Associate Manager - Clinical Operations

Associate Manager - Clinical Operations #clinicalresearch #clinicaltrials #medicine #research #healthcare #medicalresearch #clinicaltrial #science #clinical #health #clinicalstudies #pharma #medical #pharmacy #biotech #covid #biopharma #pharmaceuticals #clinicalstudy #pharmacovigilance #medicalaffairs #clinicalresearchassociate #pharmaindustry #doctor #pharmaceuticalindustry #phd #oncology #drugdevelopment #cra #biotechnology Manage staff in accordance with organization s policies and applicable regulations. Responsibilities include planning, assigning, and directing work, assessing performance and guiding professional development, rewarding and disciplining employee, and addressing employee relations issues and resolving problems. Participate in the selection process for hiring new employees by conducting candidate review and participating in the interviewing process. Ensure that new employees are properly onboarded and trained. Ensure that staff has the proper materials, systems access and training to complete job responsibilities. Provide oversight for the execution of the training plan, SOP review and training experiences, as applicable. Participate in the allocation of resources to clinical research projects by assigning staff based on their experience and training. Manage the quality of assigned staff's clinical work through regular review and evaluation of work product. Identifies quality risks and issues and create appropriate corrective action plans to prevent or correct deficiencies in performance of staff. Ensures that staff are meeting defined workload and quality metrics through regular review and reporting of findings as outlined by clinical operations management. Qualifications Bachelor's Degree Degree in scientific discipline or health care preferred. Req Prior clinical trial experience or equivalent combination of education, training and experience. In-depth knowledge of applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines). Good leadership skills. Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint. Written and verbal communication skills including good command of English. Excellent organizational and problem solving skills. Effective time management skills and ability to manage competing priorities. Ability to establish and maintain effective working relationships with coworkers, managers, and clients. training and experience. In-depth knowledge of applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines). Good leadership skills.