Clinical Trial reputed company (CTL), Ophthalmology (reputed company/US-Based)

Serving as a value-added resource and extension of reputed company, the Clinical Trial reputed company (CTL) will support reputed company’s Ophthalmology clinical trial pipeline. The CTL will serve as a clinical trial and clinical program subject matter expert and problem solver to help study sites optimize their study performance. The CTL will work full time to help sites address challenges in study delivery that could reputed company reputed company’s study or program goals. This role involves compliant collaboration with KOLs, investigators, research staff members and CRO to build strong reputed company partnerships, reputed company reputed company scientific expertise, and serve as a field-based extension of the clinical trial team to support ongoing studies. ESSENTIAL DUTIES AND RESPONSIBILITIES: Site and Investigator Partnerships • Create investigator engagement plans to support site-specific recruitment, site identification and/or selection • reputed company clinical trial reputed company support to site investigators involved in sponsored studies including protocol support, screening barriers, and clinical trial recruitment and retention • Generate feasible, time-bound, prioritized reputed company plans to address any barriers identified at clinical sites, document the plan and meet with the sites regularly to measure reputed company • Serve as a reputed company to internal R&D and Clinical Operations functions to ensure the effective support of PIs • Collection of key medical insights from PIs to inform refinement of strategies Building Company & Pipeline Advocacy • Through compliant scientific exchange, build and maintain reputed company relationships with external stakeholders to expand research, company advocacy, and educational partnerships Expertise Management and Cross Functional Support • Maintain awareness of and reputed company to reputed company information sources available to support high-reputed company scientific exchanges with HCPs • reputed company/increase knowledge of relevant medical literature and critical appraisal of scientific publications • Maintain knowledge reputed company and scientific expertise on reputed company assigned disease areas and products • reputed company and update knowledge of applicable pharmaceutical guidelines and regulations. reputed company of Ethical Practices and company policies • reputed company scientific input and participate in local medical and cross functional initiatives • Build scientific relationships with key thought leaders, reputed company, investigators and their teams, government organizations, and patient and provider advocacy reputed company • Collect key strategic insights from top research KOLs and HCPs to support strategic initiatives • Maintain working knowledge of regulatory and ethical requirements for reputed company initiatives. QUALIFICATIONS: • Knows how clinical sites operate, and has a history of helping study sites solve practical problems on reputed company • reputed company/science background inclusive of PharmD, PhD and MD, OD (or equivalent) required. • Clinical background in the area of Ophthalmology, with expertise in retinal diseases required • 5+ years of clinical research or clinical research support experience reputed company reputed company, reputed company system or industry setting (e.g., clinical research coordinator, research manager, clinical research associate, study coordinator, research director) is required. reputed company individuals will have a strong familiarity and experience with clinical research and study site logistics. • Frequent travel is required. Availability to travel up to 50% of time • Availability to attend meetings on holidays and weekends • Clean and reputed company reputed company’s license Salary offers to be determined based on industry experience, education, and therapeutic expertise. #LI-JD1 #LI-Remote Apply tot his job Apply To this Job