Unfortunately, this job posting is expired.
Don't worry, we can still help! Below, please find related information to help you with your job search.
Some similar recruitments
Vendor Manager Jobs
Recruited by SSi People 8 months ago Address Waltham, MA, United States
Sr. Director Project & Process Management
Recruited by Staples 9 months ago Address Framingham, MA, United States
Sr. Manager, Program Management
Recruited by Chewy 9 months ago Address Boston, MA, United States
Marketing & Relationship Manager Jobs
Recruited by SecureBio 9 months ago Address Cambridge, MA, United States
Sr. Director, Talent Management
Recruited by Moderna 11 months ago Address Cambridge, MA, United States
Sr. Director, Product Management
Recruited by Aspen Aerogels 1 year ago Address Marlborough, MA, United States

Manager Clinical Outsourcing Jobs

Company

Blueprint Medicines

Address Cambridge, MA, United States
Employment type FULL_TIME
Salary
Category Biotechnology
Expires 2023-09-08
Posted at 9 months ago
Job Description
Blueprint Medicines is a global precision therapy company that invents life-changing therapies for people with cancer and hematologic disorders. Applying an approach that is both precise and agile, we create medicines that selectively target genetic drivers, with the goal of staying one step ahead across stages of disease. Since 2011, we have leveraged our research platform, including expertise in molecular targeting and world-class drug design capabilities, to rapidly and reproducibly translate science into a broad pipeline of precision therapies. Today, we are delivering approved medicines directly to patients in the United States and Europe, and we are globally advancing multiple programs for genomically defined cancers, systemic mastocytosis, and cancer immunotherapy.


Position Notes


  • Must have understanding of drug development.
  • Estimated contract duration is 11 months.


What will you do?


This position reports into the Director of Clinical Outsourcing. The right candidate will possess an understanding of Clinical Outsourcing activities for successful execution of multiple clinical trials primarily in oncology and hematology indications in various phases of development.


What will be your responsibilities?


Responsibilities of this position involve the day-to-day management of issuing Request For Proposals (RFPs), review of proposals, selection of key study vendors, and management of change orders for the company’s clinical trials in collaboration with a dynamic Clinical Development team.


  • Assists with benchmarking analysis
  • Leads the facilitation, management of governance meetings for key vendors as assigned
  • Supports he development of Outsourcing processes and tools
  • Leads the negotiation of rates and vendor discount opportunities with vendors as assigned
  • Collaborates effectively with all key functions including Clinical Operations, Finance, Legal, Biostatistics, PV, QA, Data Management, and Clinical Development to ensure appropriate stakeholder engagement in vendor selection and management.
  • Assists in maintaining a central database of contract tracking and delivery of metrics
  • Participates in pricing negotiations for CROs, Central Laboratories, Imaging, ePRO and other critical study vendors
  • Assists teams in the identification of potential vendors and CROs for clinical trial execution
  • Identifies and seeks efficiency in vendor contracting to ensure improved value for service
  • Leads the contracting activities including facilitating the review of MSA and amendments, development of Work Orders, Change Order notifications and Change Orders to ensure appropriate pricing and timely execution
  • Negotiates services descriptions, budgets, and payment schedules
  • Leads and facilitates cross functional review vendor selection meetings
  • Collaboratively creates and issues Request for Proposals (RFPs), compiles responses and facilitates team review of proposals from clinical trial vendors
  • Performs competitive bid analysis and derives recommendation to operational team leads


What basic qualifications do we require?


  • 2 + years in vendor and contract management with a sponsor company or CRO managing various phase clinical trials.
  • Minimum Education Required: bachelor’s degree in scientific or business discipline.


What additional qualifications are we seeking?


  • Strong interpersonal and organizational skills are needed, with a high degree of attention to detail
  • Experience in RFP procurement software a plus
  • Experience with vendor oversight
  • Creative problem solver with good communication and written skills
  • Experience in contracts, legal agreements, and financial budgeting preferred
  • Proficient with the MS Office Suite especially Excel
  • Ability to work with minimal direction
  • Experience with vendor selection (conducting RFPs, proposal review, and budget negotiations)
  • Commitment to Blueprint Medicines’ Core Values: Patients First, Thoughtfulness, Urgency, Trust, Optimism
  • Motivated self-starter who can work in a fast-paced environment
  • Understanding of the drug development process


Pay Transparency


The pay range that Magnit reasonably expects to pay for this position: $75.00-$100.00/hour. Benefits: Medical, Dental, Vision, 401K (provided minimum eligibility hours are met).


Requirement to Remain Up to Date with COVID-19 Vaccinations – Fully Vaccinated & Boosted


As a biotechnology organization, it is our responsibility to do everything we can to safeguard the health and safety of our workforce, our communities, and the patients we serve. That is why we require as a condition of initial and continuing employment that U.S. employees be fully vaccinated against COVID-19 and receive a booster when eligible. We will provide a reasonable accommodation due to a certified medical or religious contraindication if it does not present an undue hardship to Blueprint Medicines, consistent with applicable law. Accommodation requests for either of these reasons should be made to [email protected].


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 who requires an accommodation with the hiring process or to perform any essential functions of the position for which you are applying, please reach out to [email protected].


For more information, please see our EEO-AA-Policy-Statement, the EEO Poster and its Supplement, as well as our Pay Transparency Statement.


Who We Are


We don’t think in small steps. We think in giant leaps.


We are driven by the pursuit of new ideas, new innovations, and new ways of thinking.


We know that what each and every one of us matters and that our success depends on our ability to work together in a diverse community. We believe we are at our best as a company when our employees are thriving and we foster a culture that provides opportunities to grow and develop professionally, while also having fun.


]]>