The Principal Statistical Programmer develops and validates complex datasets and outputs using SAS programming, ensuring compliance with CDISC standards like ADaM and SDTM models. This role also involves collaborating with cross-functional teams, providing technical guidance, and mentoring junior programmers.
Remote Clinical Research Jobs (612)
Tags = clinical-research
As a Clinical Research Associate, you will act as the main line of communication between the project team, sponsor, and site while ensuring quality standards in clinical studies. You will prepare and conduct monitoring visits, manage subject recruitment, and ensure compliance with study protocols.
Clinical Enrollment Manager - UK - 0.3FTE
Innovative Trials
·
Full Time
·
23 Weeks Ago
Innovative Trials
The Clinical Enrollment Manager will boost patient recruitment for clinical trials through tailored site optimization services and provide hands-on support to alleviate recruitment burdens. Responsibilities include community outreach, site optimization calls, and maintaining engagement with trial sites.
Clinical Research Budget Manager, Office of Research and Project Administration
Memorial Sloan Kettering Cancer Center
·
Full Time
·
24 Weeks Ago
Memorial Sloan Kettering Cancer Center
The Clinical Research Budget Manager will develop and lead budgets for clinical research studies, ensuring compliance with regulations and alignment with funding sources. They will also negotiate budgets with industry sponsors and provide guidance on budgetary matters to faculty.
Clinical Trial Manager (Cardiovascular/Endocrine/Metabolic) - Lyon
Medpace, Inc.
·
Full Time
·
24 Weeks Ago
Medpace, Inc.
Manage day-to-day operations of clinical trial projects and serve as the primary contact for operational issues. Ensure compliance with ICH/GCP regulations and maintain knowledge of the therapeutic area and protocol.
New remote clinical research jobs delivered to your inbox
We'll notify you when new positions matching this search are posted
Clinical Compliance Manager
Thermo Fisher Scientific
·
Full Time
·
24 Weeks Ago
Thermo Fisher Scientific
The Clinical Compliance Manager leads the assessment and classification of serious breaches in clinical trials and serves as the primary contact for breach investigations. This role also involves preparing notifications for regulatory authorities and developing standard operating procedures related to breach management.
Clinical Research Associate (Contract) 11 APPLICANTS
Priovant Therapeutics
·
Full Time
·
24 Weeks Ago
Priovant Therapeutics
The Clinical Research Associate will conduct site visits and manage site activities to ensure compliance with regulatory guidelines and project timelines. They will also interact with clinical site staff to resolve issues and ensure the validity of study data.
Typical responsibilities involve performing site selection, initiation, monitoring, and close-out visits, along with maintaining necessary documentation and supporting the development of a subject recruitment plan. The role also includes establishing communication lines, administering protocol training, evaluating site quality, and managing progress tracking for submissions, recruitment, and data resolution.
The Associate Director manages the Interventional Biostatistics team operations, overseeing personnel, quality assurance, resource planning, and financial performance to ensure effective statistical services for interventional clinical trials. This role also involves representing the group in business development efforts, advancing the product line, and mentoring team members.
The role involves conducting targeted sales calls to dental professionals and managing territory activities to drive sales performance. Additionally, the representative will engage in professional education and support initiatives to build strong partnerships within the dental community.
The Sales Lead will lead field-based activities across Gauteng, conducting high-quality sales calls and delivering professional detailing. They will also engage with dental professionals and manage territory budgets while providing exceptional customer service.
The Global Clinical Project Specialist will be a key member of the sponsor's Global Study Team, responsible for delivering clinical studies on time, within budget, and ensuring quality. This includes oversight of study eTMF completeness, budget management, vendor management, and data oversight.
Clinical Research Associate/Senior Clinical Research Associate- FSP
Parexel
·
Full Time
·
25 Weeks Ago
Parexel
The Clinical Research Associate (CRA) is responsible for the delivery of studies at allocated sites, including preparation, initiation, monitoring, and closure of assigned sites. The CRA acts as the main contact with the study site and ensures compliance with international guidelines and local regulations.
Clinical Trial Manager (Associate Director) - Stirling
Medpace, Inc.
·
Full Time
·
25 Weeks Ago
Medpace, Inc.
The Clinical Trial Manager will manage day-to-day operations of clinical projects and serve as the primary contact for operational issues. They will also provide oversight of project team members and ensure compliance with applicable regulations.
The Clinical Research Associate will conduct site qualification, initiation, monitoring, and close-out visits for clinical trials while ensuring protocol compliance and patient safety. They will also collaborate with investigators and site staff to facilitate smooth study conduct and perform data review.
French Speaking Medical Information Specialist - Graduate Opportunity
ProPharma
·
Full Time
·
25 Weeks Ago
ProPharma
The role involves responding to medical and safety-related inquiries from healthcare professionals and patients, documenting adverse events, and providing accurate information based on approved resources. Additionally, the specialist will support service quality and contribute to process improvements.
The Site Management Associate will coordinate monitoring activities at clinical trial sites and assist in ensuring compliance with study protocols and regulatory requirements. They will also track site performance metrics and provide reports to enhance site management efficiency.
New remote clinical research jobs delivered to your inbox
We'll notify you when new positions matching this search are posted
The Senior Clinical Research Associate (Sr CRA) conducts site monitoring for clinical trials, ensuring compliance and quality while providing oversight and guidance to the CRA team. Responsibilities include managing study budgets, preparing monitoring reports, and maintaining communication with study sites.
Conduct on-site and remote monitoring of clinical research studies to ensure compliance with clinical practices and study protocols. Collaborate with cross-functional teams to support clinical trial activities and manage the work of lower-level professionals.
Principal Medical Scientist (Project Lead) - RWE - Poland, Bulgaria, Romania, Spain, UK - Sponsor-dedicated
Syneos Health
·
Full Time
·
25 Weeks Ago
Syneos Health
The Principal Medical Scientist manages project scope, objectives, and quality of deliverables while serving as the primary interface between internal teams, customers, and vendors. They also provide scientific oversight and contribute to the planning and development of medical monitoring and scientific services activities.
The Site Lead will oversee a designated site, collaborating with senior leadership to drive clinical and quality performance. Duties include daytime coverage of outpatient and hospital inpatient examinations.
Clinical Subject Matter Expert
Pharmavise Corporation
·
Full Time
·
26 Weeks Ago
Pharmavise Corporation
Serve as the primary clinical expert within the organization, providing guidance across clinical development programs. Monitor ongoing clinical trials for protocol adherence and patient safety while collaborating with cross-functional teams.
Clinical Trial Manager - Germany - Neuroscience / Ophthalmology
Medpace, Inc.
·
Full Time
·
26 Weeks Ago
Medpace, Inc.
Manage day-to-day operations of clinical trial projects and serve as the primary contact for sponsors regarding operational issues. Ensure compliance with ICH/GCP regulations and maintain knowledge of protocols and therapeutic areas.
Clinical Trial Manager - UK (London, Stirling) - Neuroscience / Ophthalmology
Medpace, Inc.
·
Full Time
·
26 Weeks Ago
Medpace, Inc.
Manage day-to-day operations of clinical trial projects and serve as the primary contact for sponsors. Ensure compliance with ICH/GCP regulations and maintain knowledge of protocols and therapeutic areas.
Clinical Trial Manager - France - Neuroscience / Ophthalmology
Medpace, Inc.
·
Full Time
·
26 Weeks Ago
Medpace, Inc.
Manage day-to-day operations of clinical trial projects and serve as the primary contact for operational issues. Oversee internal project team members and ensure compliance with protocols and regulations.
Manage day-to-day operations of clinical trial projects and serve as the primary contact for operational issues. Ensure compliance with ICH/GCP regulations and maintain oversight of project team deliverables.
New remote clinical research jobs delivered to your inbox
We'll notify you when new positions matching this search are posted
Manage day-to-day operations of clinical trial projects and serve as the primary contact for operational issues. Ensure compliance with ICH/GCP regulations and maintain oversight of project deliverables.
Manage day-to-day operations of clinical trial projects and serve as the primary contact for operational issues. Ensure compliance with ICH/GCP regulations and maintain knowledge of the therapeutic area.
Clinical Trial Manager (Cardiovascular/Endocrine/Metabolic) - London
Medpace, Inc.
·
Full Time
·
26 Weeks Ago
Medpace, Inc.
The Clinical Trial Manager will manage day-to-day operations of clinical projects, ensuring compliance with ICH/GCP regulations. They will serve as the primary contact for sponsors and oversee internal project team deliverables.
Clinical Trial Manager (Oncology/Cardiovascular/Endocrine/Metabolic)
Medpace, Inc.
·
Full Time
·
26 Weeks Ago
Medpace, Inc.
Manage day-to-day operations of clinical trial projects and serve as the primary contact for operational issues. Ensure compliance with ICH/GCP regulations and maintain knowledge of the protocol and therapeutic area.
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
