as a liaison between investigators and leadership to ensure high-quality study design and successful funding outcomes.
The Senior Clinical Scientist will lead the execution of Phase 2 and 3 clinical trials in nephrology, focusing on protocol development and scientific oversight. They will manage data review, medical monitoring, and collaborate cross-functionally to ensure regulatory compliance and data quality.
The Medical Director provides strategic medical leadership and expert scientific consultation throughout project lifecycles. They are responsible for ensuring compliance with regulatory standards and representing the Medical Affairs Department in business development initiatives.
The Clinical Trial Manager is responsible for planning and managing all aspects of clinical trials, ensuring adherence to timelines, budgets, and quality standards. They collaborate with cross-functional teams and investigators to implement protocols and ensure compliance with international regulations.
Define and implement a regulatory-grade Real World Data (RWD) strategy and pipeline to support clinical development and digital health products. Lead a multi-disciplinary informatics team to transform complex datasets like EHR and claims into research-ready assets using AI and automation.
The Director will drive cross-functional process improvements across clinical research operations to accelerate study activation and increase patient accrual. They will act as the primary bridge between research operations and the technology team to translate process designs into automated solutions and AI tools.
New remote clinical research jobs delivered to your inbox
We'll notify you when new positions matching this search are posted
Design and lead real-world evidence studies to connect health signals to outcomes, healthcare utilization, and cost savings. Collaborate with data science and external partners to produce rigorous research outputs for clinical and commercial audiences.
The Coder Physician is responsible for abstracting, coding, and sequencing clinical information from various medical records to ensure accurate reimbursement and reporting. They must maintain a 95% quality rating while complying with HIPAA and regulatory standards in a remote environment.
Oncology Data Specialist
Omega Healthcare Solutions
·
Full Time
·
1 Week Ago
Omega Healthcare Solutions
The Oncology Data Specialist is responsible for abstracting detailed cancer case information from electronic medical records into registry software. They ensure compliance with state and national reporting standards while performing case finding and follow-up duties.
Identify and recruit eligible participants for clinical research studies through various channels and medical records. Educate potential participants on trial procedures and obtain informed consent while maintaining detailed regulatory records.
Oversee and manage clinical trial activities to ensure adherence to protocols, regulatory requirements, and GCP standards. Lead monitoring tasks, conduct site visits, and collaborate with cross-functional teams for accurate data collection.
The Senior CRA will oversee clinical trial activities to ensure adherence to protocols, regulatory requirements, and GCP standards. Key tasks include conducting site visits, managing data collection, and providing guidance to site staff and other CRAs.
Oversee and manage clinical trial activities to ensure adherence to protocols, regulatory requirements, and GCP standards. Lead monitoring tasks, conduct site visits, and collaborate with cross-functional teams for accurate data reporting.
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.
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.
New remote clinical research jobs delivered to your inbox
We'll notify you when new positions matching this search are posted
Oversee and manage clinical trial activities to ensure adherence to protocols, regulatory requirements, and GCP standards. Lead monitoring tasks, conduct site visits, and collaborate with cross-functional teams for accurate data collection.
Oversee and manage clinical trial activities to ensure adherence to protocols, regulatory requirements, and GCP standards. Lead monitoring tasks, conduct site visits, and collaborate with cross-functional teams to ensure accurate data collection.
The Senior CRA oversees clinical trial activities to ensure adherence to protocols, regulatory requirements, and GCP standards. Key tasks include monitoring sites, conducting visits, and collaborating with cross-functional teams for accurate data reporting.
The Senior CRA oversees clinical trial activities to ensure adherence to protocols, regulatory requirements, and GCP standards. Key tasks include conducting site visits, managing data collection, and providing guidance to site staff and other CRAs.
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
