CrawlJobs Logo

Intern, Global Study Operations

biomarin.com Logo

BioMarin Pharmaceutical

Location Icon

Location:
United States

Category Icon

Job Type Icon

Contract Type:
Not provided

Salary Icon

Salary:

24.00 - 32.00 USD / Hour

Job Description:

The BioMarin Summer Internship Program will enable students to gain valuable experience and knowledge of the processes and systems within BioMarin, while gaining an insight into the pharmaceutical/biotech industry. Over the course of 10 - 12 weeks our interns gain industry experience while working alongside our talented team on meaningful projects. The BioMarin Global Study Operations function is tasked with providing strategic direction on the feasibility, design, and conduct of clinical studies and drives the delivery of high-quality data to support the registration and approval of clinical development assets. The function achieves this through the development and operationalization of Clinical Development Plans, study planning and delivery, cross-functional leadership of Study Execution Teams, operational trial expertise, and vendor management and oversight.

Job Responsibility:

Support BioMarin’s Global Study Operations team in enhancing cross-functional understanding and internal capabilities through supporting the development of training materials, instructional videos, and resource toolkits

Requirements:

  • Undergraduate or Masters candidate enrolled in a life science, public health, communications, or related discipline
  • Strong interest in clinical research operations and digital learning
  • Excellent communication and organizational skills
  • High attention to detail, self-starter
  • Proficient in Microsoft 365 Applications (Outlook, SharePoint, PowerPoint, Excel, etc.)
  • Must be available to work full-time, 40 hours a week
  • Must be currently enrolled as a full-time student at an accredited U.S. based university or college and enrolled in the fall term after the completion of the internship OR have graduated within 1 year of the start of the program
  • Must be able to relocate if necessary and work at the designated site for the duration of the internship for on-site, hybrid roles. Some positions will be open to remote interns, but employee must be within United States borders

Nice to have:

  • Website maintenance
  • Video editing or eLearning model development
  • Administrative experience
What we offer:
  • Paid hourly wage, paid company holidays, and sick time
  • Apply skills and knowledge learned in the classroom to on-the-job experiences
  • Comprehensive, value-added project(s)
  • Develop skills specific to your major
  • Opportunities for professional development by building relationships and learning about other parts of the business
  • Participate in company all hands meetings, monthly community lunches
  • Corporate office amenities such as: 24/7 on-site gym, coffee truck, snacks
  • Access to Employee Resource Groups

Additional Information:

Job Posted:
December 26, 2025

Employment Type:
Fulltime
Work Type:
Remote work
Job Link Share:

Looking for more opportunities? Search for other job offers that match your skills and interests.

Briefcase Icon

Similar Jobs for Intern, Global Study Operations

Senior Study Specialist, Global Study Operations

The Sr. Study Specialist (SS) significantly contributes to or leads tasks relate...
Location
Location
United Kingdom , London
Salary
Salary:
Not provided
biomarin.com Logo
BioMarin Pharmaceutical
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • BA/BS or higher in nursing, life or health sciences is preferred
  • Industry or relevant experience in lieu of education is considered
  • Experience in a biotechnology or pharmaceutical company
  • Experience in oversight of external vendors including SOW, budgets, POs, and invoice management (e.g., CROs, central labs, imaging etc.)
  • Proficient knowledge and experience in Agility and Proactivity, Leadership, Communication and Collaboration, Study Management and Execution, Compliance and Quality, Drug Development and Study Design, Product and Therapeutic Area Knowledge
Job Responsibility
Job Responsibility
  • Develop study specific documentation, as delegated by the Study Manager
  • Contribute to the oversight of country and site feasibility assessment and site selection
  • Oversight of CRO for IRB/EC related submission/approval activities
  • Oversight of essential documents for study life-cycle management
  • Develop/Oversee site and investigator training materials
  • Present at investigator meetings as assigned
  • Ensure accurate and timely study entry and updates to ClinicalTrials.gov
  • Facilitate Screening Authorization Forms sign off and oversee tracking, where applicable
  • Process documents for signature in DocuSign
  • Oversight of Clinical Trial Insurance
Read More
Arrow Right

Local Study Associate Director

ICON plc is a world-leading healthcare intelligence and clinical research organi...
Location
Location
United States
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor degree in related discipline, preferably in life science, or equivalent qualification
  • Five years of US focused clinical trial management experience, including budget oversight
  • Good knowledge of international guidelines ICH- GCP as well as relevant local regulations
  • Excellent project management skill
  • Excellent team building and interpersonal skills
  • Excellent organisational skills
  • Excellent verbal and written communication skills
  • Excellent ability to prioritize and handle multiple tasks
  • Excellent attention to details
  • Excellent knowledge of spoken and written English
Job Responsibility
Job Responsibility
  • Has the overall responsibility for the study commitments within the country and for timely delivery of data to required quality
  • Leads and optimizes the performance of the Local Study Team(s) at country level ensuring compliance with Procedural Documents, ICH-GCP and local regulations
  • Ensures, as required, that clinical and operational feasibility assessment of potential studies is performed to the highest quality
  • Coordinates the site selection process by identifying potential sites/investigators, performing initial Site Quality Risk Assessment, and conducting Site Qualification Visits to evaluate suitability and quality risks
  • Ensures timely submission of application/documents to EC/IRB at start up and for the duration of the study
  • Works together with Regulatory Affairs to ensure timely delivery of application/documents for submissions to Regulatory Authority for the duration of the study, and in line with local regulations
  • Ensures timely preparation of country financial Study Management Agreement (fSMA) and maintains accurate study budget in AZ clinical studies financial system by regular checks of the system and financial reports (as agreed with Director, SMM/ Director, Country Head
  • Ensures timely preparation of local Master CSA (including site budget) and amendments as needed
  • Ensures timely preparation of country level Master Informed Consent Form (MICF) and subsequent site level ICFs, as required, including any relevant translations, and in line with relevant SOPs and local regulations
  • Ensures all country and site level trial essential documents required by ICH-GCP prior to study start have been collected and verified for correctness, prior to setting sites ready to enrol, and in line with SOPs
What we offer
What we offer
  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Read More
Arrow Right

Global Delivery Manager

ICON plc is a world-leading healthcare intelligence and clinical research organi...
Location
Location
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree in a scientific or related field
  • advanced degree preferred
  • Minimum of 5 years of experience in clinical research
  • 1-2 years working as an Associate Project Manager within a CRO or Pharma setting
  • Vendor management experience
  • Excellent knowledge of ICH-GCP, clinical study delivery process, including regulations, operational best practices, industry standards
  • Well familiar with key systems used in clinical trial delivery
  • Experience in using Trial Master File industry accepted standard
  • Strong project management skills (preferably with analytical / financial skills) and good leadership skills
  • Excellent verbal and written communication in English
Job Responsibility
Job Responsibility
  • Support the coordination and management of clinical trials
  • Contributing to the design, analysis, and advancement of innovative treatments and therapies
  • Delivering the clinical study to time, cost and quality
  • Ensuring inspection readiness by taking an oversight over study eTMF completeness
  • Working on end-to-end operational study delivery activities, from study setup to study archival
  • Setting up, maintaining and ensuring completeness of internal systems / databases / tracking tools and project plans (CSAP)
  • Working cross-functionally, with internal and external partners, on clinical study management activities
  • Monitoring study conduct and progress, identifying, resolving and escalating risks/issues
  • Reviewing key clinical documents, including the Protocol and Informed Consent Forms
  • Leading development of study plans (e.g. Monitoring Plan, Vendor Management Plan, Protocol Deviation Management Plan, Risk Management Plan, Communication Plan etc.)
What we offer
What we offer
  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments
Read More
Arrow Right

Study Delivery Senior Associate

The Study Delivery Senior Associate provides essential global study management s...
Location
Location
India , Hyderabad
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Master’s degree
  • Bachelor’s degree and 2 years of clinical execution experience
  • Associate’s degree and 6 years of clinical execution experience
  • High school diploma / GED and 8 years of clinical execution experience
  • 3 years’ work experience in life sciences or medically related field, including 1 year of biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company
  • Experience working on global clinical trials
  • Strong collaborative and effective communication skills within a team environment
  • Understands importance of accuracy in documentation, data tracking, and compliance checks
  • Expertise in clinical trial processes, operations, and oversight in biotech, pharmaceutical, or Contract Research Organization environments
  • Strong skills in using MS Word, Excel, PowerPoint, and other relevant software for documentation, data management, and trial support
Job Responsibility
Job Responsibility
  • Lead the development and maintenance of study-level trackers, dashboards, timelines, and tools
  • Coordinate logistics for investigator meetings, trial events, and site communications
  • Manage assigned start-up activities, including system setup, access management, and document readiness
  • Use study dashboards and reports to monitor global enrollment, data flow, and quality indicators
  • Lead delivery of assigned risk and quality management activities
  • Track and report study progress, coordinating with Study team and vendors to resolve operational issues
  • Deliver assigned components of global recruitment and retention strategies
  • Manage Study Training system activities and oversight
  • Build and maintain effective relationships with internal study team members, vendors and investigator sites
  • Act as a point of contact for routine study updates
What we offer
What we offer
  • Reasonable accommodation for individuals with disabilities
Read More
Arrow Right

Head of Customer Success – Brands & Agencies

We are seeking a senior leader to serve as Head of Customer Success for Global A...
Location
Location
United States , New York
Salary
Salary:
120000.00 - 135000.00 USD / Year
geniussports.com Logo
Genius Sports
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • 10+ years of experience in Customer Success, Account Management, or Client Services within Ad Tech, MarTech, or programmatic media
  • Extensive experience working directly with major global advertising agencies—ideally across multiple holding companies
  • Deep understanding of agency structures, decision-making processes, and media trading operations
  • Proven ability to build senior-level agency relationships and drive multi-market partnership growth
  • Strong understanding of programmatic workflows, data integrations, measurement, and cross-channel campaign execution
  • Exceptional executive communication skills, with an ability to influence senior stakeholders internally and externally
  • Demonstrated success in scaling global customer success teams and operations
Job Responsibility
Job Responsibility
  • Serve as the senior point of contact for Customer Success with major agency partners and top brand accounts
  • Collaborate with internal Sales teams to develop joint business plans (JBPs) and executive partnership programs to establish long-term, multi-market collaboration
  • Strengthen multi-level relationships—from global leadership to regional media directors and platform specialists
  • Champion the adoption of Genius Sports’s advertising capabilities and educate agency partners on how to integrate these capabilities into media plans, trading strategies, and testing frameworks
  • Develop the customer success vision and roadmap specifically for global agencies and their operating companies
  • Build frameworks that drive consistent product adoption across agency networks, regions, and business units
  • Align success initiatives with agency commercial goals, workflow models, and measurement requirements
  • Create scalable engagement models that support both enterprise-level relationships and in-market media teams
  • Lead onboarding, implementation, and activation programs tailored to agency workflows and media planning cycles
  • Build repeatable success plans that drive campaign performance, operational efficiency, and platform education across hundreds of client accounts throughout the sports calendar
What we offer
What we offer
  • variable compensation schemes
  • US benefits
  • 401k plans
  • Fulltime
Read More
Arrow Right

Study Delivery Senior Associate

The Study Delivery Senior Associate provides essential global study management s...
Location
Location
India , Hyderabad
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Master’s degree
  • Bachelor’s degree and 2 years of clinical execution experience
  • Associate’s degree and 6 years of clinical execution experience
  • High school diploma / GED and 8 years of clinical execution experience
  • 3 years’ work experience in life sciences or medically related field, including 1 year of biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company
  • Experience working on global clinical trials
  • Strong collaborative and effective communication skills within a team environment
  • Understands importance of accuracy in documentation, data tracking, and compliance checks
  • Expertise in clinical trial processes, operations, and oversight in biotech, pharmaceutical, or Contract Research Organization environments
  • Strong skills in using MS Word, Excel, PowerPoint, and other relevant software for documentation, data management, and trial support
Job Responsibility
Job Responsibility
  • Lead the development and maintenance of study-level trackers, dashboards, timelines, and tools
  • Coordinate logistics for investigator meetings, trial events, and site communications
  • Manage assigned start-up activities, including system setup, access management, and document readiness
  • Use study dashboards and reports to monitor global enrollment, data flow, and quality indicators
  • Lead delivery of assigned risk and quality management activities
  • Track and report study progress, coordinating with Study team and vendors to resolve operational issues
  • Deliver assigned components of global recruitment and retention strategies
  • Manage Study Training system activities and oversight
  • Build and maintain effective relationships with internal study team members, vendors and investigator sites
  • Act as a point of contact for routine study updates
Read More
Arrow Right

Study Delivery Senior Associate

The Study Delivery Senior Associate provides essential global study management s...
Location
Location
India , Hyderabad
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Master’s degree
  • Bachelor’s degree and 2 years of clinical execution experience
  • Associate’s degree and 6 years of clinical execution experience
  • High school diploma / GED and 8 years of clinical execution experience
  • 3 years’ work experience in life sciences or medically related field, including 1 year of biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company
  • Experience working on global clinical trials
  • Strong collaborative and effective communication skills within a team environment
  • Understands importance of accuracy in documentation, data tracking, and compliance checks
  • Expertise in clinical trial processes, operations, and oversight in biotech, pharmaceutical, or Contract Research Organization environments
  • Strong skills in using MS Word, Excel, PowerPoint, and other relevant software
Job Responsibility
Job Responsibility
  • Lead the development and maintenance of study-level trackers, dashboards, timelines, and tools
  • Coordinate logistics for investigator meetings, trial events, and site communications
  • Manage assigned start-up activities, including system setup, access management, and document readiness
  • Use study dashboards and reports to monitor global enrollment, data flow, and quality indicators
  • Lead delivery of assigned risk and quality management activities
  • Track and report study progress, coordinating with Study team and vendors to resolve operational issues
  • Deliver assigned components of global recruitment and retention strategies
  • Manage Study Training system activities and oversight
  • Build and maintain effective relationships with internal study team members, vendors and investigator sites
  • Act as a point of contact for routine study updates
Read More
Arrow Right
New

Executive Director, Study Start-Up

In this vital role as Executive Director, Study Start-Up (SSU), you will lead SS...
Location
Location
United States , Thousand Oaks
Salary
Salary:
281634.00 - 336501.00 USD / Year
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Doctorate degree and 6 years of clinical execution experience
  • Master’s degree and 10 years of clinical execution experience
  • Bachelor’s degree and 12 years of clinical execution experience
  • 6 years of managerial experience directly managing people and/or leadership experience leading teams, projects, programs or directing the allocation of resources
  • 12+ years’ work experience in life sciences industry, particularly focusing on clinical trial work, including 10+ years of biopharmaceutical clinical research experience obtained at a biotech or pharmaceutical company
  • Experience engaging and working across clinical trial teams in multiple geographies to deliver global clinical trials
  • Experience driving and leading organizations through cross-functional change initiatives such as identifying solutions to problems and innovating and change strategies and structure to meet future needs
  • Experience leading cross-functional / cross-geography / cross-trial teams, ensuring operational excellence and smooth decision-making
  • ability to escalate and resolve challenges in alignment with global study strategy priorities
  • Extensive knowledge of the clinical and pharmaceutical drug development process, from early to late-stage development with a deep understanding of relevant therapeutic areas to meet the highest scientific and regulatory standards
Job Responsibility
Job Responsibility
  • Shape the long-term vision and strategy of the SSU Hub, ensuring alignment with CPSO, GDO, and enterprise priorities
  • Integrate and harmonize strategies from the six sub-functions into a single global capability strategy, balancing standardization with local/regional adaptability
  • Act as the global escalation point for study start-up risks and issues, ensuring timely resolution and portfolio-level visibility
  • Embed within the industry - bringing outside ways of working and representing Amgen back into the industry
  • Build and develop a high-performing global SSU leadership team (Directors, Sr Managers) creating a culture of accountability, innovation and operational excellence
  • Lead, and mentor the global SSU Hub leadership team, ensuring robust succession planning, talent development, and organizational effectiveness
  • Drive consistent performance management, alignment, and calibration across sub-functions to ensure equitable resourcing and delivery
  • Embed a center of excellence mindset, encouraging knowledge-sharing and best practice adoption globally
  • Oversee start-up planning and execution across all new studies globally, ensuring timelines and quality standards are consistently achieved
  • Partner with Clinical Program Strategy and Operations TA Heads to ensure seamless integration of start-up into program execution
What we offer
What we offer
  • Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
  • A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
  • Stock-based long-term incentives
  • Award-winning time-off plans and bi-annual company-wide shutdowns
  • Flexible work models, including remote work arrangements, where possible
  • Fulltime
Read More
Arrow Right