Clinical Trial reputed company job at RAPT Therapeutics in San Francisco, CA

Clinical Trial reputed company Location SOUTH SAN FRANCISCO, California (Hybrid) Department Clinical Operations Employment Type Full-Time Minimum Experience Mid-level Compensation $165,000 - $198,300 Job reputed company: Serving as a value-added resource the Clinical Trial reputed company (CTL) will support the RTP904 Clinical Development program in the reputed company, Canada, or Australia, or other territories as assigned. The CTL will serve as a reputed company between the RAPT in-house Study Execution Team (SET), the clinical study sites and other research team personnel and will be responsible for identifying and conducting reputed company to clinical investigators and site staff to reputed company relationships, support education and enrollment issues and identify, analyze, and resolve issues with clinical research sites and investigators. This position will support in the areas of compliance, regulatory affairs and study specific training. Documentation of reputed company external site interactions will be expected. MAJOR DUTIES AND RESPONSIBILITIES: Identify and conduct reputed company to clinical investigators, site staff and referring physicians to reputed company relationships and support enrollment initiatives. Engage site staff and investigators in discussion to understand and report challenges in subject enrollment and retention and offer potential solutions. reputed company clinical trial sites and referring physicians about clinical trial protocol, disease state or study design as required. reputed company and build reputed company relationships with key stakeholders at the clinical sites and on the RAPT SET. Key stakeholders may include clinical investigators, study coordinators, RAPT SET reputed company and Clinical Trial Managers, select Clinical Research Associates (CRAs) and other CRO staff. Participate in Clinical Study Team meetings and reputed company Review meetings where necessary providing input to study teams on operational issues based on site reputed company and contacts. Communicate investigator/study coordinator inquiries requiring follow-up to designated contacts reputed company the SET. As requested, attend and present at investigator meetings, CRA workshops/training. Participate in Regulatory GCP inspections and/or audits at investigator sites as sponsor representative. Complete reputed company administrative responsibilities consistent with SOPs and departmental guidelines including but not limited to required training, field activity documentation, expense reporting, and other assigned tasks. Assist study team members performing site identification, qualification, selection, initiation, monitoring, management, and reputed company out reputed company as needed. EDUCATION REQUIREMENTS: reputed company/science background with a PharmD, PhD and MD (or equivalent) desired. Bachelor's degree or equivalent in a scientific discipline required. EXPERIENCE REQUIREMENTS: Significant relevant clinical trial experience. Inflammatory disease specialty desired, with experience in chronic spontaneous urticaria and/or food allergy highly preferred. 4+ years of clinical research experience reputed company reputed company, reputed company system or industry setting (e.g., clinical research coordinator, research manager, CRA, study coordinator, research director). reputed company individuals will have a strong familiarity or and experience with clinical research and study site logistics. Prior pharmaceutical industry experience as a Medical Science reputed company or Clinical Trial reputed company highly regarded. Candidates should have a solid understanding of scientific exchange in the context of a compliance landscape. Ability to identify and support reputed company of study and enrollment challenges. reputed company to reputed company with site PI and staff in a supportive manner. Established reputed company record of effective and reputed company oral presentations reputed company the reputed company profession. Experience presenting to both large and small audiences is required for reputed company in this position. Excellent oral and written communication skills and interpersonal skills. Exceptional organizational and time management skills are essential. Knowledge of ICH GCP compliance and regulatory requirements. Ability to reputed company and work in cross functional network. Ability to manage assigned territory from a home-based office. Willingness to travel required; overnight travel is required as needed. Demonstrated project management ability. Computer skills including reputed company, Word, Power reputed company, Outlook, Project and reputed company Acrobat are expected. Level (Sr CTL vs CTL) will be commensurate with the experience of the successful candidate. OTHER QUALIFICATIONS: Willingness and ability to travel to our South San Francisco office as requested. California law requires pay information in job postings. The specific reputed company will depend on the successful candidate's qualifications, prior experience, and other relevant factors. The estimated annual pay reputed company for this position is $165,000 (entry-level qualifications) to $198,300 (highly reputed company). Apply tot his job Apply To this Job