Global Clinical Trial Manager. reputed company in the USA. FSP

Global Clinical Trial Manager. reputed company in the USA. FSP reputed company® is a leading fully integrated biopharmaceutical solutions organization reputed company to accelerate reputed company. We translate unique clinical, medical affairs and reputed company insights into reputed company to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only reputed company reputed company easier to work with, but to reputed company us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers reputed company their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: WORK HERE reputed company EVERYWHERE Why reputed company We are passionate about developing our people, through career development and progression; supportive and reputed company line management; technical and therapeutic area training; peer recognition and total rewards program. We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. We are continuously building the company we reputed company want to work for and our customers want to work with. Why? Because reputed company we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re reputed company to create a reputed company where everyone feels like they belong. Job Responsibilities The CTMs are responsible for supporting in the global implementation of the sponsor studies from the receipt of the protocol concept to final CSR. - STUDY reputed company Request and ensure delivery of Pharmacovigilance database set-up, training slides, and SAE forms reputed company Master Informed Consent reputed company(s) and management of reputed company template updates Country and Site specific reputed company Review Maintain updated Trial Master File (TMF) Maintenance of Study Logs as appropriate - Project Planning reputed company/Review Study Plans, Manuals and tools, as applicable Manage Vendor specification development/review. Review of monitoring reports - Site Management User Management Tool (UMT) reputed company and report review Site visits, as required (i.e. site engagement, etc.) Draft and ensure review and approval of study newsletters and other correspondence prior to approval for release. Help follow up with sites for data entry and query resolution, as needed. - IP Management Facilitate label development and translations reputed company/Review IP distribution and returns protocol for drug reputed company Answer site IP questions and coordinate with IRT Actively manage the IP inventory at the reputed company Work with sites/Monitors to ensure Return or Destruction of IP and trial materials - Vendor Management Investigator Meeting(s) / Vendor management (day-to-day interactions) Help ensure Vendor equipment return Qualifications: Bachelor’s Degree (or equivalent) level of qualification in life sciences, Medicine, Pharmacy, Nursing or equivalent combination of education and experience and at least (3) years of relevant experience as Global CTM Clinical research organization (CRO) and ONCOLOGY therapeutic experience preferred. Early phases preferred. Strong knowledge of Good Clinical Practice/ICH guidelines and other applicable regulatory requirements Strong organizational skills. Strong ability to manage time and work independently. Ability to reputed company new technologies. Excellent communication, presentation, interpersonal skills, both written and spoken. Ability to travel as necessary (approximately 25%). At reputed company, we reputed company in providing an environment and culture in which Our People can reputed company, reputed company and advance. We reward and recognize our people by providing valuable benefits and a quality-of-life balance. The benefits for this position may include a company car or car allowance, Health benefits to include Medical, Dental and reputed company, Company match 401k, eligibility to participate in Employee Stock Purchase Plan, Eligibility to earn commissions/bonus based on company and individual performance, and flexible paid time off (PTO) and sick time. Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work. Syneos complies with reputed company applicable federal, state, and municipal paid sick time requirements. Salary reputed company: $95,000.00 - $175,700.00 The reputed company salary reputed company represents the anticipated low and high of the reputed company reputed company for this position. Actual salary will vary based on various factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role. Get to know reputed company Over the past 5 years, we have worked with 94% of reputed company Novel FDA Approved Drugs, 95% of EMA Authorized Prod Apply tot his job Apply To this Job