Top 2258 Global pharmaceutical Jobs in Remote

Associate, Global Compliance External Engagement
Daiichi Sankyo —Basking Ridge, NJ
- $30 - $38 an hour
- Part-time
- Remote
- Sales
- Customer service
- Bachelor of Science
- Dental insurance
- 401(k)
Global Technical Consultant Corporate Accounts - Life Sciences
Ecolab Inc. —Baltimore, MD
- $128,600 - $193,000 a year
- Overtime
- Remote
- Up to 50% travel
- 5 years
- Bachelor of Science
- Opportunities for advancement
Manager, Customer Analytics & Insights
Jazz Pharmaceuticals —San Diego, CA
- $120,000 - $180,000 a year
- Remote
- SQL
- Bachelor's degree
- Continuous improvement
- Health insurance
- Dental insurance
4d
Associate Director, Global Medical & Promotional Regulatory Affairs
Jazz Pharmaceuticals —California
- $160,000 - $240,000 a year
- Remote
- Bachelor of Science
- Senior level
- Leadership
- Health insurance
- Dental insurance
6d
Global Pharmacovigilance Safety, Senior Manager- Obesity
Amgen —Remote
- $140,799.10 - $190,492.90 a year
- Doctoral degree
- Master's degree
- High school diploma or GED
- Disability insurance
- Health insurance
Senior Global Supplier Quality Professional II
Kindeva Drug Delivery Careers —Remote
- $104,000 - $137,800 a year
- Full-time
- Remote
- 8 years
- Project management
- Senior level
- Health insurance
- Dental insurance
Quick Apply
Associate Director, Clinical Quality Compliance
Biogen —Remote
- $148,000 - $204,000 a year
- Full-time
- Master's degree
- Analysis skills
- Bachelor's degree
- Paid parental leave
- Employee stock purchase plan
4d
Senior Manager, Global Quality Assurance
Medexus Pharma —Remote
- Remote
- Microsoft Excel
- Master's degree
- Analysis skills
Director, Global Transparency
MediSpend —Remote
- $150,000 - $200,000 a year
- Full-time
- Remote
- 5 years
- Bachelor's degree
- Product management
- Paid parental leave
- Health savings account
Quick Apply
Regulatory Affairs Consultant
Edison Scientific —Remote
- $200 - $400 an hour
- Contract
- Remote
- Psychiatry
- Bachelor's degree
- Senior level
- Commuter assistance
- Paid parental leave
Global Service Area Lead - CMC Development & Quality
ProductLife Group —Remote
- $200,000 - $240,000 a year
- 11+ years
- Master's degree
- Doctor of Philosophy
Associate Director Global Clinical Program
Amgen —Thousand Oaks, CA
- Remote
- Management
- Doctoral degree
- 3 years
- Disability insurance
- Health insurance
6h
Senior Clinical Research Associate (Remote - Field Based)
Novartis —Remote
- $108,500 - $201,500 a year
- Full-time
- Remote
- 3 years
- Bachelor's degree
- Continuous improvement
- Health insurance
- 401(k) matching
Associate Director, Project Management
CG Oncology Inc —Remote
- $175,000 - $195,000 a year
- Full-time
- Remote
- 8 years
- Bachelor's degree
- US work authorization
- Health savings account
- Disability insurance
Global Project Manager
Emmes Group —Rockville, MD
- Full-time
- Remote
- Supervising experience
- Bachelor's degree
- Contracts
- Health insurance
- 401(k)
2d
Head of Global Product Supply
Rezolute —Remote
- $290,000 - $340,000 a year
- Full-time
- Remote
- Up to 50% travel
- Bachelor of Science
- 11+ years
- Paid holidays
- Disability insurance
Quick Apply
Associate Director, Analytical Development
Avalyn Pharma —Remote
- $180,000 - $205,000 a year
- Master's degree
- 8 years
- Doctor of Philosophy
Quick Apply
Clinical Sample Manager
SAB —Remote
- $130,000 - $150,000 a year
- Full-time
- Microsoft Excel
- Bachelor's degree
- Travel
Quick Apply
Senior Manager Quality Compliance (Rare Disease)
Amgen —Remote
- $132,037.30 - $178,638.70 a year
- Remote
- 7 years
- Bachelor of Science
- Writing skills
- Disability insurance
- Health insurance
Senior Program Manager, Global Medical Affairs - Rare Disease & General Medicine
Amgen —Remote
- $137,340.45 - $185,813.55 a year
- Remote
- Doctoral degree
- Master's degree
- High school diploma or GED
- Disability insurance
- Health insurance

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global pharmaceutical jobs near remote

Associate, Global Compliance External Engagement

Daiichi Sankyo -
Basking Ridge, NJ

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Job Details

Part-time | Contract
$30 - $38 an hour

Benefits

Dental insurance
401(k)
Vision insurance

Qualifications

Committee work
Document review (document control)
Medical law
Sales
Customer service
Bachelor's degree in finance
Bachelor of Science
Data Retention (Data management)
Filing
Mid-level
Bachelor's degree in business administration
Finance
Records retention
Bachelor's degree
Compliance documentation
Business Administration
Bachelor's degree in accounting
Business
Process management
2 years
Accounting
Project stakeholder communication
Stakeholder relationship building
Stakeholder management

Full Job Description

Employment as a Contingent Worker aligns well with individuals seeking career flexibility and non-traditional work arrangements, while also being motivated to produce exceptional results in prominent roles. Magnit Direct Source is a service provided by Magnit Global that connects top-tier talent directly to an industry-leading company. Daiichi Sankyo, Inc. and Magnit Global, in collaboration, offer flexible contingent assignments across diverse projects creating opportunities for engaging work. As a Contingent Worker, you will not be employed Daiichi Sankyo, Inc. You will be employed by our Managed Service Provider, Magnit Global, which oversees the majority of our temporary contract recruitment.

Job Title: Associate, Global Compliance External Engagement

Job Schedule: This role is an average of 20 hours per week; the hours can increase depending on coverage for another individual. Candidate can work 100% remote; prefer to be EST based and the schedule will be 10AM-2PM EST - Monday-Friday.

The Associate, Global Compliance External Engagement is a fully dedicated global role—not a dual-hatted position—reporting directly to the Head of Global External Stakeholder Engagement. This position will be responsible for supporting the global Cross Border Engagement Review (CBER) process and will also serve as the initial reviewer for all US-led CBER submissions. This individual will partner with other members of the CBER process, including CBER Committee Reviewers, local/country-level approvers, and CBER Steering Committee members to coordinate the submission and review of Cross Border Engagements. Additionally, this role will consult with US-based employees prior to their submitting requests to CBER by providing recommendations to modify proposed cross border engagement submissions, as needed.

Key responsibilities include:

Independent management, organization and administration of the CBER process by conducting intake and distribution of all CBER requests in the Global CBER portal.
Ensuring that all CBER submissions are complete, qualify for CBER, and contain all required documentation prior to distribution to CBER Reviewers. Responsible for coordinating the review/input for all countries that are implicated in the CBER request. Interact directly and frequently with CBER Committee Reviewers, Local Country-level Reviewers, and Business Requestors to assist with questions related to the review of CBER submissions.
Independently provide explanations and details of requests to applicable committee members. Provide status updates to the Business Requestor upon their request.
Provide review-related input from Local Country-level Reviewers to all CBER Committee members for consideration in their assessment of the submission. Follow up on outstanding requests and communicate the final CBER Committee determination to the Business Requestor.
Conduct close-out of all submissions including ensuring that all necessary documentation has been obtained, is included in the electronic file and is maintained in accordance with record retention requirements.
Conduct independent initial review (“first line review”) of all planned CBER requests originating from DSI Business Requestors to determine if they (1) require CBER review and (2) if proposed engagements comply with applicable healthcare laws/regulations, internal policy and procedure requirements. Make decisions/provide feedback to the CBER requestors regarding actions to be taken on each request.
Responsible for flagging issues pertaining to anti-kickback, false claim, and transparency reporting laws/regulations for additional DSI Compliance or Legal Affairs review.
Provide customer support and assistance with customer questions related to the global CBER portal. This role is intended for a pharmaceutical compliance or legal affairs professional with experience managing complex processes, systems, and time-sensitive reviews. The position requires the ability to work independently, make sound decisions, and manage a high volume of high-risk reviews.
Qualifications:
Knowledge of U.S. healthcare rules, particularly as they relate to payments and engagements with HCPs, customers, and patients.
A minimum of one- two years of pharmaceutical industry experience is required, with a strong preference for experience in compliance, legal affairs, or policy.
Familiarity with laws or industry guidance governing interactions with healthcare professionals and/or knowledge of pharmaceutical marketing and sales activities.
Bachelor of Science degree (preferably in Business Administration, Finance, or Accounting) are also preferred.

Hourly Pay Rate Range (dependent on location, experience, expectation)

The pay range that Magnit reasonably expects to pay for this position is: $ 30- $38/hr

Benefits: Medical, Dental, Vision, 401K (provided minimum eligibility hours are met)

All qualified applicants will not be discriminated against and will receive consideration for employment without regard to protected veteran status, disability, race, color, religion, sex, age, sexual orientation, gender identity or national origin.

#REMOTE

QUALIFICATION/LICENSURE
Work Authorization : US Citizen
Preferred years of experience : 1 years
Travel required : No travel required
Shift timings :

Apply Now

Refine Your Search

global pharmaceutical jobs in remote

Associate, Global Compliance External Engagement

Global Technical Consultant Corporate Accounts - Life Sciences

Manager, Customer Analytics & Insights

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Global Pharmacovigilance Safety, Senior Manager- Obesity

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Associate Director, Clinical Quality Compliance

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Director, Global Transparency

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Global Service Area Lead - CMC Development & Quality

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Senior Clinical Research Associate (Remote - Field Based)

Associate Director, Project Management

Global Project Manager

Head of Global Product Supply

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Clinical Sample Manager

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Senior Program Manager, Global Medical Affairs - Rare Disease & General Medicine

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