CrawlJobs Logo

Intern, project manager, clinical development

biomarin.com Logo

BioMarin Pharmaceutical

Location Icon

Location:
United States , San Rafael

Category Icon
Category:
IT - Administration

Job Type Icon

Contract Type:
Not provided

Salary Icon

Salary:

24.00 - 27.00 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. As part of the BioMarin R&D Project Management Organization (PMO), the Intern Project Manager supports and drives the efficiency and effectiveness of cross-functional sub-teams in partnership with the Project Managers through meeting management, timeline development / management / tracking, and cross-functional communications. The PMO sits within BioMarin Research and Development (R&D), and the intern will have the opportunity to see a broad scope of drug development with the ability to interact with scientists and professionals across the organization.

Job Responsibility:

  • Work closely with the Clinical Development PM to propose a new structure and content plan for the PMO SharePoint site
  • Engage with representatives from each PMO branch to understand their roles and contributions to drug development
  • Gather and organize key resources and documentation to improve accessibility and transparency
  • Tracking project and program timelines, drive action item completion, and document decision making for CDTs
  • Scheduling clinically focused meetings, generate the agenda and facilitate the meeting (in collaboration with the team lead), and document/distribute minutes and action items
  • Identifying opportunities for standardization or process efficiencies based on cross-functional insights
  • Attend cross-functional team meetings and Production Integration Management Team (PRIME) team meetings to develop an understanding of clinical development

Requirements:

  • In progress bachelor’s degree in health or life sciences, including chemistry, molecular biology, or similar
  • 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

Nice to have:

  • Drug development and product knowledge
  • Team and stakeholder management and communication
  • Process improvement
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:
Hybrid 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, project manager, clinical development

Manager, Clinical Operations, International

Cabaletta is seeking a Manager/Sr Manager, Clinical Operations, International. R...
Location
Location
Germany; Switzerland
Salary
Salary:
Not provided
cabalettabio.com Logo
Cabaletta Bio Inc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s Degree or advanced degree in life sciences or related field
  • Minimum 4 years of clinical trial management experience including management of study resources, vendors, budgets, supplies, critical path activities, and risk management, within Biotech or pharmaceutical industry or equivalent by experience
  • Cell therapy experience preferred and/or focus complex therapies
  • Fluency in English
  • working proficiency in additional European languages a plus
  • Experience with early phase, complex trials
  • Experience managing Contract Research Organizations and other external vendors
  • Good understanding of European regulatory requirements (EMA, MHRA, etc)
  • Working knowledge of GCP/ ICH regulatory guidelines
  • Extensive knowledge of standard industry practices related to study start-up, site management and monitoring, document management, and clinical supply management
Job Responsibility
Job Responsibility
  • Provide day-to-day clinical project management oversight of the full range of clinical operations activities associated with clinical trial conduct from protocol development, feasibility/capability assessments, initiation, execution, control, and closure
  • Perform hands-on activities not outsourced to vendors, as needed
  • Author study documents and plans such as ICF and study specific plans
  • Provide input and review of site training materials
  • Review and provide clinical operations input into relevant clinical documents such as the protocol, investigator brochure, regulatory documents, clinical study reports and other documents and plans as appropriate
  • Proactively identify risks and lead team members to mitigate risks in a timely fashion
  • Develop and maintain positive relationships, both internal and external to project, including site personnel (KOLs, PIs, Study Coordinators)
  • Select and manage vendors
  • Perform and document study-level Sponsor Oversight of outsourced clinical activities
  • Execute clinical operations country submission tasks and documents: Review submission pack, coordinate country-specific ethics RFIs, review and update site-specific consent forms
What we offer
What we offer
  • health and retirement
  • PTO
  • stock option plans
Read More
Arrow Right

Clinical Project Manager

Permanent position available immediately located in Paris. The role involves lea...
Location
Location
France , Paris
Salary
Salary:
Not provided
ab-science.com Logo
AB SCIENCE
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Holder of additional training in methodology (CESAM, IUD, …)
  • Successful experience of Clinical Project Manager in a pharmaceutical company or CRO
  • 6-8 year’s experience in clinical development (Phase II and III)
  • Experience in oncology or autoimmune inflammatory diseases would be a plus
  • Experience in international development required
  • Experience of the regulatory environment for clinical trials
  • Experience of writing research reports and FDA regulatory dossiers (IND, NDA) and EMA
  • Fluent in English
Job Responsibility
Job Responsibility
  • Design, implementation and coordination of clinical studies with the support of Clinical Operations, Pharmacovigilance, Biometrics and Medical Writing
  • Plan the clinical development program
  • Prepare studies protocols, amendments and reports
  • Prepare regulatory dossiers
  • Manage relationships with investigators and opinion leaders
What we offer
What we offer
  • Salary and package to define according to skills and experience
  • Fulltime
Read More
Arrow Right

Commercial and Business Development Manager

We are seeking an experienced Commercial and Business Development Manager to lea...
Location
Location
United Kingdom , Oxford
Salary
Salary:
Not provided
welbeckhealthpartners.com Logo
Welbeck Health Partners
Expiration Date
August 31, 2026
Flip Icon
Requirements
Requirements
  • Degree educated or equivalent professional qualification
  • 5+ years’ experience in business development / sales and marketing
  • Proven experience in the business development within the healthcare industry
  • Able to evidence strong knowledge of account management and customer relationship management
  • Demonstrable experience in strategic planning and delivery
  • Experience in commercial delivery, particularly in reporting progress against key metrics and presenting this for senior management
  • Effective presentation and communication skills and comfortable delivering presentations
  • Strong stakeholder management skills and able to balance sometimes conflicting views
  • Proactive individual who can drive forward activities across cross-functional teams and take the lead in often ambiguous circumstances
  • Highly organised and able to coordinate multiple complex projects
Job Responsibility
Job Responsibility
  • Drive growth in centre activity and revenue by formulating and delivering the business development strategy
  • Create, and gain agreement, on the commercial and business development plans linked to revenue generation targets
  • Translate centrally driven commercial strategies into centre focused commercial plans
  • Lead on the design and implementation of centre’s commercial strategy
  • Responsibility for commercial contracts such as local corporates, military bases and health screening contracts
  • Develop and maintain a tactical business development plan
  • Use all marketing and performance data avenues available to monitor, analyse and report activity
  • Leading cross-specialty activities and regularly reviewing progress against plan
  • Build a strong knowledge of our customer base and clinical USPs
  • Maximise patient activity and hospital capacity by supporting efficient scheduling
  • Fulltime
Read More
Arrow Right

Associate Vice President, Clinical Data Management

The Associate Vice President, Clinical Data Management is a member of the Global...
Location
Location
India , Hyderabad
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s or master’s degree with 25+ years of data management experience
  • 10 to 15 years of managerial experience directly managing people and/or leadership experience leading teams, projects, programs or directing the allocation of resources
  • Experience within clinical data management, regulatory compliance, and strategic leadership within a pharmaceutical, biotech, or CRO environment
  • Expertise in GCP, ICH, FDA, EMA regulations, data governance, and clinical trial data standards (CDISC, SDTM)
  • Experience within cross-functional collaborations, leadership, and strategic planning skills, ensuring operational excellence and compliance while driving innovation in data management to support Amgen’s global clinical development efforts
  • Expertise in AI/ML-driven data management solutions, automation, and advanced analytics
  • Understanding of clinical data standards (CDISC, SDTM, ADaM)
  • Experience leading regulatory submissions, including NDA/BLA/MAA filings and advisory committee interactions
  • Proven ability to drive organizational change, optimize processes, and implement lean principles in clinical data management
  • Cross-functional collaboration experience with clinical operations, regulatory affairs, biostatistics, and R&D teams
Job Responsibility
Job Responsibility
  • Develop and drive the global data management strategy in alignment with clinical development objectives and corporate goals
  • Provide strategic and operational leadership to the Clinical Data Management (CDM) function across all clinical programs and phases
  • Lead innovation initiatives, including the implementation of development integration programs and the adoption of cutting-edge technologies to enhance data workflows
  • Represent Clinical Data Management in executive leadership discussions, regulatory interactions, and industry forums
  • Establish and enforce robust clinical data governance models, policies, and risk mitigation strategies to ensure quality and compliance
  • Make final decisions regarding standard operating procedures (SOPs), CDM best practices, and process optimization
  • Engage key stakeholders and ensure timely resolution on critical data integrity and regulatory compliance issues
  • Serve as the primary CDM representative during regulatory inspections and audits, with responsibility for final decisions on findings, responses, and corrective actions
  • Influence cross-functional clinical development, operational, and regulatory strategies through data-driven insights and analytics
  • Partner closely with Clinical Program Operations, Regulatory, Biostatistics, and R&D to ensure seamless integration and alignment of clinical data
Read More
Arrow Right
New

Clinical Trial Manager

Beam is seeking an experienced and motivated Clinical Trial Manager (CTM) to joi...
Location
Location
United States , Cambridge
Salary
Salary:
125000.00 - 155000.00 USD / Year
beamtx.com Logo
Beam Therapeutics
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's Degree in life sciences or related field with 8+ years' experience in biotech and/or pharmaceutical industries managing clinical trials
  • Phase I experience is strongly preferred
  • a background in rare disease and/or metabolic disorders is highly desirable
  • experience with cell & gene therapy is a plus
  • Experience with GCP/ICH Guidelines, and a strong understanding of cross-functional clinical processes
  • Exceptional organizational skills and ability to deal with competing priorities
  • strong reasoning and problem solving ability
  • Ability and willingness to travel up to 20% (domestic and international)
Job Responsibility
Job Responsibility
  • Manage all project team activities related study start up, conduct and close out activities
  • Work with Outsourcing and Contracts Management to ensure Site Contracts reflect trial activities and related budget
  • Manage Change Orders with Sites (and Vendors when necessary)
  • Contribute to development of Informed Consent Form and provide oversight and approval for all country and site level ICF
  • Oversee preparation and submission of essential documents to IRBs/ECs and regulatory authorities
  • Contribute to (or oversee the management of) the creation of the trial plans and site facing documents
  • Develop (or overseeing the development of) all training/day to day materials
  • Support data management activities
  • Monitor (and escalate appropriately) vendor metrics and vendor performance
  • Organize, oversee and/or participate in all study related meetings
  • Fulltime
Read More
Arrow Right
New

Oncology clinical scientist intern

The Global Oncology Internship Program at Johnson & Johnson is a comprehensive l...
Location
Location
Belgium , Beerse
Salary
Salary:
Not provided
https://www.randstad.com Logo
Randstad
Expiration Date
January 25, 2026
Flip Icon
Requirements
Requirements
  • Legally/permanently authorized to work in Belgium with no required sponsorships
  • Must be currently enrolled in an accredited University or College program throughout the duration of the internship
  • Must not be graduating before, during, or after the start or end of the internship program
  • Currently enrolled in biology, cell/molecular biology, chemistry, pre-med, nursing program, public health, biochemistry, biomedical engineering, oncology, clinical pharmacology, clinical or translational research, computational biology, precision medicine, or similar areas of study
  • Undergraduate students with completion of a minimum of four semesters at program start or graduate students are eligible
  • Minimum cumulative GPA of 3.0
  • Students in good standing, working towards the completion of an undergraduate or graduate degrees
  • Graduate students must be pursuing a master’s, PharmD, Physician Assistant or PhD or other clinical related degrees
  • Self-motivated, future scientist leaders passionate about drug development and clinical research
  • Detailed oriented with good organizational skills
Job Responsibility
Job Responsibility
  • Gaining overall understanding of clinical research and drug development including but not limited to Good Clinical Practices (GCPs), International Conference of Harmony (ICH) guidelines, and Standard Operating Procedures (SOPs)
  • Attend “Bench to Bedside” Lecture Series to gain knowledge of the drug development process and clinical research
  • Assisting with management of trial activities including patient tracking through screening process, and eligibility/enrollment reviews
  • Assisting with document processing and management within the electronic master file (i.e., vTMF)
  • Participating in department and team meetings
  • Participating in cross-functional team and clinical team meetings
  • Developing study training materials/documents
  • Shadowing key clinical and or functional roles for learning/development opportunities
  • Observing Site Initiation Visit (SIV) Meetings (if applicable for assigned projects)
  • Supporting Clinical Team with study start up activities during trial set up, and other study tasks during conduct, and close out (depending on the stage of the trial)
What we offer
What we offer
  • We offer an inclusive work culture that is open, innovative, and performance driven
  • Fulltime
Read More
Arrow Right

Technical Project Manager

Premium Health is seeking a highly organized and collaborative Technical Project...
Location
Location
United States , Brooklyn
Salary
Salary:
110000.00 - 130000.00 USD / Year
premiumhealth.org Logo
Premium Health
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s degree in information technology, Computer Science, Healthcare Informatics, or related field
  • 3+ years of experience in IT project management, preferably in a healthcare or nonprofit setting
  • Excellent communication skills, with the ability to translate technical details for non-technical stakeholders
  • Strong organization, time management, and prioritization abilities
  • Critical thinking, problem-solving, and conflict resolution skills
  • Adaptability and comfort managing multiple concurrent projects in a fast-paced environment
  • Strong customer service mindset, with focus on supporting clinical and operational needs
  • Ability to lead cross-functional teams and build consensus across departments
  • Proficiency with project management tools (e.g., MS Project, Wrike, Asana, Jira, Trello)
  • Basic understanding of networking, cloud, security, or database environments
Job Responsibility
Job Responsibility
  • Coordinate the planning and execution of end-to-end project activities for IT initiatives, including scope definition, scheduling, budget tracking, and resource allocation in collaboration with IT leadership
  • Collaborate with internal IT staff, department stakeholders, and external vendors to ensure timely and successful project delivery
  • Translate stakeholders’ needs into clear technical requirements, project plans, and roadmaps
  • Support project budget tracking by gathering cost estimates, tracking expenditures, and coordinating procurement activities, ensuring adherence to purchasing policies
  • Assist with vendor selection, contracting, and procurement processes to support project goals
  • Support project intake and triage by reviewing incoming IT requests, clarifying scope and requirements, and coordinating prioritization with IT leadership and stakeholders
  • Monitor project progress, identify risks, and implement mitigation strategies
  • Review and analyze helpdesk metrics to identify trends, recurring issues, and opportunities for workflow or system improvements, and collaborate with IT leadership to prioritize enhancements
  • Conduct workflow and business process analysis with clinical, administrative, and operational departments to understand current processes and identify opportunities for IT-driven improvements
  • Develop and maintain project documentation, such as charters, timelines, status reports, and post-implementation reviews
What we offer
What we offer
  • Public Service Loan Forgiveness (PSLF)
  • Paid Time Off
  • Medical, Dental and Vision coverage with MERP
  • 403(b) Retirement plan with employer matching contribution
  • Fulltime
Read More
Arrow Right

Senior Technical Project Manager, EHR Integrations

We are seeking an experienced Senior Technical Project Manager to lead interoper...
Location
Location
United States , New York
Salary
Salary:
150000.00 - 200000.00 USD / Year
implicity.com Logo
Implicity
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s or Master’s degree in Computer Science, Engineering, or a related field
  • 5+ years of experience in technical project management, healthcare IT, or EHR integrations
  • Strong understanding of HL7 (V2/V3), FHIR, XML, JSON, and REST APIs
  • Proven experience with integration engines such as Mirth Connect
  • Excellent organizational, communication, and stakeholder management skills
  • Ability to manage multiple complex projects simultaneously in a fast-paced environment
Job Responsibility
Job Responsibility
  • Lead discovery, design, and deployment of EHR integration interfaces for hospital clients
  • Manage project timelines, deliverables, risk mitigation, and stakeholder communication
  • Facilitate functional and workflow discovery sessions with clinical and technical teams
  • Define and validate technical specifications with EHR vendors and internal development teams
  • Contribute to, and maintain interfaces using NextGen Mirth Connect or similar tools
  • Ensure end-to-end data integrity, functional compliance, and alignment with HL7/FHIR standards
  • Conduct testing and troubleshooting to guarantee accurate, reliable data exchange
  • Monitor existing interfaces, resolve data or configuration issues, and escalate as needed
  • Document configurations, best practices, and lessons learned to optimize future deployments
  • Contribute to RFP responses and pre-sales discussions related to EHR integrations
What we offer
What we offer
  • Equity: Stock options (BSPCE equivalent)
  • Health Coverage: Comprehensive medical, dental, and vision insurance (90% company-paid
  • 70% dependents)
  • Retirement: 401(k) with up to 4% company match
  • Time Off: 25 PTO days + 9 paid holidays
  • Parental Leave: 4 weeks fully paid maternity / 2 weeks fully paid paternity leave
  • Remote Flexibility: Fully remote within the U.S.
  • collaboration with global teams (HQ: Paris, France)
  • Regular team events, especially every Thursday evenings
  • Fulltime
Read More
Arrow Right
Welcome to CrawlJobs.com
Your Global Job Discovery Platform
At CrawlJobs.com, we simplify finding your next career opportunity by bringing job listings directly to you from all corners of the web. Using cutting-edge AI and web-crawling technologies, we gather and curate job offers from various sources across the globe, ensuring you have access to the most up-to-date job listings in one place.