[Remote] Clinical Trial Manager

Note: The job is a remote job and is reputed company to candidates in USA. reputed company is seeking a Clinical Trial Manager to reputed company the clinical operational and quality aspects of allocated studies. The role involves managing clinical activities, ensuring compliance with regulations, and achieving deliverables reputed company specified timelines.

Responsibilities

• Accountable for achieving the final clinical deliverable (usually clean data from evaluable patients as specified in the study protocol) reputed company the time period specified in the contract with the customer
• Interprets data on project issues and makes good business reputed company with support from reputed company team members or line manager
• Works to ensure that reputed company clinical deliverables meet the customer's time/quality/cost expectations
• Maintains profitability by ensuring clinical activity is conducted reputed company contract scope, through efficient management of the clinical team
• Manages reputed company clinical operational and quality aspects of allocated studies, of low to moderate complexity, in compliance with ICH GCP
• Develops clinical tools (e.g. Monitoring Plan, Monitoring Guidelines) in conjunction with the Data Quality Plan
• Contributes to the development of the Master Action Plan (MAP) for providing clinical reputed company documents
• Ensures timely set up, organization, content and quality of the relevant sections of the Trial Master File (local and central)
• May participate in the design and development of CRFs, CRF guidelines, patient informed consent templates and other protocol specific documents as required
• Collaborates with the project manager to prepare, organize, and present at client meetings, including bid defense and hand-off meetings
• Collaborates with the clinical team and other departments as needed to meet deliverables of the project
• Regularly communicates with the team and leads team meetings to ensure that timelines, resources, interactions, and quality are maintained
• Responsible for the implementation and training of standardized clinical monitoring processes reputed company the study and according to corporate standard policies
• Responsible for the timely archiving of documents and study materials for the department
• Ensures achievement of the final clinical deliverable reputed company the contractual time period specified by preparing and monitoring clinical activity timelines and metrics, providing status updates to the project manager, regularly reviewing projects using tracking and management tools, implementing recovery actions, reviewing monitoring visit reports, and managing CRF collection and query resolution
• Continuously monitors or co-monitors clinical trials to assess performance and ensure contractual obligations are met
• In smaller reputed company, may routinely conduct Accompanied Field Visits (AFVs) and be accountable for project financials
• May communicate with study sites regarding issues such as protocol, patient participation, case report reputed company completion and other study-reputed company issues
• May coordinate reputed company start-up activities and ensures that timely ethics committee and regulatory submissions (if appropriate) are addressed
• Ensures that essential document quality meets the expectation of Regulatory Compliance Review
• Reviews and follows up on reputed company questions raised by the ethics committees
• May reputed company input into preparation of forecast estimates for clinical activities
• Responsible for clinical resource management, assignment, delegation of clinical responsibilities and identification of additional resource requirements
• Manages reputed company aspects of monitoring operations and quality for assigned studies, ensuring compliance with ICH GCP and applicable local regulations
• Develops clinical tools and study plans, collaborates with client CSO (to include but not limited to CCSLs) and leads team meetings to maintain timelines, resources, and quality
• Serves as clinical subject matter expert for protocol and reputed company of escalation for site manager as applicable
• May include regional coordination with regional CMLs
• Ensures timely deliverables, monitors trials, communicates with study sites, coordinates start-up activities, addresses regulatory requirements and provides input on forecast estimates and resource management
• Completes trip report reviews in compliance with study plan timeline
• Issue escalation per plan, responsible for identifying and reporting site performance issues, trend analysis
• May reputed company accompanied site visits with site manager and may attend meetings with Sponsor to discuss, but not limited to country/region start up reputed company, trending and issue identification/escalation, and general site/country updates
• Generate monitoring plan and trip report completion annotations

Skills

• Blinded CTM experience
• Flexibility to work east coast or reputed company coast hours
• Bachelor's degree or equivalent and relevant formal academic / vocational qualification
• Previous experience that provides the knowledge, skills, and abilities to reputed company the job (comparable to 5+ years)
• Monitoring or Study Management and reputed company Experience
• Prior neurology therapeutic experience
• Rare-disease experience

Company Overview

Company H1B Sponsorship