Boston Pharmaceuticals
Clinical Trial Associate
Boston Pharmaceuticals, Cambridge, Massachusetts, us, 02138
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). Our second investigational program, BOS-342, is a targeted immunotherapy currently being studied in a Phase 1 clinical trial for the treatment of liver cancer.
Position Summary:
The CTA will support in progressing all clinical programs at Boston Pharmaceuticals by managing a variety of administrative and operational responsibilities within Clinical Operations, including monitoring budgets and invoicing, taking meeting minutes, and monitoring reports from clinical sites. The ideal candidate will be a highly adaptable and a proactive problem-solver with the ability to balance multiple priorities and communicate clearly with all internal and external stakeholders.
Roles & Responsibilities:
* Participate in study team meetings, including compiling agenda items, recording meeting minutes and actions, distributing pre- and post-work to team members, and organizing/filing documents for future reference* Organize and maintain local study files and Trial Master Files for multiple studies* Support Clinical Operations in study management and vendor oversight activities, including reviewing essential documents, monitoring reports, and tracking metrics* Assist study teams with preparation of documentation and presentation materials* Assist with creation and maintenance of study timelines* Address and escalate relevant operational issues to key stakeholders as appropriate* Prepare clinical study budgets, monitor budgets for variances and approve invoices
Qualifications:
* BA/BS plus 1-2 years of clinical research experience required* Experience with clinical trial management systems (CTMS) and/or Trial Master Files (TMF) a plus* Excellent attention to detail and communication skills* Strong time management and organizational skills* Ability to exercise discretion when managing confidential information* Strong time management skills; resourceful, able to prioritize multiple tasks and changing priorities* Experience working with SmartSheets preferred* Proactive mindset; ability to understand the team's objectives and motivated to reach them* Embraces and embodies Boston Pharmaceuticals' corporate values: Commitment to Patients, Decisive Innovation, Purposeful Urgency, Passion for Excellence, One Team
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). Our second investigational program, BOS-342, is a targeted immunotherapy currently being studied in a Phase 1 clinical trial for the treatment of liver cancer.
Position Summary:
The CTA will support in progressing all clinical programs at Boston Pharmaceuticals by managing a variety of administrative and operational responsibilities within Clinical Operations, including monitoring budgets and invoicing, taking meeting minutes, and monitoring reports from clinical sites. The ideal candidate will be a highly adaptable and a proactive problem-solver with the ability to balance multiple priorities and communicate clearly with all internal and external stakeholders.
Roles & Responsibilities:
* Participate in study team meetings, including compiling agenda items, recording meeting minutes and actions, distributing pre- and post-work to team members, and organizing/filing documents for future reference* Organize and maintain local study files and Trial Master Files for multiple studies* Support Clinical Operations in study management and vendor oversight activities, including reviewing essential documents, monitoring reports, and tracking metrics* Assist study teams with preparation of documentation and presentation materials* Assist with creation and maintenance of study timelines* Address and escalate relevant operational issues to key stakeholders as appropriate* Prepare clinical study budgets, monitor budgets for variances and approve invoices
Qualifications:
* BA/BS plus 1-2 years of clinical research experience required* Experience with clinical trial management systems (CTMS) and/or Trial Master Files (TMF) a plus* Excellent attention to detail and communication skills* Strong time management and organizational skills* Ability to exercise discretion when managing confidential information* Strong time management skills; resourceful, able to prioritize multiple tasks and changing priorities* Experience working with SmartSheets preferred* Proactive mindset; ability to understand the team's objectives and motivated to reach them* Embraces and embodies Boston Pharmaceuticals' corporate values: Commitment to Patients, Decisive Innovation, Purposeful Urgency, Passion for Excellence, One Team