Clinical Research Monitor Associate Salary at Synteract BETA

Job Description: We are seeking an experienced and highly motivated Clinical Trial Manager (CTM) with a strong background in respiratory clinical trials to join our growing clinical operations team. As a Clinical Trial Manager, you will play a key role in managing and overseeing the execution of clinical trials for respiratory therapies, ensuring that trials are conducted according to regulatory requirements, on time, and within budget. The ideal candidate will have hands-on experience in managing end-to-end clinical trial activities, with a strong understanding of the complexities and nuances of respiratory-focused studies. This is a great opportunity for a dedicated clinical professional to work in a dynamic biotech environment, driving innovative treatments in respiratory diseases and contributing to the future of healthcare. Key Responsibilities: Clinical Trial Management: Lead the planning, execution, and close-out of respiratory clinical trials, ensuring all milestones are achiev

Overview: Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites. At Velocity, we align our values and behaviors to give our employees the best chance of delivering on our brand promise: to bring innovative medical treatments to patients. We are committed to making clinical trials succeed by generating high quality data from as many patients as possible, as quickly as possible while providing exemplary patient care at every step. As an employee of Velocity, you are the most integral part of our mission. For talented candidates who perform at a high level, Velocity will invest to support career advancement and reward performance. Whether you are new to clinical research or are an industry veteran, we invite you to apply to Velocity. Benefits include medical, dental and vision insurance, paid time off and company holidays, 401(k) retirement plan with company-match, and a

Great permanent opening with Biotech specializing in Respiratory! Qualifications/ Responsibilities Lead global clinical trials from start up to close out Oversee and manage projects to ensure clinical trials are completed in a timely manner and within budget as agreed upon with the client Manage and coordinate all team activities to support delivery and execution of clinical trials Communicate project status and project reports with both internal and external stakeholders Manage the financial health of clinical study Run kick off meetings, investigator meetings, and team meetings Negotiate contracts, budgets, and timelines with sponsors, sites, and vendors Qualifications: Minimum 3+ years of Clinical Project Management experience in the clinical research industry Previous experience with Phases I-IV from start-up to close-out is highly preferred Knowledge of SOPs, ICH / GCP and local regulations CRO or Sponsor experience Strong Communication, Organizational, Management and Analytical s

Summary: We are looking for a Site Manager to support opening and operating a new facility in Hillsborough, NC. The ideal candidate will have previous experience managing clinical trial sites and clinical teams. Responsibilities: Oversee daily site operations, from start-up to ongoing management, ensuring compliance with established standard operating procedures. Collaborate closely with the Chief Operating Officer and the site’s Principal Investigator to align with organizational goals. Lead site team meetings, participate in management discussions, and ensure alignment with company culture and objectives. Continuously improve clinical processes and workflows to enhance efficiency and ensure compliance with study protocols and regulatory requirements. Manage and oversee site and study vendors, acting as a liaison between vendors and participants when necessary. Ensure availability and proper functioning of study supplies and equipment. Oversee site assessments, initiation visits, audi

Job Description Job Description Summary of The Position: The Oncology Therapeutic Lead is responsible for cultivating relationships with oncology stakeholders, assisting business development in developing an active oncology pipeline, and overseeing the successful execution of oncology clinical trials and research projects. This role involves strategic planning, execution, and delivery of oncology clinical studies, ensuring compliance with regulatory standards and achieving project milestones. Essential Functions: Provide therapeutic leadership, project oversight, and team guidance for assigned projects and client relationships across all phases of drug development. Provide executive oversight for oncology sponsor portfolios. Lead cross-functional clinical trial teams, ensuring effective collaboration and communication among team members. Assist with designing and reviewing oncology trial protocols, ensuring they meet regulatory requirements and scientific standards. Manage the executio

As a Principal Statistical Programmer you will be a key member of the Clinical Development Operations, Statistical Programming Team. You will p rogram routine and customized data displays, (including listings,?tables,?and graphics) in accordance with approved Statistical Analysis Plan and shell displays.?? Code is to be written using SAS, SAS procedures, or standardized macros.? You may assume a leadership role on a project, direct and/or mentor programmers at more junior levels and/or participate in department and/or company initiatives. Position Accountabilities/Responsibilities: + Creation of safety and efficacy SAS datasets.? + Creation of project specific macros and formats.? + Performing data checks as needed, to ensure integrity and correctness of data displays and to understand structure and content of?data.? + Perform QC/validation of datasets, tables, listings, figures to verify the?output.? + Establish, maintain, and strengthen a professional working relationship with client

Job Level: FSP Principal Biostatistician for Neuroscience Clinical Research Location: Home-based in the U.S. or Canada Why DSSS? Data Sciences Staffing Solutions, DSSS, is a unit within IQVIA that provides our sponsors with fully embedded resources through a Functional Service Provider (FSP) partnership. This means you get all the benefits of working for an industry leading global CRO while collaborating directly with expert cross-functional sponsor teams. Sponsor clients include world class pharmaceutical and biotech companies offering you unique opportunities to influence the future of medicine and advance therapies to market. Job Summary: The Principal Biostatistician is responsible for providing statistical support for novel neuroscience clinical research. Additional Benefits: Home-based remote working opportunities Work/life balance as well as flexible schedules. Collaborating with motivated, high-performance, statistical and research teams Technical training and tailored developm

Only Medical Doctors with the following specialties please apply: *Internal Medicine, Primary Care, Emergency Medicine, Neurology, Gastroenterology or Endocrinology This is a full-time or part-time position. Previous clinical research experience is preferred. Independent practice physicians are desirable. Company Description Eximia Research is a fully Integrated research sites network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology, medical device, pharmaceutical and clinical research organizations (CROs). Our premier, multidisciplinary wholly owned research sites located across country and known for excellent trial execution, rapid subject recruitment/enrollment and delivery of a quality data. Summary: The Principal Investigator responsibilities are centered around the execution, planning and management of assigned studies. Communicate succinctly with clients, study directors and technicians are key as is a cross-function