Intern - CSL Job at Legends Global (Minneapolis)

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Intern - CSL

We are looking for a self-motivated, enthusiastic individual to join our firm in...

Location

United States , Frisco

Salary:

Not provided

Legends Global

Expiration Date

Until further notice

Requirements

Excellent writing and communication skills with the ability to interact with all levels of the organization and outside contacts in both written and verbal formats
Motivated self-starter with the ability to assimilate new information quickly and work under deadlines
Well-organized with the ability to manage multiple complex tasks simultaneously
Excellent computer skills include proficiency with Microsoft Word, PowerPoint and Excel
Currently enrolled in a university
Minimum grade point average of 3.0

Job Responsibility

Conduct primary industry market research through analysis of past, current and potential future event space users and/or visitors to the market
Assemble and review operational and physical characteristics of existing and planned facilities and destinations
Maintain and expand database of extensive industry trends and characteristics
Summarize results of research and analysis for both internal and external purposes
Develop current and prospective client presentation materials

Parttime

Senior Director, Regional Ecosystem Lead

Serve as CSL's key leader in the key innovation hubs to enhance the CSL external...

Location

United States , San Francisco CA or San Diego CA

Salary:

268000.00 - 328000.00 USD / Year

The Muse

Expiration Date

Until further notice

Requirements

12+ years in biopharma, external innovation, or business development with strong regional network and ecosystem knowledge
Advanced degree required (PhD, MD, or equivalent)
Proven track record of enhancing Pharma senior leadership presence/reputation as a partner of choice in biotech ecosystems to drive BD deal flow
Proven ability to source and evaluate external opportunities and lead deal execution
Strong relationship-building skills with academic, biotech, and investment communities

Job Responsibility

Serve as the key CSL leader within the regional innovation ecosystem, actively sourcing opportunities aligned with all TA strategies and portfolio priorities
Maintain and expand strategic relationships with universities, incubators, accelerators, venture capital firms, and local organizations
Partner closely with TA Search Leads to conduct regional searches, plan engagements and conferences, and share regional insights
Serve as a senior member of deal teams occurring in each region, supporting transactions from identification through due diligence
Organize and represent CSL at local external innovation events
Actively participate as a board member in key industry bodies and associations
Maintain intimate knowledge of internal organizational capabilities, priorities, and SMEs
Provide insights on regional biotech trends, competitive landscape, and innovation hotspots
Work closely with R&D BD, and legal teams to evaluate and integrate external assets

What we offer

Health Insurance
Dental Insurance
Vision Insurance
Life Insurance
Short-Term Disability
Long-Term Disability
FSA
HSA
Mental Health Benefits
Adoption Leave

Fulltime

Clinical System Designer

Clinical System Designer - India. ICON plc is a world-leading healthcare intelli...

Location

India , Bangalore

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

Uses technical, industrial, and interpersonal skills, with some support from project team leads and their people leader, to interpret clinical protocols and customer requirements in order to create clinical data management system (CDMS) designs and non-CDMS component specifications (including electronic Case Report Forms (eCRFs), dynamic eCRF functionality and eCRF edit checks) to meet the needs of the customer and the clinical trial
Responsible for optimal design decisions and the utilization of ICON/client specific standards
Good functional knowledge of at least one clinical data management system and CRF design tool
Ability to plan and design CDMS components directly from interpretation of low to medium complexity clinical trial protocols
Acts as first point of contact during study build for assigned projects for design related questions by the project team
Read, ensure understanding and adhere to the study protocol, contract and scope of work for all task during set-up, maintenance and close-out of the study
Tracks and keeps functional management and those responsible for project management informed of any issues that might affect project target dates, scope or budget and escalates potential problems effectively and in a timely manner
With support, consolidates and completes the high-level system requirements documents and facilitates their review
Assumes responsibility for copying and modifying CRFs from standard libraries and other studies
Assumes responsibility for development of Custom CRF screens, Edit Check and Dynamic Check specification documents, using prototyping methodologies as needed

Job Responsibility

Uses technical, industrial, and interpersonal skills, with some support from project team leads and their people leader, to interpret clinical protocols and customer requirements in order to create clinical data management system (CDMS) designs and non-CDMS component specifications (including electronic Case Report Forms (eCRFs), dynamic eCRF functionality and eCRF edit checks) to meet the needs of the customer and the clinical trial
Responsible for optimal design decisions and the utilization of ICON/client specific standards
Good functional knowledge of at least one clinical data management system and CRF design tool
Ability to plan and design CDMS components directly from interpretation of low to medium complexity clinical trial protocols
Acts as first point of contact during study build for assigned projects for design related questions by the project team
Read, ensure understanding and adhere to the study protocol, contract and scope of work for all task during set-up, maintenance and close-out of the study
Tracks and keeps functional management and those responsible for project management informed of any issues that might affect project target dates, scope or budget and escalates potential problems effectively and in a timely manner
With support, consolidates and completes the high-level system requirements documents and facilitates their review
Assumes responsibility for copying and modifying CRFs from standard libraries and other studies
Assumes responsibility for development of Custom CRF screens, Edit Check and Dynamic Check specification documents, using prototyping methodologies as needed

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.

Fulltime

Lead Clinical Site Ambassador

The Lead Clinical Site Ambassador is accountable for the strategic and operation...

Location

United States

Salary:

131000.00 - 164000.00 USD / Year

The Muse

Expiration Date

Until further notice

Requirements

At minimum, bachelor's degree or equivalent in life science, nursing, pharmacy, medical laboratory technology, or other health/medical related area preferred
A minimum of 10 years' relevant clinical research (or related) experience within the pharmaceutical industry
Previous experience in leading and managing a team of professional staff
A solid understanding of the drug development process, and specifically, each step within the clinical trial process
Experience in site management and monitoring and overseeing large and/or complex global clinical trials
Robust budget forecasting and management experience
Thorough knowledge of ICH guidelines/GCP and its applicability to all stages of the clinical development process

Job Responsibility

Responsible for operational oversight of the site, site health and monitoring activities
Support QA audit and inspection planning, and implementation of CAPAs as needed
Identify and proactively mitigate site-level risks impacting recruitment, retention, data quality, or compliance, in partnership with CROs
Provide study support on escalated site issues related to study delivery by coordinating communications and resolution efforts
Support sites in understanding study expectations, timelines, and required deliverables
Be accountable for effective site recruitment planning and delivery, consistent with global and/or country plan and local targets in collaboration with CROs
Responsible for enrollment support and ensure progress by responding to recruitment issues from investigators/CROs
Build and maintain strong, trusted relationships with investigators and site staff - Face of CSL
Serve as the sponsor primary point of contacted for assigned studies
Understand site capabilities, constraints, and strategic priorities to improve site engagement and long-term collaboration

What we offer

Health Insurance
Dental Insurance
Vision Insurance
Life Insurance
Short-Term Disability
Long-Term Disability
FSA
HSA
Mental Health Benefits
Adoption Leave

Fulltime

Field Medical Advisor Cardiorenal

The Field Medical Advisor - Cardiorenal builds and maintains strong scientific r...

Location

Netherlands

Salary:

Not provided

The Muse

Expiration Date

Until further notice

Requirements

University degree in Medicine, Pharmacy, or a Master of Science in Biomedical Sciences
Minimum of 3 years' experience in the pharmaceutical or biotechnology industry (medical, clinical, or specialty products)
Strong ability to apply and leverage scientific and medical knowledge
Excellent negotiation, influencing, and leadership skills
Strong presentation, interpersonal, and communication skills
Proven ability to establish and manage relationships with external experts
Demonstrated business planning, organizational, and project management skills
Innovative and strategic thinking capabilities
Solid understanding of pharmaceutical industry regulations governing medical information and customer interactions, with strong medical governance expertise
Ability to work independently, proactively, and with a high level of self-motivation

Job Responsibility

Build and maintain trusted scientific relationships with External Experts (EEs), HCPs, and key stakeholders within the medical and scientific community
Act as a high-quality scientific liaison between CSL and external medical experts
Respond to unsolicited local medical and scientific inquiries in a timely, accurate, and customer-focused manner
Lead and actively contribute to Scientific Advisory Board meetings
Actively participate in scientific congresses, medical meetings, and symposia, including support for CSL-sponsored programs
Facilitate the review and development of collaborative and investigator-initiated research proposals
Support and conduct site feasibility assessments
Develop, implement, and actively manage engagement and development plans for identified External Experts
Facilitate speaker development and participation at local, regional, and international levels
Support appropriate External Expert development through involvement in clinical trials

What we offer

Health Insurance
Dental Insurance
Vision Insurance
Life Insurance
Short-Term Disability
Long-Term Disability
FSA
HSA
Mental Health Benefits
Adoption Leave

Fulltime

Procurement Specialist

Join a talented team of engineering professionals at Vogt Power International In...

Location

United States , Louisville

Salary:

70000.00 - 90000.00 USD / Year

Babcock Power

Expiration Date

Until further notice

Requirements

A Bachelor's of Science degree in engineering or bachelors of science in business from an accredited university
In lieu of a college degree, applied experience within the fields of construction, subcontract management or purchasing may be substituted at the discretion of VPI management
A knowledge of general steel fabrication management practices applicable to VPI products at a level typically possessed by an individual with 5 years of experience
Good verbal and written communication skills to clearly communicate subcontracting and manufacturing issues to supplies and within VPI
Experience in managing subcontracts or other procurement related activities
Be well-organized, results oriented, and competent sourcing professional, with the highest integrity and work ethic, with time management skills to adapt to unexpected changes, customer emergencies, and priority changes
Must have valid passport for international travel

Job Responsibility

Responsible for managing agreements with subcontractors
Communication of VPI initiated changes in scope to subcontractors and resolution of any changes on price, delivery, or technical capability with the subcontractor
Communicate and resolve changes on pricing, delivery, or subcontractor capabilities with the Project Manager
Responsible for managing the sourcing plan and for monitoring subcontractor performance
Responsible for development of RFQ’s for subcontracted work and for the evaluation of subcontractor quotations
Ensure any selected supplier is an approved / qualified source for commodity listed in the Corporate Supplier List (CSL)
Ensure all commercial documents have been conformed / revised to final agreed set of terms and conditions prior to issue of any Purchase order
Create, and submit a Bid Evaluation through the Deviation Management System (DMS) system
Review Document Control Automation Program (DCAP) packages to confirm all documents are accurate
Responsible for communication of information to subcontractors such as drawings, schedules, and shipping information

Vaccine Sales Specialist

You will be a customer-facing Vaccine Sales Specialist promoting main brands to ...

Location

United States , Hartford

Salary:

Not provided

The Muse

Expiration Date

Until further notice

Requirements

Bachelor's Degree required, preferred in Business, Communication, Health Policy, Life Sciences, Healthcare
1-2 or more years of Pharmaceutical or B2B sales / or relevant healthcare/clinical educational experience
Experience establishing communication and engagement with customers with emphasis on scientific knowledge
Some overnight and meeting travel required

Job Responsibility

Build a multi-specialty group of important accounts within several customer segments
Contact potential customers and negotiate product formulary acceptance
Obtain contract commitments for CSL Seqirus products
Deliver flu portfolio product sales in important accounts including Pediatrics, IDN, FQHCs, and independent/corporate owned HCPs
Develop appropriate value-added programs for each account by understanding customer needs and aligning brand resources to achieve defined goals while demonstrating CSL Seqirus values
Work directly with Regional Sales Manager and Account Managers to prioritize important accounts and lead strategic goals set forth by the commercial organization
Contract and create opportunity for sales growth in designated segments
Conduct routine collaborative meetings with your team to implement tactical plans set forth by sales and marketing
Cultivate a close relationship with colleagues in Sales, Medical Affairs, Marketing, and Customer Service departments to support field efforts to grow the business
Conduct some overnight travel

What we offer

Medical
Dental
Vision
Life Insurance
401K
PTO available from your first day of hire
Health Insurance
Dental Insurance
Vision Insurance
Life Insurance

Fulltime

Vaccine Sales Specialist

You will be a customer-facing Vaccine Sales Specialist promoting main brands to ...

Location

United States , Albany

Salary:

85000.00 - 95000.00 USD / Year

The Muse

Expiration Date

Until further notice

Requirements

Bachelor's Degree required, preferred in Business, Communication, Health Policy, Life Sciences, Healthcare
1-2 or more years of Pharmaceutical or B2B sales / or relevant healthcare/clinical educational experience
Experience establishing communication and engagement with customers with emphasis on scientific knowledge
Some overnight and meeting travel required

Job Responsibility

Build a multi-specialty group of important accounts within several customer segments
Contact potential customers and negotiate product formulary acceptance
Obtain contract commitments for CSL Seqirus products
Deliver flu portfolio product sales in important accounts including Pediatrics, IDN, FQHCs, and independent/corporate owned HCPs
Develop appropriate value-added programs for each account by understanding customer needs and aligning brand resources to achieve defined goals while demonstrating CSL Seqirus values
Work directly with Regional Sales Manager and Account Managers to prioritize important accounts and lead strategic goals set forth by the commercial organization
Contract and create opportunity for sales growth in designated segments
Conduct routine collaborative meetings with your team to implement tactical plans set forth by sales and marketing
Cultivate a close relationship with colleagues in Sales, Medical Affairs, Marketing, and Customer Service departments to support field efforts to grow the business
Conduct some overnight travel

What we offer

Medical
Dental
Vision
Life Insurance
401K
PTO available from your first day of hire
Health Insurance
Dental Insurance
Vision Insurance
Life Insurance

Fulltime

Intern - CSL

Legends Global

Location:
United States , Minneapolis

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
February 20, 2026

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Intern - CSL

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Location:United States , Minneapolis

Category:Research and Development

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Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:February 20, 2026

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

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Intern - CSL

Senior Director, Regional Ecosystem Lead

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Vaccine Sales Specialist

Vaccine Sales Specialist

Location:
United States , Minneapolis

Category:
Research and Development

Contract Type:
Not provided

Job Posted:
February 20, 2026