Senior CTM

Company Overview 

Boston Pharmaceuticals is a clinical-stage biopharmaceutical company. We are developing highly engineered targeted therapies for patients with serious liver diseases. Our lead investigational program, BOS-580, is a long-acting once-monthly FGF21 analogue being studied in a Phase 2 clinical trial for metabolic dysfunction-associated steatohepatitis (MASH), also known as non-alcoholic steatohepatitis (NASH). 

Position Summary: 

The Sr. Clinical Trial Manager will support in managing and progressing all clinical programs at Boston Pharmaceuticals.  The ideal candidate will be a highly adaptable and a proactive problem-solver with the ability to critically evaluate and manage timelines and key deliverables. 

Roles & Responsibilities: 

• Manage contract research organizations and other external vendors to support clinical studies and ensure compliance with Boston Pharmaceuticals quality systems 

• Independently manage study activities, including study monitoring and performance management activities, data collection and reporting, and providing support as needed to the team of field champions. 

• Provide input to both the CRO and internal clinical development plans for the study and ensure study team adherence to the plans. 

• Develop and manage study timelines and project and track study enrollment 

• Contribute to the development of study related documents (contracts, ICF(s), protocol(s), IB(s), etc.) 

• Prepare clinical study budgets, monitor budgets for variances and approve invoices 

• Address and escalate relevant operational issues to key stakeholders 

• Be aware of and be able to predict deviations, or potential non-compliance concerns (at a protocol level, site level, study level) and rapidly resolve or escalate appropriately 

• Facilitate internal/external meetings with key cross-functional teams 

Qualifications: 

• BA/BS and 5 years of experience with direct clinical trial management, including management of vendors and CROs.  Ex-US trial experience is required. 
  

• Working knowledge of GCP, ICH and relevant CFRs is required 

• Experience managing late-stage clinical trials is required

• Project management skills, effective communication (written and verbal), adaptability and self-motivation are required attributes 

• Strong time management skills; ability to prioritize multiple tasks efficiently  

• Experience integrating with cross-functional teams such as Regulatory, CMC, procurement, and/or finance preferred 

• Experience working with SmartSheets is a preferred 

• Resourceful and able to handle multiple and changing priorities 

• Ability to think creatively and independently and be proactive  

• Ability to understand the team’s objectives and motivated to reach them 

• Ability to exercise discretion when managing confidential information 

• Strong team player: demonstrated ability and willingness to work on a team, assist team members as needed and accomplish tasks required to achieve goals 

• Embraces and embodies Boston Pharmaceuticals’ corporate values: Commitment to Patients, Decisive Innovation, Purposeful Urgency, Passion for Excellence, One Team