Business Coordinator, Regulatory Affairs
1 day ago
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge.
Job Description About the role:The Plasma-Derived Therapies (PDT) R&D Organization is dedicated to bringing forward new plasma-derived therapies for patients with immunologic, hematologic, and other complex diseases.
Join Takeda as an experienced Business Coordinator where you will provide high-level comprehensive administrative support for the Plasma-derived Therapies Business Unit Head of Regulatory Affairs and Head of Plasma, CMC and Device.
You will also manage the scheduling of internal and external meetings, coordinating travel arrangements, preparing reports, budgets, and managing dashboards. As part of the Regulatory team in PDT, you will report to our Head of Regulatory Affairs and manage special projects, events, and operational matters as assigned by our leadership team.
How you will contribute:- Provides comprehensive administrative support to the Head of Regulatory Affairs and the Head of Plasma, CMC and Device.
- Provides project support to the PDT Regulatory Function.
- Manages the Head of Regulatory and Head of CMC calendars, schedules appointments, and coordinates meetings, ensuring all necessary resources are prepared in advance.
- Understands priority meetings; schedules last-minute meetings when necessary.
- Organizes face-to-face, virtual, and hybrid meetings.
- Is aware of meeting locations and travel time between virtual and in-office locations.
- Includes pre-reads and proper meeting materials in the invites.
- Assists in the preparation and coordination of materials for department meetings and other R&D related Massachusetts events.
- Facilitates leadership team meetings; ensures timely distribution of agenda; takes meeting notes; tracks action items.
- Prepares reports, presentations, dashboards, and other documents as requested by the leadership team.
- Arranges travel; completes expense reports in a timely manner.
- Manages specialty documents and correspondence with necessary confidentiality, including letters, reports, emails, presentations, memos, etc.
- Reviews documents and proofreads work for grammar and spelling, accuracy, consistency of terms, and completeness; ensures document text and graphics adhere to corporate and organization guidelines and standards.
- Uses appropriate tools for required work including Microsoft Outlook, Word, Excel, Teams, and PowerPoint to track, analyze, document, and report data.
- Interfaces and communicates with internal and external stakeholders; directs people to the appropriate resources.
- Researches solutions and responds to email and phone inquiries with minimal input from direct supervisor; interacts effectively with all levels of employees throughout the company; ensures that communications are timely, clear, and professional.
- Collaborates with Procurement team to prepare documentation for payment of vendors, consultants, and suppliers; submits documentation and enters request for payments into accounting system; approves transactions; responds to inquiries from accounts payable and payees.
- Collaborates with Finance team to track and update budget reports and forecasts.
- Initiates, develops, leads, and participates in improvement processes; actively participates in resulting process improvements.
- In collaboration with other administrative partners and business coordinators, organizes internal engagement events and supports the planning and implementation of leadership engagements across the organization.
- Provides administrative support to employee workstreams, including in relation to Career Development, Work Processes, and Wellness.
- Understands the structure of the organization and develops a strong network across departments; draws on network to answer questions, solve problems, and successfully execute responsibilities.
- Makes decisions with general management direction. While making decisions, exercises greater latitude based on extensive administrative experience and knowledge of Takeda’s operations, policies, and procedures.
- Effectively prioritizes, balances, and manages a variety of projects with differing deadlines to successful completion for the Head of Regulatory and leadership team.
- Demonstrates confidentiality in execution of all responsibilities.
- Performs other duties as required.
- High school diploma/GED required. Associates degree or bachelor’s degree preferred.
- Minimum 8 years of relevant work experience, or equivalent combination of training and experience. Some industry experience is preferred.
- Strong PC literacy with advanced skills in Microsoft Outlook, Word, Excel, PowerPoint. Comfortable working with web-based applications such as Microsoft SharePoint, Lists, and Planner.
- Excellent verbal and written communication skills.
At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.
Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.
This position is currently classified as "hybrid" in accordance with Takeda's Hybrid and Remote Work policy.
Takeda Compensation and Benefits SummaryWe understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices.
For Location: Boston, MA
U.S. Hourly Wage Range:
The estimated hourly wage range reflects an anticipated range for this position. The actual hourly wage offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job. The actual hourly wage offered will be in accordance with state or local minimum wage requirements for the job location.
U.S. based employees may be eligible for short-term incentives. U.S. based employees may be eligible to participate in medical, dental, vision insurance, a 401(k) plan and company match, short-term and long-term disability coverage, basic life insurance, a tuition reimbursement program, paid volunteer time off, company holidays, and well-being benefits, among others. U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation.
EEO StatementTakeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.
LocationsBoston, MA
Worker TypeEmployee
Worker Sub-TypeRegular
Time TypeFull time
Job Exempt
No
#J-18808-Ljbffr-
Business Coordinator, Regulatory Affairs
1 week ago
Boston, United States Takeda Pharmaceutical Company Ltd Full timeBy clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. Job...
-
Regulatory Affairs Manager
4 weeks ago
Boston, MA, United States Spencer Rigby Full timeSpencer Rigby has partnered with a global leader in the development of innovative In Vitro Diagnostic (IVD) solutions and medical device software (SaMD). Through the build of a new Digital Solutions business segment, we are hiring a Regulatory Affairs expert to spearhead the RA program for the next wave in digital technologies while also overseeing the...
-
Regulatory Affairs Coordinator
4 weeks ago
Frisco, TX, United States CornerStone Staffing Full timeRegulatory Affairs CoordinatorCity: FriscoState: TexasZip: 75034CornerStone Professional Placement has partnered with a reputable medical device manufacturing client seeking a Regulatory Affairs Coordinator. As the Regulatory Affairs Coordinator, you will be responsible for assisting the Regulatory Affairs team with gathering and organizing documents for...
-
Boston, MA, United States AstraZeneca Full timeDo you have expertise in, and passion for, Regulatory Affairs? Would you like to apply your expertise and channel the scientific capabilities in a company that follows the science and turns ideas into life-changing medicines? Then AstraZeneca might be the one for you! At AstraZeneca, we are using cell therapy to revolutionize the treatment of...
-
Director, Regulatory Affairs
6 days ago
Billerica, MA, United States Parexel International Corporation Full timeGreat opportunity to use your regulatory expertise and lead a truly exceptional team! As a Director, Regulatory Affairs, you will use your expertise to lead and mentor a team of high-performing Regulatory Affairs professionals; provide invaluable strategic, technical, and regulatory advice to help clients with their various innovative product applications;...
-
Regulatory Affairs Coordinator
1 day ago
Boston, MA, United States Massachusetts General Physicians’ Organization Full timeJob Description - Regulatory Affairs Coordinator - Cancer Center Protocol Office (3313936) General Summary: The Regulatory Affairs Coordinator (RAC) will work with investigators, study staff, Institutional Review Boards (IRB), clinical trial sponsors, and federal regulatory agencies to ensure that regulatory requirements are met for clinical trials. This...
-
Director of Regulatory Affairs
4 weeks ago
Boston, MA, United States Meet Full timePosition OverviewOur client, an innovative biopharma company, seeks a Director of Regulatory Affairs to drive regulatory strategy for their anti-infective portfolio through all development phases. This role involves co-leading a US NDA with a cross-functional project team and serving as the FDA liaison. Working remotely from the US with international teams,...
-
Director of Regulatory Affairs
4 weeks ago
Boston, MA, United States Meet Full timePosition OverviewOur client, an innovative biopharma company, seeks a Director of Regulatory Affairs to drive regulatory strategy for their anti-infective portfolio through all development phases. This role involves co-leading a US NDA with a cross-functional project team and serving as the FDA liaison. Working remotely from the US with international teams,...
-
Director of Pharmacovigilance
2 days ago
Boston, MA, United States Biolink360 Full timeDirector of Pharmacovigilance & Regulatory Affairs About the Company Our client is a market leader in diagnostic imaging agents, a global company with under 1000 employees, with HQ in Boston. The person hired will direct all global pharmacovigilance activities and safety reporting for all marketed products, and oversee internal work team activities, and...
-
Head of Regulatory Affairs-CMC
2 days ago
Boston, MA, United States Ironwood Pharmaceuticals Full timeIronwood Pharmaceuticals is a leading global gastrointestinal (GI) healthcare company on a mission to advance the treatment of GI diseases and redefine the standard of care for GI patients. We are pioneers in the development of LINZESS (linaclotide), the U.S. branded prescription market leader for adults with irritable bowel syndrome with constipation or...
-
Senior Regulatory Affairs Specialist
4 weeks ago
Boston, MA, United States Arevna Full timeOverview of the Role:The Senior Regulatory Specialist provides comprehensive regulatory expertise, supporting daily departmental operations and collaborating with the Manager of Regulatory Affairs to manage global medical device registrations. This role involves ensuring the department’s compliance with regulatory policies and managing both electronic and...
-
Vice President, Regulatory Affairs
24 hours ago
Boston, MA, United States Tango Therapeutics Full timeCompany Overview Tango Therapeutics is a biotechnologycompany dedicated to discovering novel drug targets and delivering the next generation of precision medicine for the treatment of cancer. Using an approach that starts and ends with patients, Tango leverages the genetic principle of synthetic lethality to discover and develop therapies that take aim at...
-
Boston, MA, United States MannKind Corp Full timeAt MannKind, our employees are our number one asset, and we continue to be a tight-knit community where each of us has a critical role in our success. Committed to diversity, at MannKind we depend on a rich blend of ideas, backgrounds, and working styles in our quest to change the world for the better.Position Summary: MannKind Corporation is currently...
-
Regulatory Affairs Consultant
2 weeks ago
Boston, Massachusetts, United States Capgemini Full timeRegulatory Affairs ConsultantCapgemini is seeking a highly skilled Regulatory Affairs Consultant to manage and optimize our regulatory information management processes using the Veeva Vault RIM platform. The ideal candidate will have a strong background in regulatory affairs, experience with Veeva solutions, and a deep understanding of compliance...
-
Regulatory Affairs Specialist
2 days ago
Nevada, IA, United States Course Advisor Full timeWhat You Need to Know About Regulatory Affairs Specialist Example of Regulatory Affairs Specialist Job: Coordinate and document internal regulatory processes, such as internal audits, inspections, license renewals, or registrations. May compile and prepare materials for submission to regulatory agencies. Regulatory Affairs Specialist Responsibilities...
-
Director, Regulatory Affairs
2 months ago
boston, United States Meet Full timeDirector of Regulatory Affairs (CRO)Remote Opportunity - Candidates must be based in CST or ESTMeet has partnered with a mid-sized CRO that is looking for a Director of Regulatory Affairs to join their team. This candidate will be overseeing all Regulatory Strategy projects for the organization across a wide variety of therapeutic areas and modalities. Key...
-
Director, Regulatory Affairs
2 months ago
Boston, United States Meet Full timeDirector of Regulatory Affairs (CRO)Remote Opportunity - Candidates must be based in CST or ESTMeet has partnered with a mid-sized CRO that is looking for a Director of Regulatory Affairs to join their team. This candidate will be overseeing all Regulatory Strategy projects for the organization across a wide variety of therapeutic areas and modalities. Key...
-
Director, Regulatory Affairs
1 month ago
boston, United States Meet Full timeDirector of Regulatory Affairs (CRO)Remote Opportunity - Candidates must be based in CST or ESTMeet has partnered with a mid-sized CRO that is looking for a Director of Regulatory Affairs to join their team. This candidate will be overseeing all Regulatory Strategy projects for the organization across a wide variety of therapeutic areas and modalities. Key...
-
Director, Regulatory Affairs
4 weeks ago
Boston, United States Meet Full timeDirector of Regulatory Affairs (CRO)Remote Opportunity - Candidates must be based in CST or ESTMeet has partnered with a mid-sized CRO that is looking for a Director of Regulatory Affairs to join their team. This candidate will be overseeing all Regulatory Strategy projects for the organization across a wide variety of therapeutic areas and modalities. Key...
-
Vice President Regulatory Affairs
24 hours ago
Boston, MA, United States Albion Rye Associates Full timeCompany Overview: Join a cutting-edge biotechnology company in Boston, committed to pioneering breakthrough therapies that address unmet medical needs. Our team is passionate about translating science into therapeutic solutions, and we are looking for a highly experienced Vice President of Regulatory Affairs to lead our regulatory strategy and guide us...