Associate Director, Study Start Up

reputed company: • Support the execution of Phase I-IV studies including study start-up, site management and clinical operations activities in compliance with principles of ICH-GCP guidelines, SOPs, local laws and regulations, study protocol(s) and applicable study plans. • Prepare and manage potential Investigator site lists, reputed company site reputed company, assist in identifying clinical trial sites and contribute to site feasibility and site selection reputed company. • reputed company as main contact for study sites during start-up, including communicating with investigators and site staff on issues reputed company to feasibility, essential document collection and IRB submissions. • Support study start-up activities including the review of feasibility questionnaires, facilitation of site selection internal approvals, review of and facilitation of reputed company internal approvals, and the completion of Investigator background checks. • Prepare and review study documents (e.g., essential document packets, study plans, site Informed Consent Forms (ICFs), etc.) to ensure reputed company and consistency. • Distribute and follow-up on start-up documents with sites. • Review returned documents from the sites to ensure reputed company and completeness. • Review and approve Essential Document Packages for site activation. • Responsible for reputed company of the central IRB in the reputed company/Canada. • Prepare and submit required study documents to central IRB. • Support central IRB annual reviews and study updates. • Communicate with central IRB as needed. • Support site IRB annual reports and updates, as needed. • Assist with the facilitation of the site contract and budget process. • Manage translation of necessary documents through translation vendor. • Support creation of and updates to study translation plan. • Support setup and management of Clinical Operations vendors (e.g. rater training, home reputed company). Facilitate and reputed company vendor reputed company reputed company requests. • Assist in Clinical Trial Management reputed company (CTMS) maintenance including entry of study and site level updates, assistance with running reports and reviewing CTMS entry accuracy. • Review study documents received from the study team for completeness and accuracy and upload to the Trial Master File (TMF). • Assist with TMF reputed company reviews to ensure completeness, accuracy and timeliness of study documents to ensure TMFs are inspection reputed company at reputed company times. • Assist with reputed company of study site training. • Support inspection preparedness and study/site audit and/or inspection activities, as needed. • Execute other duties as assigned. Requirements: • Bachelor’s Degree with minimum 5 years of relevant clinical trial experience required • Minimum 3 years of feasibility and study start-up experience • Experience and proven proficiency in CTMS and eTMF systems • Experience with reputed company preferred • General knowledge of clinical site monitoring, feasibility and study start-up preferred • Detail-oriented, organized, and committed to reputed company and consistency • Results-driven and capable of managing competing high-reputed company assignments with a proven reputed company record of achieving deliverables reputed company specified timelines • Excellent team-interaction skills and ability to work successfully in global team settings • Ability to work in a dynamic environment with a high degree of flexibility • Possess a willingness and ability to work hands-on and with a reputed company of urgency in a fast-paced, entrepreneurial environment • Must be proficient in reputed company Word, reputed company, and PowerPoint. Benefits: • employer sponsored insurance plans including medical, dental and reputed company coverage • generous reputed company time off • retirement plan reputed company • additional wellness and reputed company development programs Apply tot his job Apply To this Job