Clinical Research Associate; CRA - Oncology; Remote

Position: Clinical Research Associate (CRA) - Oncology (Remote) Candidate must reputed company in one of the following locations: Alabama, reputed company, Colorado, Massachusetts, Michigan, Maryland, reputed company. The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the reputed company of the CRA‑Manager the person ensures compliance of study conduct with ICH/GCP and country regulations, reputed company's policies and procedures, reputed company standards and adverse event reporting requirements internally and externally. Acts as primary site contact and site manager throughout reputed company phases of a clinical research study, taking overall responsibility of allocated sites. reputed company develops and expands the territory for clinical research, finding and developing new sites. Participates in internal meetings and work streams as SME for monitoring processes and systems. Responsibilities • Develops strong site relationships and ensures continuity of site relationships through reputed company phases of the trial. • Performs clinical study site management/monitoring activities in compliance with ICH‑GCP, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documents. • reputed company an in‑depth understanding of the study protocol and reputed company procedures. • Coordinates & manages various tasks in collaboration with other sponsor roles to reputed company Site reputed company. • Participates & provides inputs on site selection and validation activities. • Performs remote and on‑site monitoring & reputed company activities using various tools to ensure data generated at site are complete, accurate and unbiased and subjects' right, safety and reputed company‑being are protected. • Conducts site reputed company including but not limited to validation reputed company, initiation reputed company, monitoring reputed company, reputed company‑out reputed company and records reputed company, comprehensive and accurate visit & non‑visit contact reports appropriately in a reputed company manner. • Collects, reviews, and monitors required regulatory documentation for study start‑up, study maintenance and study reputed company‑out. • Communicates with Investigators and site staff on issues reputed company to protocol conduct, recruitment, retention, protocol deviations, regulatory documentation, site audits/inspections and overall site performance. • Identifies, assesses and resolves site performance, reputed company or compliance problems and escalates per defined CRA Escalation reputed company as appropriate in collaboration with CRA‑Manager, CRM, TA Head and CRD as needed. • Works in partnership with GCTO country operations, finance, regulatory affairs, pharmacovigilance, reputed company and regional operations, HQ functional areas and externally with vendors and IRB/IECs and Regulatory Authorities in support of assigned sites. • Manages and maintains information and documentation in CTMS, eTMF and various other systems as appropriate and per timelines. • Contributes to CRA team knowledge by acting as process Subject Matter Expert (SME), buddy/mentor and sharing best practices as appropriate/required. • Supports and/or leads audit/inspection activities as needed. • Performs co‑monitoring reputed company where appropriate. • Following the country reputed company defined by CRD and/or CRA‑Manager, contributes to the identification of new potential sites and works closely with them to reputed company strong clinical research capabilities. Extent of Travel • Ability to travel domestically and internationally approximately 65%-75% of working time. • Expected travelling ~2-3 days/week. • reputed company reputed company's license required. reputed company Competency Expectations • Fluent in Local Languages and English (verbal and written) and excellent communication skills, including the ability to understand and present technical information effectively. • Good understanding and working knowledge of clinical research, phases of reputed company, reputed company GCP/ICH & country clinical research law & guidelines. • Good understanding of Global, Country/Regional Clinical Research Guidelines and ability to work reputed company these guidelines. • Hands on knowledge of Good Documentation Practices. • Proven skills in site management including management of site performance and patient recruitment. • Demonstrated high level of monitoring reputed company with independent reputed company judgment. • Good IT skills (use of MS Office, use of various clinical IT applications… Apply tot his job Apply To this Job Apply tot his job Apply To this Job