What are the responsibilities and job description for the Late Phase Research Project Manager, Medical Affairs Operations position at Blueprint Medicines?
Blueprint Medicines is a global, fully integrated biopharmaceutical company that invents life-changing medicines. We seek to alleviate human suffering by solving important medical problems in two core focus areas: allergy/inflammation and oncology/hematology. Our approach begins by targeting the root causes of disease, using deep scientific knowledge in our core focus areas and drug discovery expertise across multiple therapeutic modalities. We have a proven track record of success with two approved medicines, including bringing our medicine to patients with systemic mastocytosis (SM) in the U.S. and Europe. Leveraging our established research, development, and commercial capability and infrastructure, we now aim to significantly scale our impact by advancing a broad pipeline of programs ranging from early science to advanced clinical trials in mast cell diseases including SM and chronic urticaria, breast cancer and other solid tumors.
Job Title: Late Phase Research Project Manager
Location: Cambridge, MA - Remote
We are seeking a highly experienced, organized, and motivated Clinical Study Manager (CSM) to join our dynamic Global Medical Affairs Operations team. This pivotal role will oversee late-phase, non-interventional studies and support the execution of medical affairs-driven research initiatives. Reporting to the Associate Director, Medical Program Management, the CSM will collaborate with Medical Strategy leadership, ensuring operational excellence in study management while contributing to broader medical affairs projects.
The ideal candidate will possess extensive expertise in late-phase study management and operational oversight, with a strong background in program/project management and cross-functional collaboration within the biotechnology or pharmaceutical industry.
Duties Include, But Are Not Limited To
Provide day-to-day operational oversight and management for late-phase, non-interventional studies, ensuring compliance with regulatory, ethical, and organizational standards.
Collaborate with cross-functional teams (medical, regulatory, legal, and compliance) to drive study progress, manage deliverables, and resolve operational challenges.
Develop and manage study timelines, budgets, and resource allocation, ensuring alignment with organizational goals.
Support protocol development, vendor selection and oversight, and study-specific operational plans.
Monitor study progress, generate status reports, and communicate key updates to stakeholders, ensuring proactive resolution of potential roadblocks.
Oversee the collection, review, and submission of study documents to ensure audit readiness and compliance with SOPs and regulatory requirements.
Partner with Medical Strategy leadership to identify and address strategic priorities in late-phase research, contributing to broader medical affairs initiatives.
Assist in the development and implementation of medical affairs processes, global planning templates, and operational best practices.
Support operational and project management activities for other key medical affairs initiatives, including advisory boards, medical education programs, and engagement activities.
5 years in clinical study management, with a focus on late-phase and non-interventional studies within biotechnology or pharmaceutical industries. Additional project management experience preferred.
Bachelor’s degree in Life Sciences, Pharmaceutical Sciences, or related field (advanced degree preferred).
Pay Transparency
The pay range that Magnit reasonably expects to pay for this position: $60.00 - 65.00 /hour.
Benefits: Medical, Dental, Vision, 401K (provided minimum eligibility hours are met).
Why Blueprint?
At Blueprint Medicines, we achieve impactful results because of our global crew of compassionate innovators – the Blue Crew. Through authentic relationships and our collective entrepreneurial spirit and action, we are each empowered to take ownership and execute with strategic prioritization. We put trust in our people to break through norms and conventions using their individual strengths and insights, which drives our success.
This is the place where the extraordinary becomes reality, and you could be part of it.
Patients are waiting. Are you ready to make the leap?
Equity, Diversity, Inclusion and Affirmative Action
At Blueprint Medicines, we foster a culture of equity, diversity, and inclusion. A proud Equal Employment Opportunity and Affirmative Action employer, we consider all qualified applicants without regard to race, color, sex, gender identity or expression, sexual orientation, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, or any other characteristic protected under applicable law. We are also an E-Verify Employer. We will make reasonable accommodations, absent undue hardship, for qualified individuals with known disabilities. If you are an individual with a disability in need of accommodation with the application or recruiting process, please reach out to TotalRewards@blueprintmedicines.com.
For more information, please see our EEO-AA Policy Statement, the EEO Know Your Rights Poster, as well as our Pay Transparency Statement.
Job Location: Cambridge, Massachusetts - Remote
Contract Duration: 10 months
Job Title: Late Phase Research Project Manager
Location: Cambridge, MA - Remote
We are seeking a highly experienced, organized, and motivated Clinical Study Manager (CSM) to join our dynamic Global Medical Affairs Operations team. This pivotal role will oversee late-phase, non-interventional studies and support the execution of medical affairs-driven research initiatives. Reporting to the Associate Director, Medical Program Management, the CSM will collaborate with Medical Strategy leadership, ensuring operational excellence in study management while contributing to broader medical affairs projects.
The ideal candidate will possess extensive expertise in late-phase study management and operational oversight, with a strong background in program/project management and cross-functional collaboration within the biotechnology or pharmaceutical industry.
Duties Include, But Are Not Limited To
Provide day-to-day operational oversight and management for late-phase, non-interventional studies, ensuring compliance with regulatory, ethical, and organizational standards.
Collaborate with cross-functional teams (medical, regulatory, legal, and compliance) to drive study progress, manage deliverables, and resolve operational challenges.
Develop and manage study timelines, budgets, and resource allocation, ensuring alignment with organizational goals.
Support protocol development, vendor selection and oversight, and study-specific operational plans.
Monitor study progress, generate status reports, and communicate key updates to stakeholders, ensuring proactive resolution of potential roadblocks.
Oversee the collection, review, and submission of study documents to ensure audit readiness and compliance with SOPs and regulatory requirements.
Partner with Medical Strategy leadership to identify and address strategic priorities in late-phase research, contributing to broader medical affairs initiatives.
Assist in the development and implementation of medical affairs processes, global planning templates, and operational best practices.
Support operational and project management activities for other key medical affairs initiatives, including advisory boards, medical education programs, and engagement activities.
5 years in clinical study management, with a focus on late-phase and non-interventional studies within biotechnology or pharmaceutical industries. Additional project management experience preferred.
Bachelor’s degree in Life Sciences, Pharmaceutical Sciences, or related field (advanced degree preferred).
Pay Transparency
The pay range that Magnit reasonably expects to pay for this position: $60.00 - 65.00 /hour.
Benefits: Medical, Dental, Vision, 401K (provided minimum eligibility hours are met).
Why Blueprint?
At Blueprint Medicines, we achieve impactful results because of our global crew of compassionate innovators – the Blue Crew. Through authentic relationships and our collective entrepreneurial spirit and action, we are each empowered to take ownership and execute with strategic prioritization. We put trust in our people to break through norms and conventions using their individual strengths and insights, which drives our success.
This is the place where the extraordinary becomes reality, and you could be part of it.
Patients are waiting. Are you ready to make the leap?
Equity, Diversity, Inclusion and Affirmative Action
At Blueprint Medicines, we foster a culture of equity, diversity, and inclusion. A proud Equal Employment Opportunity and Affirmative Action employer, we consider all qualified applicants without regard to race, color, sex, gender identity or expression, sexual orientation, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, or any other characteristic protected under applicable law. We are also an E-Verify Employer. We will make reasonable accommodations, absent undue hardship, for qualified individuals with known disabilities. If you are an individual with a disability in need of accommodation with the application or recruiting process, please reach out to TotalRewards@blueprintmedicines.com.
For more information, please see our EEO-AA Policy Statement, the EEO Know Your Rights Poster, as well as our Pay Transparency Statement.
Job Location: Cambridge, Massachusetts - Remote
Contract Duration: 10 months
- Work Authorization : Green Card, US Citizen
- Preferred years of experience : 5yrs
- Travel Required : No travel required
- Shift timings: Not specified
Salary : $60 - $65
