Global Publicly Traded Pharmaceutical company is expanding.

The Senior Clinical Trials Manager / Clinical Trials Manager (CTM) is responsible for leading the execution of clinical studies on schedule and on budget. Senior CTM / CTM levels reflect the experience, skill level, and capacity to manage larger and/or more complex studies, projects or programs. Candidates should be located in MA as office is in Waltham and will require on-site presence from time to time. Responsibilities 

• Accountable for project related efforts for the delivery of studies or programs that are critical to a product’s clinical development, ensuring that they are completed on time, within budget and in compliance with SOPs, regulations and ICH/GCP guidelines.
• Supports external vendor selection and management process and  assists in the development of RFP’s and vendor oversight plans.
• Provide clinical leadership to CROs, other vendors, CRA team, and CTAs.
• Develop timelines and budgets for assigned studies/programs and is responsible for delivery to both quality and agreed timelines. 
• Project leadership of the cross-functional study team, including external team members, CROs and vendors.
• Plan, negotiate, and manage site budgets as well as facilitate site contracting process. 
• Develop and implement robust contingency and issue management plans to solve complex issues that impact study or program milestones. 
• May provide technical advice to team members. 
• Disseminate clinical program communications to all functional groups and leads program, study and team meetings. 
• Interact with clinical research investigators, Key Opinion Leaders and sites. 
• Interact with Senior Management to report on progress of milestones. 
• Oversight of study team and site training 
• Facilitation of Quality processes and Quality Assurance interactions for assigned project(s) 
• Management of study drug distribution and accountability processes and documentation 
• Oversight of study start-up, study management, data cleaning, and study closeout activities 
• Responsible for final study files and documentation, including TMF, final TLFs, and final study data archival 
• Provides mentorship, review, assistance or leadership for the development and writing of study protocols, study plans, CRFs, informed consent forms.

Requirements

• BA/BS degree in Health or Life Sciences required, advanced degree preferred 
• A minimum 5+ years of experience or demonstration of equivalent capability in a Clinical Trials Manager role 
• Exceptional communication and interpersonal skills
• Positive team orientated attitude      
• Must speak fluent English if it is their second language
• Advanced proficiency in Microsoft Office and Microsoft Project 
• Reliable, self-motivated, team player 
• Detail oriented with excellent organizational skills 
• Ability to effectively manage multiple tasks and competing priorities
• Creative problem solver 
• Ability to travel is required 

Company offers a flexible work environment. This position is a hybrid work model based out of our Waltham, MA office. 

Company offers a comprehensive benefits package including:

· Remote work with technology tools and infrastructure

· Competitive pay and stock options for all employees

· Medical, dental, and vision coverage with 100% of premiums paid by Company for employees and their eligible dependents

· Company paid insurance programs

· Short- and long-term disability coverage

· Life, Travel and AD&D

· 401(k) Company Match with immediate company vest

· Employee Stock Purchase plan