CrawlJobs Logo

Intern, Clinical Pharmacology

biomarin.com Logo

BioMarin Pharmaceutical

Location Icon

Location:
United States , San Rafael

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. The Clinical Pharmacology group is responsible for the design, execution, interpretation, and reporting of nonclinical and clinical pharmacology aspects of BioMarin’s development and commercial pipeline. This includes the assessment of PK/PD relationships of small molecule, biologic and gene therapy drug candidates that are situated throughout all stages of development(Phase 0-IV). Team members are responsible for the planning, implementation, and organization of regulatory filings along with presentation of clinical pharmacology data to internal cross-functional teams, external collaborators, US and ex-US regulatory authorities and the scientific community. The assignment will span a period of 10-12 weeks.

Job Responsibility:

  • Design, analysis, interpretation, and reporting of PK/PD studies in support of molecules in nonclinical and clinical development
  • Work with Clinical Pharmacology leaders on projects and provide support in designing the Clinical Pharmacology strategy with an emphasis on dose and regimen selection
  • Core clinical pharmacology activities with specific tasks targeted to answer key development questions and achieve short-term goals for the department
  • Internal presentation of results of project to leadership & publish the findings at a scientific conference

Requirements:

  • Strong training in PK/PD analyses with a preference for population-based modeling and simulation
  • Extensive hands-on experience with non-compartmental and compartmental PK/PD analysis software
  • Excellent writing and verbal communication skills
  • Graduate level student with a strong interest in Clinical Pharmacology, Pharmacokinetics, PK/PD Modeling and Simulation
  • Student must be returning to school in the Fall Term OR has graduated within the 1 year of the start of the program
  • Must be available to work 40 hours a week
  • Must be authorized to work in the United States without visa sponsorship

Nice to have:

  • Experience in clinical/nonclinical PK/PD study design, implementation, and interpretation
  • Ability to work in a matrix environment and with different leadership styles
What we offer:
  • Paid hourly wage
  • Paid company holidays
  • 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:
On-site 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, Clinical Pharmacology

New

Clinical Study Team Assistant

As a part of the global Project Leadership group at Parexel, you are responsible...
Location
Location
Salary
Salary:
Not provided
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s Degree (B.S. or B.A.) in either a Scientific or Business-related field preferred or equivalent relevant experience
  • Minimum 2 - 3 years experience in clinical administration in pharmaceutical or clinical research environment
  • Solid experience in TMF
  • Experience in WORD, EXCEL, PowerPoint, other software and system
  • Fundamental understanding of filing systems and organizational tools
  • Proficiency in written and spoken English
  • Able to independently prioritize multiple key activities, collaborate effectively with various levels of seniority on the study team and across the organization and efficiently ensure completion of tasks per timelines to required quality standards
  • Able to work independently and proactively to anticipate team needs related to clinical trial services
  • Demonstrated effectiveness working with multiple functions in a professional manner
  • Effective verbal and written communication skills relating to colleagues and associates both inside and outside the organization
Job Responsibility
Job Responsibility
  • Provide Client Trial Master File (TMF) support and maintenance – file & ensure documents are in the TMF
  • Input into the set- up of TMF document list and maintains relevant clinical trial documents according to International Conference on Harmonization-Good Clinical Practices (ICH-GCP) and Standard Operation Procedures (SOPs), including archiving and electronic filing of documents (TMF)
  • Accountable for analyzing, interpreting and evaluating clinical trial documentation to determine appropriateness for inclusion into the TMF
  • Evaluate TMF compliance and raise findings to Study Manager (SM)
  • Files and tracks documents for the study in collaboration with the document owner
  • Collaborates with the TMF Study Owner for issues or problems to be addressed and to create and manage placeholders
  • Ensures resolution of Quality Control (QC) findings (as delegated) to support final archive of the clinical study documents
  • Maintain, verify, process, and makes updates to Client systems (including Registry), spreadsheets/documents as needed
  • For Early Development and some small/single country studies may be required to: Coordinate Clinical Study Agreement approvals to ensure timely site initiation
  • Responsible for coordinating the clinical trial application to ethics committee and regulatory authority
What we offer
What we offer
  • Supportive work environment
  • High degree of empowerment and accountability
  • Work with a diverse set of clients and therapeutic areas
  • Encouraged to take on new challenges and pursue your interests
  • Supportive and inclusive environment
  • Flexible work arrangements
  • Remote, in-office and hybrid roles
  • Varied project experience
  • Career progression
  • Fulltime
Read More
Arrow Right

Medical Director/Senior Medical Director, Clinical Development, Genetic Diseases

The Medical Director in Clinical Development will serve as the Medical Lead for ...
Location
Location
United States , Cambridge
Salary
Salary:
210000.00 - 375000.00 USD / Year
beamtx.com Logo
Beam Therapeutics
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • MD, DO or equivalent ex-US medical degree with 15+ years experience
  • Minimum of 4 years of Pharmaceutical/Biotech industry experience in clinical development and medical monitoring
  • Board certification/eligibility in endocrinology or metabolic disorders, or another relevant specialty highly desired
  • Strong oral and written communication skills to influence others
  • Ability to work collaboratively in a fast-paced, team-based matrix environment and to function independently as appropriate
  • Clinical development and/or clinical experience in rare disease, cell & gene therapy is a plus
  • Ability to work independently to resolve challenges
Job Responsibility
Job Responsibility
  • Serves as the Clinical Development lead on the cross-functional Program Team and co-lead the Clinical Development Sub-team for assigned programs
  • Support development of Target Product Profile (TPP) and Clinical Development Plan (CDP)
  • Serves as the medical monitor for assigned studies including design, execution and interpretation study data
  • Provides scientific and clinical input to study-related documents and analysis plans including Informed consent forms (ICF), clinical research forms (CRF), statistical analysis plans (SAP), clinical pharmacology and biomarker analysis plans
  • Ensure patient safety on clinical trials and adherence to Good Clinical Practices (GCP)
  • Contribute to the development of regulatory documents in support of regulatory submissions, including clinical section of IND's and CTA's, safety reports, responses to regulatory authorities and Ethics Committees/IRBs, and other documents as appropriate
  • Acts as liaison between Clinical Development and other internal groups at BEAM for assigned studies
  • Establishes strong collaborations with study investigators, outside medical experts and represents BEAM during investigator meetings and advisory boards
  • Contribute to the development and planning of Advisory Board meetings in the relevant therapeutic areas
  • Fulltime
Read More
Arrow Right

Director/Senior Director of Clinical Research

Join Hemab, a clinical-stage biotech company, on an exciting journey to build th...
Location
Location
Denmark , København
Salary
Salary:
Not provided
life-science-talent-solutions.dk Logo
Life Science Talent
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Advanced degree (MD, PhD, PharmD) in life science or health science field
  • 5+ years in clinical development within biotech/pharmaceutical industry or equivalent professional experience
  • Proven track record executing Phase I-III clinical trials
  • Strong understanding of regulatory environment and experience with regulatory interactions
  • Extensive knowledge of GCP, clinical trial methodology, clinical processes, and regulatory requirements
  • Demonstrated leadership with strong strategic and analytical thinking abilities
  • Excellent communication and presentation skills
  • Collaborative approach with ability to work across functions
  • Strong organizational skills and ability to manage multiple priorities
  • Comfortable in fast-paced biotech environment
Job Responsibility
Job Responsibility
  • Develop clinical development strategies, study designs, and protocols that meet scientific and regulatory objectives
  • Oversee clinical trial documentation and study execution, including endpoint selection, medical monitoring, and clinical trial data review/interpretation
  • Monitor program progress and develop contingency plans as needed
  • In collaboration with Clinical Operations, responsible for oversight of study enrolment and timelines for key deliverables
  • Collaborate with Discovery teams to identify and interrogate new drug candidates
  • Support regulatory submissions and documentation
  • Ensure adherence to GCP, ICH guidelines, and company policies
  • Work closely with Clinical Operations, Clinical Science, Biostatistics, Regulatory Affairs, Medical Affairs, Quantitative Clinical Pharmacology and Safety/Pharmacovigilance teams to generate and deliver high-quality clinical data to support scientific and corporate objectives
  • Partner with key opinion leaders and subject matter experts to support study design and strategic elements of the CDP
  • Manage relationships with clinical study sites/investigators, CROs, vendors, and consultants
  • Fulltime
Read More
Arrow Right

Senior Medical Marketing Manager

As the company's medical science expert for designated therapeutic areas, establ...
Location
Location
China , Beijing
Salary
Salary:
Not provided
coloplast.com Logo
Coloplast
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Master's or doctoral degree in clinical medicine, pharmacy, pharmacology, or related life sciences (MD, PhD, PharmD preferred)
  • At least 5 years Medical advisor experience in MNC pharmaceutical or medical device companies
  • Deep understanding of medical and clinical benefits of strategic products with business acumen
  • Strong process and numerical skills with an analytical approach to marketing and ability to identify and report on trends and insights
  • Highly self-motivated and willing to win attitude
  • Multi tasks & priority setting skill
  • Logic thinker & good analytic skill
  • Good English skill (including writing, reading and oral)
  • Team spirit
  • Good presentation skills (Including being well versed in MS Office applications)
Job Responsibility
Job Responsibility
  • Annual medical marketing and medical education plan development which is aligned with ABP & medical marketing strategies and plan
  • Provide medical and scientific input to promote a higher standard of ostomy care, thereby strengthening Coloplast leading position today and in the future
  • Plan post-market clinical studies to address evidence gaps and support product differentiation advantages. Conduct in-depth medical interpretation of existing clinical data to generate medical insights
  • Develop strong partnerships with national KOLs and gather KOL insights to drive stronger strategic medical perception and product adoption and usage with cutting edge medical evidence and educational material/tools
  • Organize and participate in AB meetings to conduct in-depth discussions on academic promotion strategies
  • Respond promptly, accurately, and in compliance to complex medical inquiries raised by external experts and internal colleagues
  • Responsible for developing and managing medical information materials, including medical reference manuals, product evidence summaries, and compilations of the latest clinical data
  • Conduct medical review of all external materials (including PPTs, DA, meeting materials, etc.) to ensure scientific accuracy, balanced content, and compliance with regulations and company policies
  • Provide in-depth content and training support to the sales, marketing and market access teams on topics such as disease knowledge, product functions, clinical data and information on competing products
  • Provide comprehensive medical support and preparatory work for new product launches and approvals of new indications
Read More
Arrow Right

Senior Medical Marketing Manager

As the company's medical science expert for designated therapeutic areas, establ...
Location
Location
China , Beijing
Salary
Salary:
Not provided
coloplast.com Logo
Coloplast
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Master's or doctoral degree in clinical medicine, pharmacy, pharmacology, or related life sciences (MD, PhD, PharmD preferred)
  • At least 5 years Medical advisor experience in MNC pharmaceutical or medical device companies
  • Deep understanding of medical and clinical benefits of strategic products with business acumen
  • Strong process and numerical skills with an analytical approach to marketing and ability to identify and report on trends and insights
  • Highly self-motivated and willing to win attitude
  • Multi tasks & priority setting skill
  • Logic thinker & good analytic skill
  • Good English skill (including writing, reading and oral)
  • Team spirit
  • Good presentation skills (Including being well versed in MS Office applications)
Job Responsibility
Job Responsibility
  • Annual medical marketing and medical education plan development which is aligned with ABP & medical marketing strategies and plan
  • Provide medical and scientific input to promote a higher standard of ostomy care, thereby strengthening Coloplast leading position today and in the future
  • Plan post-market clinical studies to address evidence gaps and support product differentiation advantages. Conduct in-depth medical interpretation of existing clinical data to generate medical insights
  • Develop strong partnerships with national KOLs and gather KOL insights to drive stronger strategic medical perception and product adoption and usage with cutting edge medical evidence and educational material/tools
  • Organize and participate in AB meetings to conduct in-depth discussions on academic promotion strategies
  • Respond promptly, accurately, and in compliance to complex medical inquiries raised by external experts and internal colleagues
  • Responsible for developing and managing medical information materials, including medical reference manuals, product evidence summaries, and compilations of the latest clinical data
  • Conduct medical review of all external materials (including PPTs, DA, meeting materials, etc.) to ensure scientific accuracy, balanced content, and compliance with regulations and company policies
  • Provide in-depth content and training support to the sales, marketing and market access teams on topics such as disease knowledge, product functions, clinical data and information on competing products
  • Provide comprehensive medical support and preparatory work for new product launches and approvals of new indications
Read More
Arrow Right

Senior Medical Writer

The Senior Medical Writer: 1) writes original content for publications activitie...
Location
Location
United States , West Chester
Salary
Salary:
Not provided
synchronygroup.com Logo
Synchrony Group
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • PhD, PharmD, or MD
  • Minimum of 3 years’ experience in medical communications
  • Substantial professional medical writing experience in a wide variety of communication formats
  • Ability to work independently on assigned projects
  • Excellent attention to detail and high degree of scientific and medical accuracy
  • Ability to manage outcomes to win-win resolution
  • Ability to identify key issues and to creatively and strategically overcome challenges or obstacles
  • High level of integrity, ethics, confidentiality, and accountability
  • Sound analytical thinking, planning, prioritization, and execution skills with an ability to multitask
  • Well-developed professional communication skills, including written and interpersonal
Job Responsibility
Job Responsibility
  • Demonstrate a command of assigned therapeutic areas and expertise with assigned products
  • Write original content for publication/communication activities (primary and review manuscripts, abstracts, posters), slide presentations, meeting summaries, and other materials for HCP and internal audiences
  • Prepare materials according to internal writing guidelines and other applicable guidelines (eg, client-specific style guidelines, compliance best practices, journal style guidelines)
  • Follow all internal processes and procedures with regard to workflow, development of deliverables, and adherence to industry best practices, including GPP3
  • Demonstrate the flexibility/adaptability necessary to function on different therapeutic teams as needed
  • Interpret and apply clinical data
  • Maintain a proactive approach on initiatives for existing and prospective clients
  • Work in conjunction with team members to manage workload and develop and adhere to logical and attainable timelines for project completion
  • Attend team meetings to provide input and aid in troubleshooting/problem-solving
  • Efficiently and accurately collate and incorporate author/client comments
What we offer
What we offer
  • Competitive salaries
  • Generous paid time off
  • Excellent health insurance
  • Family leave
  • 401(k) plan with employer matching
  • Fulltime
Read More
Arrow Right

Licensing Business Development Manager

Mantell Associates is partnered with a rapidly scaling preclinical CRO empowerin...
Location
Location
United States , San Francisco
Salary
Salary:
Not provided
mantellassociates.com Logo
Mantell Associates
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Advanced scientific degree (Ph.D. preferred) in biomedical sciences, immunology, pharmacology, cancer biology, or related fields
  • Strong foundational experience in antibody development or biologics discovery and a solid understanding of life science R&D and licensing processes
  • Demonstrated experience in business development, licensing or strategic partnerships within biotech, pharma or related sectors
  • Exceptional strategic thinking, analytical capabilities and commercial judgement
  • Excellent communication, presentation, negotiation and interpersonal skills across diverse stakeholders
  • Ability to manage complex, matrix-driven projects in a fast-paced environment
Job Responsibility
Job Responsibility
  • Identify and cultivate external business opportunities for licensing, co-development and other structured transactions with biotech and pharma organisations
  • Lead the preparation and presentation of robust business cases for prioritized opportunities with clear strategic insights, assumptions and risk assessments
  • Manage end-to-end opportunity progression including due diligence, proposal development, negotiations, deal structuring and closure
  • Coordinate cross-functional diligence and alliance management with internal teams (R&D, clinical sciences, regulatory affairs, operations, finance) and act as a primary BD contact where required
  • Contribute to the refinement of business development and licensing strategies aligned with corporate goals
  • Represent the company at industry partnering events and networking forums to build and sustain stakeholder relationships
  • Fulltime
Read More
Arrow Right

Licensing Business Development Manager

Mantell Associates is partnered with a rapidly scaling preclinical CRO empowerin...
Location
Location
United States , San Diego
Salary
Salary:
Not provided
mantellassociates.com Logo
Mantell Associates
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Advanced scientific degree (Ph.D. preferred) in biomedical sciences, immunology, pharmacology, cancer biology, or related fields
  • Strong foundational experience in antibody development or biologics discovery and a solid understanding of life science R&D and licensing processes
  • Demonstrated experience in business development, licensing or strategic partnerships within biotech, pharma or related sectors
  • Exceptional strategic thinking, analytical capabilities and commercial judgement
  • Excellent communication, presentation, negotiation and interpersonal skills across diverse stakeholders
  • Ability to manage complex, matrix-driven projects in a fast-paced environment
Job Responsibility
Job Responsibility
  • Identify and cultivate external business opportunities for licensing, co-development and other structured transactions with biotech and pharma organisations
  • Lead the preparation and presentation of robust business cases for prioritized opportunities with clear strategic insights, assumptions and risk assessments
  • Manage end-to-end opportunity progression including due diligence, proposal development, negotiations, deal structuring and closure
  • Coordinate cross-functional diligence and alliance management with internal teams (R&D, clinical sciences, regulatory affairs, operations, finance) and act as a primary BD contact where required
  • Contribute to the refinement of business development and licensing strategies aligned with corporate goals
  • Represent the company at industry partnering events and networking forums to build and sustain stakeholder relationships
  • Fulltime
Read More
Arrow Right