Clinical Research Site Manager
PPD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. At PPD, we are passionate, deliberate, and driven by our purpose- to improve health! Accelerated Enrollment Solutions (AES) is a business unit of PPD that helps biopharmaceutical companies overcome patient recruitment and research site challenges by optimizing each step in the patient journey to deliver greater speed, certainty, and control to clinical trial delivery. As a Site Manager you will be a key member impacting the development and research for therapeutics for patients. At PPD we hire the best, develop ourselves and each other, and recognize the power of being one team. We offer continued career advancement opportunities, award winning training and benefits focused on the health and well being of our employees. Summarized Purpose:
Manages the day to day activities, performance and supervision of the research site. Ensures execution of site protocols and providing daily direction to the site's staff. Acts as the liaison between the investigator and the research team and ensures the execution and coordination of clinical research activities according to the organization's SOPs, ICH/GCP and FDA guidelines. Supports the global aligned business objectives, growth, delivery of targets, quality management as well as the appropriate planning and coordinating of resources and facilities. Essential Functions and Other Job Information:
oManages staff, which may include interviewing and selection, job description preparation, professional development, goal setting, performance management, coaching and mentoring, employee counselling, and separations. Approves courses of action on salary administration, hiring, corrective action, and terminations. Reviews and approves time records, expense reports, requests for leave, and overtime. oManages site activities to ensure delivery of site targets as received from senior management. oProvides direct or indirect supervision of all clinical and administrative aspects of a clinical trial within the research site to ensure delivery of targets and quality. oResponsible for cost efficiencies within the site and all vendor contracts for services at the site. oContinuously oversees the schedules of site staff to ensure highest utilization of all resources. oEvaluates and implements new operational strategies to enhance efficiencies, provide competitive advantages, and improve overall profitability of the site. oMay provide input in the feasibility process, considering both recruitment and operational concerns. oCommunicates targets to the site teams and continuously measures progress. oPlans and prepares proactively for future studies according to new and defined strategies, embracing and implementing new TA area initiatives at the sites. oCollaborates with site and management regarding capacity planning and back-up plans, arranging and attending meetings. oEnsures patient recruitment activities are adequate for study requirements. oEnsures compliance with the company quality framework, regulatory (GCO) legislation, guidelines and international standards (Global/Local COPS/SOPS). #LI-JD1
Salary Range:
$100K -- $150K
Minimum Qualification
Healthcare ManagementEstimated Salary: $20 to $28 per hour based on qualifications.
Manages the day to day activities, performance and supervision of the research site. Ensures execution of site protocols and providing daily direction to the site's staff. Acts as the liaison between the investigator and the research team and ensures the execution and coordination of clinical research activities according to the organization's SOPs, ICH/GCP and FDA guidelines. Supports the global aligned business objectives, growth, delivery of targets, quality management as well as the appropriate planning and coordinating of resources and facilities. Essential Functions and Other Job Information:
oManages staff, which may include interviewing and selection, job description preparation, professional development, goal setting, performance management, coaching and mentoring, employee counselling, and separations. Approves courses of action on salary administration, hiring, corrective action, and terminations. Reviews and approves time records, expense reports, requests for leave, and overtime. oManages site activities to ensure delivery of site targets as received from senior management. oProvides direct or indirect supervision of all clinical and administrative aspects of a clinical trial within the research site to ensure delivery of targets and quality. oResponsible for cost efficiencies within the site and all vendor contracts for services at the site. oContinuously oversees the schedules of site staff to ensure highest utilization of all resources. oEvaluates and implements new operational strategies to enhance efficiencies, provide competitive advantages, and improve overall profitability of the site. oMay provide input in the feasibility process, considering both recruitment and operational concerns. oCommunicates targets to the site teams and continuously measures progress. oPlans and prepares proactively for future studies according to new and defined strategies, embracing and implementing new TA area initiatives at the sites. oCollaborates with site and management regarding capacity planning and back-up plans, arranging and attending meetings. oEnsures patient recruitment activities are adequate for study requirements. oEnsures compliance with the company quality framework, regulatory (GCO) legislation, guidelines and international standards (Global/Local COPS/SOPS). #LI-JD1
Salary Range:
$100K -- $150K
Minimum Qualification
Healthcare ManagementEstimated Salary: $20 to $28 per hour based on qualifications.
|
|
 | |
