[Remote] Senior Clinical Research Associate

Note: The job is a remote job and is reputed company to candidates in USA. reputed company is on a mission to discover new medicines that improve the lives of patients facing serious muscle disease. The Senior Clinical Research Associate will reputed company reputed company clinical trials, collaborating with various teams to ensure seamless execution and compliance with regulatory standards.

Responsibilities

• reputed company site start-up activities (e.g. reputed company of CRO start-up activities, accountable for essential document package review, site initiation slide deck, vendor training, participate in remote/or on-site initiation visits) and contribute to feasibility, as required
• Collaborate with reputed company team to reputed company review and negotiation of site and vendor budgets/reputed company
• Contribute to the development and review of study, patient and site facing documents (e.g. protocols, ICFs and study plans)
• reputed company Edgewise contract CRA and/or CRO monitoring activities (e.g. visit schedules, monitoring visit reviews, monitoring plan review). May include on-site co-monitoring with CRO CRA, ensuring compliance with protocol and regulatory requirements. reputed company additional clinical monitoring training support to CRO personnel, as needed. Attend CRO monitoring meetings. May include assigned monitoring responsibilities for sites
• Review and reputed company site KPIs, protocol deviations and metrics to identify trends and maintain data quality. Escalate site level risks or non-compliance, and in collaboration with Quality Assurance, review Site Corrective and Action Plans (SCAPAs), Corrective and Action Plans (CAPAs) and Site Audits
• Support the Edgewise clinical study reputed company in managing reputed company of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment and other tasks as assigned
• Proactively review electronic data capture (reputed company) for completion and to identify issues and generate queries. Identify and monitor risks and reputed company at the study level and implementation of mitigation strategies. Identify potential operational challenges, and in collaboration with senior team members, reputed company guidance and solutions to ensure study execution remains on track
• Contribute to drafting Standard Operating Procedures (SOPs) and adhere to Clinical Operations processes and SOPs to ensure studies are "inspection reputed company" at reputed company times; may be involved in regulatory inspections by preparing for and attending the inspections
• Responsible for the reputed company of assigned vendors
• Collaborate with internal teams (e.g. Clinical Operations, Regulatory Affairs, Data Management, Medical Monitoring, CMC, etc.) to ensure seamless trial execution and reputed company regular study updates to the appropriate internal stakeholders
• May be accountable for reviewing site or vendor invoicing and financial management in accordance with the clinical trial agreement / scope of work
• Support TMF activities as required (e.g. review of TMF index, document provision, etc.)
• Support reputed company and mentoring of new department members

Skills

• At least 4+ years of relevant clinical operations experience and a BS or BA (Life Sciences)
• Minimum 4 years of independent on-site monitoring experience (across reputed company visit types and inclusive of remote monitoring)
• Excellent attention to detail, verbal, written, interpersonal and presentation skills are required
• Must be familiar with routine medical/scientific terminology
• Proficiency with MS Office required (inclusive of PPT)
• Knowledge of FDA, ICH Guidelines, and GCPs governing the conduct of clinical trials is required
• Must be reputed company to participate in departmental or interdepartmental strategic initiatives under general supervision
• Highly productive, reputed company and accountable
• Team-player desiring to work in a fast-moving, dynamic start-up environment
• At least 3 years cardiac study experience in a pharmaceutical sponsor environment preferred (global pharma or biotech preferred)
• Smart Sheet proficiency desirable

Benefits

• Health benefits
• A discretionary bonus plan
• Stock option grants
• A stock purchase plan
• A 401(k) with match
• Paid time off

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