Overview of salaries statistics of the profession "Project Coordinator in "

DescriptionAt Bath & Body Works, everyone belongs. We are committed to creating a diverse, equitable and inclusive culture focused on delivering exceptional fragrances and experiences to our customers. We focus on recruiting, retaining, and advancing diverse talent where our associate population is as diverse as the communities we serve, live and work. In addition, we work to improve our communities and our planet in a way that will make us proud for years to come because we believe the world is a brighter, happier place when everyone has access to the things that make them happy. We invite you to join Gingham Nation, where we invest in our associates through competitive compensation, benefits, and development opportunities, so they can continue to be their best at work, at home, and in their communities. As a Sales Support associate, you will have the opportunity to support delivering sales plan through selling effectiveness. Responsibilities Deliver a friendly and efficient cash wrap experience  Reinforce customer buying decisions at checkout Recover merchandise on the sales floor Replenish merchandise to brand standards Process merchandise to be sales floor ready and maintain the back room Assist with other projects as needed including floorset and shipment processing Abide by policies and procedures as advised Abide by Asset Protection and safety messages in daily operations QualificationsResponsibilities Deliver a friendly and efficient cash wrap experience  Reinforce customer buying decisions at checkout Recover merchandise on the sales floor Replenish merchandise to brand standards Process merchandise to be sales floor ready and maintain the back room Assist with other projects as needed including floorset and shipment processing Abide by policies and procedures as advised Abide by Asset Protection and safety messages in daily operations Core Competencies Lead with Curiosity & Humility Build High Performing Teams for Today & Tomorrow Influence & Inspire with Vision & Purpose Observe, Engage & Connect Strive to Achieve Operational Excellence Deliver Business Results The above statements are intended to describe the general nature and level of work being performed by people assigned to this job. They are not intended to be an exhaustive list of all responsibilities, duties and skills required. We will accommodate applicants and associates with disabilities in the recruitment, selection and assessment process as appropriate and as required by applicable law. Please call 855-556-2675 or email [email protected] if you require an accommodation. We are an equal opportunity and affirmative action employer. We do not make employment decisions based on an individual’s race, color, religion, gender, gender identity, national origin, citizenship, age, disability, sexual orientation, marital status, pregnancy, genetic information, protected veteran status or any other legally protected status, and we comply with all laws concerning nondiscriminatory employment practices. We are committed to providing reasonable accommodations for associates and job applicants with disabilities. Our management team is dedicated to ensuring fulfillment of this policy with respect to recruitment, hiring, placement, promotion, transfer, training, compensation, benefits, associate activities and general treatment during employment.  We only hire individuals authorized for employment in Canada.

Coordinator, Install & Project Sales (Full Time) Language English Français (CA) Apply Now By joining the RONA family, you’ll enjoy many benefits, such as: An inclusive and safe working environment Promotion of work-life balance Exclusive employee discounts Benefits: insurance (certain conditions apply), annual salary review, etc. Opportunities for advancement within the company An employer that’s involved in the community Teamwork and ongoing training A comprehensive training program for all new hires A student incentive program And much more! At RONA, over 22,000 employees let their passion blossom every day. Our teams from the RONA+, RONA, Réno-Dépôt, and Dick’s Lumber banners across Canada are driven by the desire to help people bring their projects to life and are committed to making a difference in the communities we serve.You’ve got the talent? We’ve got the tools! Here, your work and ideas will contribute to building a flourishing organization. Your voice will always be heard and valued. You’ll find career opportunities that live up to your ambitions and be able to further develop your unique set of skills. So if you’re looking to do what you love, we could be a perfect match.Your role : Build and develop professional relationships with customers; Liaison between customers and installers; Work with installers to provide customer quotes; Guide customers through their project; Perform administrative duties and reports; Be aware of current promotions and flyers; Comply with policies and procedures regarding loss prevention, breakage of goods and health and safety; Perform other duties as requested by the supervisor. The qualifications we are looking for:Do you have a knack for first-class customer service? Do you have general knowledge of building material and supplies? You have what it takes to be part of our team!RONA is committed to encouraging diversity and inclusion. We are pleased to consider applications from all qualified candidates, regardless of race, colour, religion, sexual orientation, gender, nationality, age, disability, or any other protected status. Apply Now

1. Provide coordination and direction in the development of data management methodologies and site management practices for multiple studies; including key data management methods.2. Preparation, design and/or support development of study specific documentation3. Perform site monitoring and site visits to confirm adherence to study protocol, procedures, ICH-GCP guidelines, local and national regulations and guidelines4. Evaluate and review high level study reports to confirm accuracy in data reporting for data monitoring and study committees5. Prepare and present reports; organize and facilitate data transfers with external stakeholders (both incoming and outgoing)6. Development and monitoring of study timelines and key deliverables in collaboration with internal and external stakeholders7. Management and administration of IP distribution, IP quality control and requirements per product monograph8. Mentor and support study staff by suggesting plans or training programs professional growth and development to aid team members in reaching their career goals9. Support Principal Investigator(s) in preparation of proposals, grant budgeting and writing as it pertains to human resources, investigator site payments, Investigational product, IT and system requirements10. Collaborate and provide guidance to supporting departments for the maintenance of study systems and development of study specific contracts11. Development and monitoring of study timelines and key deliverables in collaboration with internal and external stakeholders and project team members12. Other duties as assigned.

• Support Research Coordinator to oversee the operation and management of research projects. • Adhere to Good Clinical Practice and incorporate GCP requirements in all stages of research projects from start up to close up.  • Adhere to regulatory and local requirements (i.e. annual safety reports, periodic safety reports). • Adhere to timelines and milestones.  • Provide support to all collaborators (sites/countries) on a regular basis through communication. • Liaise with internal and external collaborators involved with research projects, to develop study agreements, complete regulatory/ethics submissions, and process payments for sites and other collaborators.  • Compile, review, and file essential documents • Help with training and orientation of study sites and staff.  • Help develop Manual of Operations and other study support tools, reports, and trackers. • Help create and test data reports, databases, audit case report forms (CRFs), and related programs • Help coordinate the process of transferring prepared study data to the study sponsor • Respond to data-related questions and query from internal and external partners • Coordinate logistics, review requirements, and confirm accuracy for the shipping and collection of materials and supplies for the main study as well as for sub-studies. • Prepare for meetings and teleconferences • Implement all study related amendments requested by the Principal Investigator • Help with publications and other study related documentations.  • Perform activities related to major protocol deviations  • Creation of data collection forms. • Regular communication with external parties  • Attend regular meetings prepare minutes and lines of actions. • Other working conditions may involve field work and irregular hours, such as weekend and evening work. • Enrolling participants via telephone, completing and tracking follow-up, medical chart reviews, and ongoing communication with project teams.  

• Support Research Coordinator to oversee the operation and management of research projects.• Adhere to Good Clinical Practice and incorporate GCP requirements in all stages of research projects from start up to close up. • Adhere to regulatory and local requirements (i.e. annual safety reports, periodic safety reports).• Adhere to timelines and milestones. • Provide support to all collaborators (sites/countries) on a regular basis through communication.• Liaise with internal and external collaborators involved with research projects, to develop study agreements, complete regulatory/ethics submissions, and process payments for sites and other collaborators. • Compile, review, and file essential documents.• Help with training and orientation of study sites and staff. • Help develop Manual of Operations and other study support tools, reports, and trackers.• Help create and test data reports, databases, audit  case report forms (CRFs), and related programs.• Help coordinate the process of transferring prepared study data to the study sponsor.• Respond to data-related questions and query from internal and external partners.• Coordinate logistics, review requirements, and confirm accuracy for the shipping and collection of materials and supplies for the main study as well as for sub-studies.• Prepare for meetings and teleconferences.• Implement all study related amendments requested by the Principal Investigator.• Respond to daily inquiries and facilitate communications on behalf of the central site. • Help with publications and other study related documentations. • Perform activities related to major protocol deviations. • Creation of data collection forms.• Regular communication with external parties. • Help provide training to staff. • Help provide training to external study staff.• Attend regular meetings prepare minutes and lines of actions.