Regulatory Coordinator Salary at Tarte Inc BETA

Civil Engineer Project Manager Experience Level: 5-9 years | Location: Mason, OH Position Responsibilities: • Project management including guiding clients through all phases of project delivery (planning, scheduling, estimating, design, finance, and client management) • Developing designing and peer review of project construction document plans and specifications • Regulatory coordination, permitting and attending public agency review evening meetings • Construction administration • Supervision of project technical staff Position Requirements: • B.S. in civil engineering • At least 5 years experience in civil engineering site plan design consulting • Professional license in the state of Ohio Position Qualifications: • Strong electronic design skills (preferably Civil 3D) • Civil engineering design skills with a focus on site planning, grading, utility systems, stormwater management, sanitary sewer and water main design, and roadway improvements

Serves as an expert for FCCC research community on all regulatory matters related to the NCI Clinical Trials Support Unit (CTSU); including but not limited to Cancer Therapy Evaluation Program (CTEP) annual registration which is required for all persons participating in any NCI-sponsored clinical trial. Sr NCI Regulatory Coordinator is responsible for the accurate compilation and s, modifications and continuing reviews for protocols funded by the National Institute of Cancer (NCI). The Sr NCI Regulatory Coordinator is responsible to submit the materials described above to the FCCC Institutional Review Board (IRB), the Central Institutional Review Board for the National Cancer Institute (CIRB) or any other single IRBs reviewing trials funded by NCI within the currently define time period as outlined in the NCI audit guidelines. The Sr NCI Regulatory Coordinator will also assist the NCI Quality Assurance Auditor with tracking submissions timelines and in designing, improving and implemen

Position Details Position Details Job Title SR. REGULATORY COORDINATOR Position Number 8150786 Job Category University Staff Job Type Full-Time FLSA Status Exempt Campus Maywood-Health Sciences Campus Department Name CBCC Research Location Code HEMATOLOGY - ONCOLOGY (06508A) Is this split and/or fully grant funded? Yes Duties and Responsibilities Stays current with Federal regulations and can apply knowledge to work related activities. Has working knowledge of regulations pertaining to retention of records, protection of human subjects, IRB, FDA, and other regulations governing clinical research. Communicates with the CCTO Study Teams and Disease programs distributing new NCTN Study activations, closures, termination, amendments and safety reports, etc. Submits new Study projects to the local IRB, Central IRBs including- Cancer Trials Support Unit (CTSU), National Marrow Donor Program (NMDP) and Central Institutional Review Board (CIRB). Completes and tracks IRB submissions including a

Job Type Full-time Description Clinical research study point of contact and accountable for coordination of each assigned trial from beginning to the end under the direction of the Principal Investigator, Sub-investigator, and Clinical Trial Management in adherence to the FDA, ICH-GCP, IRB, HIPAA, RCCA SOPs, US Oncology Compliance Program, RCCA Code of Ethics and Business Standards. Employment Type: Full Time Location: Riverdale, NJ As of the date of this posting, RCCA offers a comprehensive benefits package for this position, subject to eligibility requirements. In addition to the salary, we provide: Health, dental, and vision plans, Wellness program, Health savings account - Flexible spending accounts, 401(k) retirement plan, Life insurance, Short-term disability insurance, Long-term disability insurance, Employee Assistance Program (EAP), Paid Time Off (PTO) and holiday pay, Tuition discounts with numerous universities, Employee-paid critical illness and accident insurance. We belie

POSITION SUMMARY: The Regulatory Coordinator provides administrative support with regulatory compliance matters including but not limited to maintaining compliance documentation and electronic filing system for regulatory records, collecting and entering data and assisting with regulator inspections. The incumbent is responsible for reviewing existing protocol, taking time to prepare approval submissions, filing regulatory documents, implementing improvements as needed, and following regulations regarding researcher, assessment, and data gathering accurately. PRINCIPLE RESPONSIBILITIES: In collaboration with the Regulatory leadership, formats regulatory submissions for electronic submission to regulatory authorities. Submits applications and related documents under the supervision of the Regulatory management. Facilitates responses to queries from the vendor assigned to submit applications to regulatory authorities. Assists in the tracking and filing of documents associated with regula

Job Type Full-time Description Regional Cancer Care Associates (RCCA) is looking for an exceptional Research Coordinator. This position is the study point of contact and accountable for coordination of each assigned trial from beginning to the end under the direction of the Principal Investigator, Sub-investigator, and Clinical Trial Management in adherence to the FDA, ICH-GCP, IRB, HIPAA, RCCA SOPs, US Oncology Compliance Program, RCCA Code of Ethics and Business Standards. This individual must also possess strong multi-tasking abilities and bring positivity and passion to their work. If you want to join a team that is on the cutting edge of cancer care, while always putting the patient first, we want to hear from you! While some experience is preferred, we are very open to new grads looking to explore oncology care. Employment Type: Full Time Location: Freehold, NJ As of the date of this posting, RCCA offers a comprehensive benefits package for this position, subject to eligibility r

Job Title: Regulatory Coordinator Location: Los Angeles, CA (Headquarters) – Up to 25% travel required to other clinical trial sites across California, Texas, Nevada, Washington, D.C., and additional locations. Pay: $24.03 - $48.87 Overview: A growing clinical research organization is seeking a detail-oriented and experienced Regulatory Coordinator to support and manage regulatory compliance across multiple clinical trial sites. This role plays a vital part in the success of ongoing studies and involves close collaboration with internal teams, sponsors/CROs, and regulatory agencies to ensure alignment with all relevant regulations and protocols. Travel to various research sites will be required to provide regulatory support as needed. Key Responsibilities: Prepare, submit, and maintain regulatory documentation for IRB and sponsor submissions across multiple clinical studies Ensure study documentation complies with GCP, FDA regulations, and institutional policies Maintain regulatory bin

Water Resources Engineer/Designer Location: Charlotte, NC Salary Range: $75,000-$115,000 (Based on education & experience) Summary A full-service engineering firm in Charlotte, North Carolina, is seeking a Water Resources Engineer/Designer to join our team. The ideal candidate will have a strong background in stormwater drainage planning, research, modeling, and design. This position offers the opportunity to work on impactful projects, collaborate with a dynamic team, and grow within a reputable firm. Key Responsibilities: Plan, design, and develop stormwater drainage solutions for roadway and street projects. Conduct research, modeling, and analysis to support project planning and execution. Utilize AutoCAD Civil 3D for design and drafting. Collaborate with project managers, engineers, and stakeholders to ensure compliance with regulatory requirements. Prepare reports, calculations, and project documentation. Assist with permitting and regulatory coordination. Qualifications: Bachelo