Global Study Manager Salary at Clincierge BETA

**Regional Drinking Water Process Leader-MID ATLANTIC REGION** Date: Oct 25, 2024 Location: Charlotte, NC, US Greenville, SC, US Orlando, FL, US US Company: Black & Veatch Family of Companies **Together, we own our company, our future, and our shared success.** As an employee-owned company, our people _are_ Black & Veatch. We put them at the center of everything we do and empower them to grow, explore new possibilities and use their diverse talents and perspectives to solve humanity's biggest challenges in an ever-evolving world. With over 100 years of innovation in sustainable infrastructure and our expertise in engineering, procurement, consulting and construction, together we are building a world of difference. **Company :** Black & Veatch Corporation **Req Id :** 105185 **Opportunity Type :** Staff **Relocation eligible :** Yes **Full time/Part time :** Full-Time **Project Only Hire :** No **Visa Sponsorship Available:** Yes **Why Black and Veatch** Recognized by Glassdoor as a 202

Summary/Job Purpose The Associate Medical Coding Director is responsible for the delivery of timely and quality coding deliverables for clinical trials and programs. This position develops and implements a long-term coding strategy to ensure that Exelixis meets industry and regulatory requirements for clinical trial coding. The Associate Medical Coding Director manages and oversees Exelixis staff, strategic partners, and vendors who conduct coding activities. They are responsible for conducting oversight of Data Management Coding activities at the portfolio, as performed by Exelixis coding specialists, CROs, or other 3rd Party Vendors, to ensure they meet deliverables per study timelines and comply with Exelixis coding conventions and procedures. This role is an onsite role that can be either located in Alameda, CA or King of Prussia, PA Essential Duties And Responsibilities Provides and enables solutions for complex problem solving that align with the Exelixis values. Establishes Prog

Job Description Job Description Job Title: Head of Regulatory Science Reports to (Title): CEO Location: Remote, US Exempt/Non-Exempt: Exempt Direct Reports : Yes Department: Regulatory Science EEO Job Category Professional Job Summary: This incumbent will be responsible for managing and leading all the regulatory activities including the communications with FDA and other regulatory agencies in ex-China regions. The incumbent will build strong Regulatory Science function to provide strategic assessment of the development pipeline and determine the regulatory path forward, to support product development by ensuring timelines of all regulatory deliverables and achieving marketing authorizations for Exegenesis Bio's development programs (as end goal). Essential Job Functions: Provide management and leadership to the Regulatory Affairs organization in the development and implementation of regulatory strategies and processes to gain product approvals worldwide Assist in clinical studies requ

Project Manager II, Delivery Lead Reports to: Manager, Services Delivery or Associate Director/Director/Senior Director, Services Delivery Department: Services Delivery Suvoda is a global clinical trial technology company shaping digital experiences that enable clinical trial sponsor and site professionals to take full command over the inherent logistical complexity behind mission-critical and time-sensitive patient interactions in life-sustaining studies for therapeutic areas such as oncology, central nervous system, and rare disease. Supporting clinical trials means supporting unique experiments that are inherently complex, high-stakes, and dynamic. It is imperative that Suvoda staff working with clients, end-users, or the systems that client and end-users interact with understand the clinical trial industry, regulations, Suvoda's software products and processes, and especially the specificities of the unique trial in question before taking any actions they may alter the data of the

Job Description This Vice President & Actuary position is responsible for leading and managing the actuarial staff in the Westchester Actuarial pricing unit for Casualty, Product Recall, Environmental and Programs. The role is based in Philadelphia, PA reporting to the Lead Actuary for Westchester and supports approximately $1.6B of annual GWP. Duties and Responsibilities related to this position: Work closely with WSG management to coordinate the actuarial support for Casualty, Product Recall, Environmental and Programs Supervise the actuarial pricing team including managing the staff's priorities, workloads, training and development in order to ensure timely delivery of: annual pricing studies, as well as ad-hoc pricing study requests monthly, quarterly and annual reporting requirements, including price monitoring and NvR, as well as the improvement of these reports as appropriate large account pricing referrals Work closely with the Finance team on the annual planning process, provi

**Company Description** **Work with Us. Change the World.** At AECOM, we're delivering a better world. Whether improving your commute, keeping the lights on, providing access to clean water, or transforming skylines, our work helps people and communities thrive. We are the world's trusted infrastructure consulting firm, partnering with clients to solve the worlds most complex challenges and build legacies for future generations. There has never been a better time to be at AECOM. With accelerating infrastructure investment worldwide, our services are in great demand. We invite you to bring your bold ideas and big dreams and become part of a global team of over 50,000 planners, designers, engineers, scientists, digital innovators, program and construction managers and other professionals delivering projects that create a positive and tangible impact around the world. We're one global team driven by our common purpose to deliver a better world. Join us. **Job Description** AECOMs Water Bu

The Senior Program Manager (EM&C Capital Infrastructure Improvements) has full technical responsibility for the interpretation, organization, execution and coordination of his/her assignments. He/She must have extensive knowledge of engineering, construction and business practices. A particular focus on cost engineering, engineering/design and construction methodologies is necessary. This position will have a dual function overseeing the planning design and construction phases of Capital Infrastructure projects plus the total project responsibility (conception to completion) of several major projects including the multiyear, multi-disciplinary programs e.g. Interlocking Programs, and Master Plans at various yards. The Senior Program Manager must come in contact with many people at higher organizational levels. These contacts may include the Board and General Manager, Assistant General Managers, Deputy General Managers, and Department Managers within the organization, as well as consult

Reporting directly to the VP of Regulatory Affairs (RA), the Director of Global RA will be responsible for providing US and global regulatory leadership in support of the development, registration, and life-cycle management of our innovative gene therapy programs. The responsibilities include providing US and global regulatory leadership and direction for gene therapy products, including developing long and short-term planning of regulatory projects that align with the company's business plan, and developing strategies to ensure effective achievement of regulatory/business objectives. The individual will be responsible for staying current in the regulatory environment and assessing and communicating the impact of changes on business and product development. The Director of RA will be an experienced and highly motivated professional who has developed regulatory strategy associated with all phases of drug development, including the coordination and preparation of document packages for re