BeOne Medicines

Cancer has no borders. Neither do we.

Regulatory Affairs Intern

ComplianceComplianceInternshipRemoteTeam 10,001+Since 2010H1B No SponsorCompany SiteLinkedIn

Location

United States

Posted

13 days ago

Salary

$27 / hour

Bachelor DegreeEnglish

Job Description

• Work on programs and strategies for compounds in multiple stages of development. • Gain experience and exposure in global drug development through an understanding of laws, guidance, and regulatory requirements for drugs and combination products. • Partner with other Global and Regional regulatory team members with diverse skills and experiences in building solutions for real-life business challenges through hands-on projects. • Collaborate with Global Regulatory Strategy team members in providing support for generating Global Regulatory Strategic Plans in the Breast and Lung portfolios. • Collaborate with the Diagnostic / CDx team to identify programs that have diagnostic needs and define ‘touch points’ with the Global Regulatory Teams. • Support the Global Portfolio Leads in determining timings for governance meetings based on the Clinical Development plans. • Participate in project teams, as determined by the supervisor

Job Requirements

  • Currently obtaining an undergraduate degree in the life sciences or other related degree
  • Proficient in Microsoft Office
  • Ability to communicate and write English clearly, concisely, and effectively
  • Well-organized, with an ability to prioritize tasks
  • Independently motivated, with good problem-solving ability
  • Excellent interpersonal skills; a team player.

Benefits

  • Medical
  • Dental
  • Vision
  • 401(k)
  • FSA/HSA
  • Life Insurance
  • Paid Time Off
  • Wellness

Related Categories

Related Job Pages

More Compliance Jobs

Operational & Clinical Compliance Coordinator (Remote)

LEARN Behavioral

A national organization dedicated to nurturing the potential of children and young adults with autism and special needs.

Compliance13 days ago
Full TimeRemoteTeam 1,001-5,000H1B No Sponsor

The coordinator supports organizational adherence to regulations and policies by assisting with data management, monitoring data integrity, preparing reports, and supporting audits. Responsibilities also include maintaining client records according to HIPAA and resolving routine issues.

Data ManagementAudit SupportReport PreparationHIPAAPolicy EnforcementAdministrative Support
United States
Full TimeRemoteTeam 501-1,000Since 2013H1B No Sponsor

This role serves as the analytical and reporting leader, owning the framework for monitoring internal operations and delegated entities to ensure regulatory alignment and accountability. The manager will be a hands-on contributor developing reports, dashboards, and analytics while also leading a team of analysts.

SQLPower BITableauData AnalyticsRegulatory ReportingMedicare AdvantageCMS AuditsKPI DevelopmentRoot Cause AnalysisHealthcare Data
United States
$130K - $195K / year

Operational & Clinical Compliance Coordinator

LEARN Behavioral

A national organization dedicated to nurturing the potential of children and young adults with autism and special needs.

Compliance13 days ago
Full TimeRemoteTeam 1,001-5,000H1B No Sponsor

Operational & Clinical Compliance Coordinator managing data and audit compliance

Arizona
$19 / hour

Regulatory Affairs Associate II Contractor

Assembly Biosciences, Inc.

Assembly Bio (NASDAQ: ASMB) is an ambitious biopharmaceutical company with cutting-edge therapeutic clinical candidates capable of improving the lives of millions living with chronic hepatitis B virus (HBV) infection around the world, and research and preclinical programs focused on the discovery of novel antivirals to treat devastating viral diseases, including HBV, hepatitis delta virus (HDV) and herpesviruses. We pride ourselves on creating a culture and work environment that is scientifically driven, ambitious, and collaborative. We encourage diversity of thought that leads to great innovation and are looking to add great people to our dynamic team who are driven to transform the lives of patients. We set our sights high—and pursue our goals with determination. Our unique organization stands ready to welcome talented, motivated individuals, who share our ambitions. As an equal opportunity employer, we are committed to diversity and inclusion and will not tolerate discrimination and harassment of any kind. All employment decisions are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, national, social or ethnic origin, sex (including pregnancy), age, physical, mental or sensory disability, HIV status, sexual orientation, gender identity and/or expression, marital, civil union or domestic partnership status, past or present military service, family medical history or genetic information, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. Information for Recruitment Agencies Assembly Bio does not accept from recruiters/agencies any unsolicited resumes, or any candidate information including blinded resumes and will not be responsible for any fees related to resumes or candidate information that is unsolicited. Please do not contact hiring managers or Assembly Bio employees directly with any information related to a resume or a candidate. We handle all recruiting through our internal Human Resources team, and we will reach out to you directly should we wish to engage in a search. Your willingness to comply with this will significantly impact any decision we may make about doing business with you. Location South San Francisco, California (Remote) Department 250 Regulatory & Quality Assurance Employment Type Contractor Compensation $48 - $58/hr

Compliance13 days ago
Full TimeRemoteTeam 51-200

This role primarily supports regulatory activities by tracking deliverables, maintaining document repositories like Veeva RIM/eTMF, and assisting with submission readiness and lifecycle management under supervision. Key tasks include performing document quality checks, supporting publishing activities, and coordinating with cross-functional teams for required submission materials.

United States
$48 - $58 / hour