Top 83 Document reviewer Jobs in Boston Ma

Associate Director, US Advertising & Promotion Regulatory Review
Takeda Pharmaceutical —Boston, MA
- $154,400 - $242,550 a year
- Full-time
- Remote
- 3 years
- Bachelor's degree
- Doctor of Philosophy
- Paid holidays
- Disability insurance
8d
Associate Director, US Advertising & Promotion Regulatory Review
Takeda Pharmaceutical —Boston, MA
- $154,400 - $242,550 a year
- Full-time
- Remote
- 3 years
- Bachelor's degree
- Doctor of Philosophy
- Paid holidays
- Disability insurance
1d
RN Reviewer
Cohere Health —Boston, MA
- $33 - $35 an hour
- Full-time
- Remote
- Google Workspace
- Nursing
- RN License
- Paid parental leave
- Health savings account
Quick Apply
Expedited Specialist
Mass General Brigham Incorporated —Somerville, MA
- $63,252.80 - $102,596.00 a year
- Full-time
- Remote
- Mid-level
- 3 years
- Master's degree
- Opportunities for advancement
Quick Apply
9d
Graduate Program Staff Assistant
Harvard University —Cambridge, MA
- Overtime
- Hybrid work
- Office
- 3 years
- University
- Commuter assistance
- Health insurance
1d
Client Coordinator
MES Solutions —Norwood, MA
- $17 an hour
- Full-time
- Remote
- Microsoft Excel
- Microsoft Outlook
- Medical office experience
- 401(k)
- Paid time off
Quick Apply
6d
English Contract Attorney
Contact Government Services, LLC —Boston, MA
- $27 - $40 an hour
- Contract
- Remote
- English
- Mid-level
- 2 years
Quick Apply
Attorney, Document Services
Zwicker & Associates, P.C. —Andover, MA
- $65,000 - $75,000 a year
- Full-time
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
- Paid holidays
- Disability insurance
Quick Apply
Clinical Reviewer, Physician Assistant
Cohere Health —Boston, MA
- $120,000 - $135,000 a year
- Mid-level
- 3 years
- Operating room
- Paid parental leave
- Health savings account
Quick Apply
Associate Director, Global Regulatory Affairs - Ad / Promo
BioNTech AG —Cambridge, MA
- $166,000 - $203,000 a year
- Full-time
- Background check
- Bachelor of Science
- 8 years
Technical Sales Support Engineer
Socomec, Inc. —Watertown, MA
- $90,000 a year
- Full-time
- Spanish
- Mid-level
- Office
- Health insurance
- Dental insurance
Quick Apply
9d
Executive Medical Director, Oncology Clinical Sciences
Takeda Pharmaceutical —Boston, MA
- $286,900 - $450,890 a year
- Full-time
- Medicine
- 7 years
- Office
- Paid holidays
- Disability insurance
Jr. Technical Sales Support Engineer
Socomec, Inc. —Watertown, MA
- $80,000 a year
- Full-time
- Hybrid work
- Spanish
- Engineering
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
9d
Facilities Engineer
Johnson Controls —Burlington, MA
- $76,100 - $114,100 a year
- Full-time
- OSHA
- 3 years
- Ability to lift 50 pounds
Quick Apply
5d
Sr. Statistical Programmer – Level 1
Clymb Clinical —Burlington, MA
- Full-time
- Computer Science
- Mid-level
- Office
Staff Regulatory Affairs Associate (Digital Health & AI Technologies)
WHOOP —Boston, MA
- $170,000 - $220,000 a year
- Full-time
- Computer Science
- Office
- 8 years
Director IRB Ops
Beth Israel Lahey Health —Boston, MA
- $155,002 - $184,995 a year
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Hospital
Manager, Medical Information
Sequel Med Tech —Marlborough, MA
- $75,000 - $140,000 a year
- Extended hours
- Hybrid work
- Nursing
- Medicine
- 5 years
- Health savings account
- Paid holidays
Director/Sr. Director Regulatory Labeling Strategy, Advertising, and Promotion, Regulatory
Agios Pharmaceuticals —Cambridge, MA
- $183,549 - $344,342 a year
- Remote
- 7 years
- Bachelor's degree
- Doctor of Philosophy
- Health insurance
Senior Loan Reviewer
Rockland Trust —Brockton, MA
- Office
- Finance
- Bachelor's degree
- Wellness program
- Health insurance

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Associate Director, US Advertising & Promotion Regulatory Review

Takeda Pharmaceutical -
Boston, MA

Apply Now

Job Details

Full-time
$154,400 - $242,550 a year
8 days ago

Benefits

Paid holidays
Disability insurance
Health insurance
Dental insurance
Tuition reimbursement
Paid time off
Vision insurance
401(k) matching
Volunteer time off
Life insurance

Qualifications

Drug regulation
Biomedical regulatory compliance
Regulatory submissions
Healthcare compliance
FDA regulations

Full Job Description

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:

Join Takeda as an Associate Director, US Advertising & Promotion Regulatory Review where you will be working on the US Medical team. In this role, you will be empowered to serve as an internal expert on FDA regulations, guidance, and enforcement trends governing the promotion of prescription drug and biologic products. You will contribute to Takeda’s mission by providing regulatory strategic oversight for complex products or therapeutic area products to help ensure regulatory compliance of promotional materials generated for assigned US products and/or compounds.

How you will contribute:

Be an internal expert on FDA regulations, guidance, and enforcement trends governing the promotion of prescription drug and biologic products.
Provide regulatory strategic oversight for at least one (1) complex product or therapeutic area/multiple products to help ensure regulatory compliance of promotional materials generated for assigned US products and/or compounds.
Interpret complex issues in relation to regulatory requirements and promotional strategy.
Mentor and develop staff. Supervise, train and provide technical and regulatory guidance to staff.
Be the chair of promotional review meetings and assist Commercial with the planning and prioritization of proposed promotional and disease state materials.
Collaborate with Regulatory Affairs, Medical, Legal, Commercial, and Compliance, execute and approve key Commercial campaigns. Provide expert guidance to help evaluate and mitigate potential risk.
Be an internal expert on FDA regulations, guidance, and enforcement trends governing the promotion of prescription drug and biologic products. Thoroughly review and assess proposed promotional items to evaluate their completeness, accuracy, and compliance with regulatory requirements.
Understand broad concepts within Regulatory Affairs and potential effects across the organization. Identify regulatory issues. Offer creative solutions and strategies, including risk mitigation strategies.
Provide product development and label development strategies to ensure promotional claims can be supported.
May provide management of individuals including mentoring, performance management, and staffing decisions. Identifies and proposes solutions to management for any resource gaps for brand responsibilities.
Present to senior management and cross-functional teams regarding shared insights from FDA advisory comments, recent enforcement actions, and/or guidance documents.
Be a primary liaison with OPDP and/or APLB reviewers in the request and negotiation of advisory comments and any other interactions regarding the use of claims for assigned business unit/therapeutic areas.

Minimum Requirements/Qualifications:

Bachelor’s Degree in life science or equivalent required. Advanced degree (PharmD, PhD, MS, MBA, JD) preferred.
You will have a minimum of 5 years’ experience in drug, biologic and/or device Regulatory Affairs or related field, including a minimum of 3 years’ experience specific to Regulatory Affairs – Advertising and Promotion.
Knowledge of applicable regulations and regulatory guidance specific to advertising and promotion of pharmaceutical/biologic products for healthcare professionals, payor and consumer audiences.
Experience in Regulatory Affairs promotion and advertising; experience managing major regulatory filing(s) (e.g., launch advisory comment submission or responses to enforcement letters) or competitor complaints.
Provide regulatory guidance to drug development teams, merging scientific principles and FDA law and regulations for development of marketing materials, including representation on global regulatory and labeling teams.
Provide leadership related to issues of importance; provide regulatory advice and recommendations involving regulatory issues on topics for which there may not be clear/specific regulatory insights.
Regulatory Affairs Certification (RAC) desirable

Takeda Compensation and Benefits Summary

We 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:

Massachusetts - Virtual

U.S. Base Salary Range:

$154,400.00 - $242,550.00

The estimated salary range reflects an anticipated range for this position. The actual base salary 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 base salary 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 and/ or long-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 Statement

Takeda 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.

Locations

Massachusetts - Virtual

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time

Job Exempt

Yes

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

#LI-Remote

Apply Now

Refine Your Search

document reviewer jobs in boston ma

Associate Director, US Advertising & Promotion Regulatory Review

Associate Director, US Advertising & Promotion Regulatory Review

RN Reviewer

Expedited Specialist

Graduate Program Staff Assistant

Client Coordinator

English Contract Attorney

Attorney, Document Services

Clinical Reviewer, Physician Assistant

Associate Director, Global Regulatory Affairs - Ad / Promo

Technical Sales Support Engineer

Executive Medical Director, Oncology Clinical Sciences

Jr. Technical Sales Support Engineer

Facilities Engineer

Sr. Statistical Programmer – Level 1

Staff Regulatory Affairs Associate (Digital Health & AI Technologies)

Director IRB Ops

Manager, Medical Information

Director/Sr. Director Regulatory Labeling Strategy, Advertising, and Promotion, Regulatory

Senior Loan Reviewer

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