2,268 Clinical Research jobs available for remote work from home. Apply for positions such as Field Clinical Advisor - Cell Therapy - Chicago (IL/WI/IN/MN), Clinical Research Associate - French Speaking - Any EMEA location, Senior Regulatory Affairs Associate, and more! Discover the best work-from-home or hybrid, full- and part-time jobs.
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The Field Clinical Advisor drives the execution of cell therapy clinical trials by managing site recruitment, retention, and safety protocols. They also serve as a primary field point for protocol issues and provide educational support to optimize patient outcomes and data quality.
The Clinical Research Associate manages clinical site monitoring responsibilities, ensuring adherence to Good Clinical Practice and regulatory guidelines. They serve as the primary point of contact for sites, tracking study metrics and performing quality reviews of study documentation.
The Senior Regulatory Affairs Associate is responsible for preparing, reviewing, and submitting regulatory documents such as CTAs and INDs to agencies like Health Canada and the FDA. They also manage regulatory intelligence, maintain submission databases, and ensure compliance with evolving regulatory guidelines.
The Senior Contracts Manager will review, analyze, and negotiate clinical trial contracts and vendor agreements to ensure regulatory compliance. They will also collaborate with cross-functional teams to assess risks and provide guidance on contract interpretation and dispute resolution.
The Senior Clinical Research Associate coordinates clinical monitoring and site management processes to ensure trial compliance with protocols and regulatory standards. They perform risk-based monitoring, manage site documentation, and facilitate communication between investigative sites and the project team.
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The Clinical Research Associate will coordinate clinical monitoring and site management processes to ensure trial compliance with protocols and regulatory standards. They will perform risk-based monitoring, manage site documentation, and facilitate communication between investigative sites and the project team.
You will own the vision, strategy, and multi-year roadmap for clinical AI products, ensuring they integrate seamlessly into clinician workflows. You will partner with data science, clinical affairs, and regulatory teams to guide algorithms from research through FDA-regulated development to launch.
The Academic Partnerships Director will build and manage relationships with principal investigators and research institutions to drive adoption of the Beacon Platform in grant-funded studies. This role involves identifying partnership opportunities, supporting proposal development, and managing the full sales cycle for academic and research accounts.
The Regional Clinical Study Manager is accountable for regional study delivery, ensuring quality, inspection readiness, and adherence to timelines and budgets. They lead the regional clinical operations team, manage external vendors, and act as the primary point of escalation for study-related issues.
The Regional Clinical Study Manager is accountable for regional study delivery, ensuring quality, inspection readiness, and adherence to timelines and budgets. They lead the regional clinical operations team, manage external vendors, and act as the primary point of escalation for study-related issues.
The Clinical Research Manager acts as a line manager for trial monitoring staff, overseeing their performance, training, and professional development. They are responsible for managing study start-up activities, ensuring adherence to ICH/GCP guidelines, and collaborating with regional operations to meet study timelines and quality standards.
The role involves line managing clinical study managers, overseeing their performance, and ensuring clinical trials are executed according to ICH/GCP guidelines and corporate standards. The manager will also drive process improvements, allocate resources, and provide local expertise to support clinical trial activities.
The Insurance Follow-up Specialist manages billing and collections for hospitals and physicians by acting as an intermediary between institutions, patients, and insurance agencies. Responsibilities include filing claims, managing denials, determining reimbursements, and resolving complex patient account issues.
The Training Specialist facilitates professional training events for customers and internal employees on Advarra software. They are also responsible for creating and maintaining training materials, documentation, and eLearning modules.
The Medical Director provides medical leadership and strategic direction for clinical development programs, ensuring study protocols meet scientific and regulatory standards. They serve as a Medical Monitor, interpret clinical trial data, and collaborate with multidisciplinary teams to drive successful program execution.
The Principal Statistician oversees biostatistics personnel, develops training plans, and ensures the timely delivery of high-quality statistical outputs for clinical trials. They act as a lead biostatistician, collaborating with sponsors and regulatory agencies while ensuring compliance with SOPs and ICH guidelines.
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The Medical Science Liaison will serve as a scientific expert, building partnerships with oncology healthcare professionals and facilitating evidence-based discussions. They are responsible for capturing medical insights, supporting research activities, and contributing to medical affairs planning.
The Contract Analyst II is responsible for reviewing, analyzing, and negotiating clinical trial contracts and vendor agreements to ensure regulatory compliance. They also collaborate with cross-functional teams to manage contract risks and maintain accurate records within contract management systems.
You will monitor and own the progress of clinical studies at investigative sites to ensure compliance with protocols, SOPs, and ICH-GCP standards. Additionally, you will coordinate study setup activities, including investigator identification and regulatory submissions.
You will monitor and own the progress of clinical studies at investigative sites to ensure compliance with protocols, SOPs, and ICH-GCP standards. Additionally, you will coordinate study setup activities, including investigator identification and regulatory submissions.
The Lead Clinical Trials Program Manager will oversee the planning, coordination, and execution of decentralized clinical trials for federal health agencies. This role involves managing regulatory compliance, facilitating stakeholder engagement, and ensuring data integrity throughout the study lifecycle.
The Clinical Sales Specialist provides clinical and technical support to interventional cardiologists and catheter lab staff during procedures. They also educate customers on product usage and collaborate with territory managers to drive sales strategies.
The Clinical Sales Specialist provides clinical and technical support to physicians and catheter lab staff during structural heart procedures. They also collaborate with territory managers to educate customers on product usage and implement marketing strategies.
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The Technical Program Manager will lead the implementation and delivery of mpathic's solutions across clinical research programs and healthcare studies. They will serve as the primary operational point of contact, managing project timelines, site training, and cross-functional coordination between engineering, product, and clinical teams.
The Solution Implementation Lead serves as the end-to-end execution owner for developing and operationalizing connected medical device and digital health solutions. They coordinate cross-functional teams including engineering, IT, and regulatory to ensure solutions are ready for scalable study deployment.
The Clinical Sales Specialist provides clinical and technical support to physicians and catheter lab staff during structural heart procedures. They also collaborate with territory managers to educate customers on product usage and contribute to the implementation of marketing strategies.
This role serves as the primary application owner for Epic Research, managing strategic advances, system upgrades, and API integrations. The individual will collaborate with clinical research leadership and support groups to align workflows and ensure the health and effective usage of the application.
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