Licensed Practical Nurse/Registered Practical Nurse Jobs

New

Licensed Practical Nurse/Registered Practical Nurse

Bayshore is looking for caring and knowledgeable Licensed Practical Nurses/Regis...

Location

Canada , Northern Quebec - Remote regions

Salary:

Not provided

Bayshore HealthCare

Expiration Date

Until further notice

Requirements

A diploma from a recognized school and valid license with the OIIAQ, in order to practice according to provincial regulations
6 months of full-time experience as an LPN/RPN (also called auxiliary nurse or Nursing Assistant)
CPR training an asset. (may be completed at time of hire / prior to first assignment)
Excellent command of spoken and written French
Fluency in English an asset
Has a reliable means of transport (bus, train, etc.) OR a valid driver’s license and a reliable vehicle for travel
No criminal record and be able to obtain a vulnerable sector check, if applicable
Must be fully vaccinated against COVID-19 as directed by Health Canada (e.g., two doses of a two-dose vaccine series or one dose of a single-dose vaccine series)

Job Responsibility

Actively participate in the observation and collection of data on the condition of patients
Ensure follow-up with the multidisciplinary team
Provide direct patient care
Demonstrate excellent active listening skills as well as empathy towards the patients and their families

What we offer

Competitive salary
Comprehensive benefits for you and your family
Wide variety of work options
Continuous learning
Access to healthcare experts
Control of your schedules and destinations
Option to apply for assignments that interest you
No minimum hours
Adapt your schedules to your lifestyle
Opportunity to work in various healthcare establishments of Quebec

New

Senior Customer Success - Enterprise Account Manager

Join Beamy, a fast-growing SaaS company, as a Senior Customer Success - Enterpri...

Location

France , Paris

Salary:

90000.00 - 110000.00 EUR / Year

Beamy

Expiration Date

Until further notice

Requirements

At least 8 years of experience within B2LargeB ensuring customer satisfaction & business sustainability
Experience working with large companies on organisational and process issues
Ability to adopt a consultative stance to understand client's challenges and suggest solutions
Know how to develop and implement renewal and upsell strategies
Fluent in French
Very good level in Business English

Job Responsibility

Ensure the ROI by working closely with key accounts to define clear business objectives, timelines, priorities, and metrics of success
Be the trusted advisor in SaaS Governance by organizing and leading a community of customers
Be the main contact of the partnership by ensuring robust sponsorship across diverse stakeholders
Coordinate the customer journey at Beamy and set the tempo by delegating
Ensure Contract Renew & Upsell

What we offer

Stock options
Hybrid remote work (3 days per week at the office)
Culture of Transparency
Clear paths for career progression
Health insurance (Alan)
Meal vouchers (Swile)
5 weeks of vacation plus additional time off (RTT)

Fulltime

New

Medical Science Liaison

This Director (or Associate Director) level MSL will own a defined US territory ...

Location

United States , Chicago/Minneapolis

Salary:

180000.00 - 220000.00 USD / Year

Beam Therapeutics

Expiration Date

Until further notice

Requirements

Advanced scientific degree (PharmD, PhD, MD, or equivalent)
~10+ years industry experience in Medical Affairs with significant Field Medical tenure
Rare disease expertise required
hematology strongly preferred with emphasis on SCD
Small biotech experience preferred
demonstrated impact in resource‑constrained settings
Launch experience (pre‑approval to post‑launch), ideally in CGT or complex specialty (buy‑and‑bill) environments
Proven territory management and account planning capability across complex ecosystems (academic centers, community networks, payers, advocacy)
Independent, proactive operator with strong ownership
Cross‑functional collaboration with Clinical, Regulatory, Commercial, Medical Operations, and Publications while maintaining medical/scientific integrity

Job Responsibility

Develop and execute territory strategy: map treatment centers, referral networks, transplant/infusion sites, cell-collection capabilities, payers, and advocacy groups
prioritize accounts and set measurable objectives
Support treatment center onboarding: coordinate scientific and operational readiness aligned with SOPs, compliance, and patient journey requirements
partner with internal teams for qualification and activation
Build trusted relationships with KOLs and HCPs: deliver fair-balanced, evidence-based education on rare diseases, cell and gene therapy science, and Beam’s platform
foster advocacy and awareness
Educate stakeholders on disease state, therapeutic landscape, and company platform to drive awareness and credibility in the rare disease and CGT space
Generate high-quality insights from field interactions: synthesize trends and communicate actionable recommendations to Medical Affairs leadership and cross-functional partners
Collaborate on pre-launch planning: align with Medical Strategy, Publications, Medical Information, Value & Evidence, and Medical Operations to ensure scientific messaging, data dissemination, and field tools are ready for first commercial launch
Support clinical research activities: identify potential sites, assist with feasibility assessments, and promote best practices for enrollment and retention while maintaining medical/scientific independence

Fulltime

New

Associate Director/Director, Patient Advocacy & Centricity

Beam is looking for a highly energetic and motivated Associate Director/Director...

Location

United States , Cambridge

Salary:

180000.00 - 260000.00 USD / Year

Beam Therapeutics

Expiration Date

Until further notice

Requirements

8+ years of biopharmaceutical/industry experience with 4+ years of patient advocacy experience
Bachelor’s degree required / Advanced degree such as MS, RN, LCSW, CGC preferred
Effective communicator (verbal and written) and strong interpersonal skills that can build and progress relationships internally and externally
Ability to lead and independently drive projects forward with tangible results
Must be agile and able to adapt to the quick pace of a rapidly growing company
Travel: 25-35% (patient meetings, headquarters.)

Job Responsibility

Engage and partner with patient advocacy organizations, key opinion leaders, policy makers, and patients/caregivers to advance Beam’s patient-oriented objectives and mission
Identify and advance projects, programs, and events to understand and address patient and caregiver needs in the rare disease communities
Collaborate with clinical development and regulatory functions to include the patient perspective in clinical trial design
Compliantly educate advocacy groups and patients on Beam clinical development programs
Collaborate with professional organizations and key opinion leaders to support advocacy and policy engagement and educate on Beam’s science, research, and development programs
Build and lead relationships with various advocacy groups and professional organizations to ensure productive partnerships and alliance
Implement strategies to drive disease awareness, patient speaker engagement, clinical trial awareness, and policy improvements
Oversee company-sponsored patient advocacy events to appropriately engage employees and champion the patient voice and experience to further the patient-centric mindset
Interfaces with medical affairs when a part of the organization to ensure coordination and alignment with KOL, ad boards and medical education activities
Serves as a representative of the organization to ensure information communicated is accurate and up to date regarding organizational activities and industry trends

Fulltime

New

Engineer / Sr Engineer, Manufacturing Sciences & Technology (mRNA/LNP)

Beam is looking for a highly motivated Engineer/Senior Engineer to join our grow...

Location

United States , Cambridge, MA

Salary:

100000.00 - 135000.00 USD / Year

Beam Therapeutics

Expiration Date

Until further notice

Requirements

Ph.D. in Chemical Engineering, Bioengineering, Biochemistry, or equivalent with minimum 6 years of relevant work experience
M.S. degree with a minimum of 8 years of relevant work experience
B.S. degree with a minimum 10 years of relevant work experience
Demonstrated experience in technology transfer, scale-up, and implementation of downstream unit operations, such as tangential flow filtration, normal flow filtration, and chromatography
Experience in executing Process Validation lifecycle approach
i.e. process design, PPQ, and CPV
Experience in leading cross-functional teams for non-conformance event investigations, Root Cause Analyses (RCAs), and CAPAs
Outstanding written, verbal, and presentation skills
ability to communicate strategies, plans, and results to a diverse audience
Ability to simultaneously manage multiple projects and priorities and adjust quickly to dynamic situations

Job Responsibility

Supports MS&T activities related to mRNA and LNP programs
Supports the technology transfer and implementation of mRNA and LNP GMP manufacturing processes, collaborates with sending and receiving site cross-functional team members
Supports bulk drug substance and bulk drug product manufacturing across the full product lifecycle, including process design, process performance qualification (PPQ), commercial production, and continued process verification (CPV)
Authors technical documentation, including technology transfer plans, facility fit and gap analysis reports, manufacturing study protocols and reports, and risk assessments
Supports equipment design to meet process needs and compliance/regulatory expectations
supports Engineering and Validation departments with subsequent procurement, qualification, and GMP readiness
Supports regulatory submissions, responses, on-site audits, and inspections
Represents MS&T in cross-functional teams related to mRNA/LNP programs and manufacturing operations
Provides person-in-plant (PIP) support in manufacturing at Beam Durham
Supports MS&T lab and non-GMP analytical testing of in-process intermediates, as needed

Fulltime

New

Manager/Sr. Manager, Global Compliance and Training

The Manager/Sr. Manager, Compliance and Training, will provide expertise in trai...

Location

United States , Durham, NC

Salary:

125000.00 - 190000.00 USD / Year

Beam Therapeutics

Expiration Date

Until further notice

Requirements

University degree in scientific discipline/Life Sciences or equivalent experience in the biotech or pharmaceutical industry
8+ years of relevant experience in a GMP and GXP environment with at least 3 years of demonstrated experience with the development, maintenance, and training oversight required
General knowledge of regulatory requirements for the pharmaceutical, biotechnology, or vaccine industry
Skilled in determining the state and needs of the learner and defining the end goal of instruction
Excellent interpersonal effectiveness, written/verbal communication, influencing, and negotiation skills
Ability to work independently
Excellent computer skills and advanced knowledge of Quality Systems
Direct experience with Quality Management Systems, Document Management Systems, Learning Management Systems, and Microsoft Office, including Word and Excel
Veeva experience required
Self-motivator with the ability to follow up on and complete multiple projects simultaneously

Job Responsibility

Develops, leads, and implements training initiatives that are aligned with business strategies
Design, develop and deliver instructional materials, both digital and physical, in an efficient, effective, appealing, engaging way
Manages the performance/effectiveness of quality system training programs
Work collaboratively on the GXP integrated digital landscape to support, resolve system technical issues and communicate best practices for electronic quality training systems
Assist in the refinement of system user training and support training delivery
Assist in improving and maintaining Beam’s overall Quality Management System (QMS), including policies and procedures, while keeping them current with emerging and changing regulations
Develops user requirements regarding Quality training systems and supports the generation/review/approval of computer system validation deliverables
Contributes to the generation, review, and approval of computer system test scripts
Support site and function audit preparations with respect to system functionality
Support development of harmonized/streamlined/standardized processes and supplemental documents (including Work Instruction creation or maintenance) governing management and usage of Quality Systems

Fulltime

New

Associate Director, IT Business Partnership, G&A

We are seeking a strategic and hands-on Associate Director, IT Business Partners...

Location

United States , Cambridge

Salary:

180000.00 - 220000.00 USD / Year

Beam Therapeutics

Expiration Date

Until further notice

Requirements

8+ years of experience in IT application management within a life sciences organization
Strong knowledge of SAP S/4HANA Finance modules (AP, AR, TRM, Financial Reporting, etc)
Led successful rollouts of SAP Analytics Cloud
Experience orchestrating middleware and API-based integrations with external systems (e.g., Coupa, ADP, JP Morgan, SuccessFactors)
At least one full implementation of SAP Financials, including cutover from legacy systems
Experience in SOX-compliant environments and audit support
Strong experience gathering requirements and translating them into solutions that meet business objectives
Proven experience managing third party vendor relationships and service delivery
Proven project management experience, including planning, execution, and stakeholder communication
Ability to work hands-on in operational support and troubleshooting

Job Responsibility

Responsible for the roadmap, budget, and lifecycle management of G&A applications including financial, legal, HR, and procurement systems
Lead selection and implementation efforts for new solutions in G&A portfolio in collaboration with business stakeholders and vendors
Provide hands-on operational support and troubleshooting for application portfolio and related integrations
Ensure SOX compliance and support audit activities related to IT controls
Partner with business stakeholders to maintain and enhance application portfolio
Manage vendor relationships and service delivery for third-party applications
Supervise and mentor a small team of IT professionals and/or contractors
Collaborate cross-functionally to align IT strategy with business goals

Fulltime

New

Senior Director, US Market Access Strategy

Beam is looking for a strategic leader to drive market access strategy for key B...

Location

United States , Cambridge

Salary:

250000.00 - 310000.00 USD / Year

Beam Therapeutics

Expiration Date

Until further notice

Requirements

Bachelor’s required, Master’s preferred with 18+ years of experience
10+ years of experience in US Pharma, including at least 5+ years in payer strategy / marketing or payer account management
At least 3+ years of experience working in cell & gene therapies required
Proven track record of successful collaboration with cross-functional teams
Substantial experience in shaping market access and pricing strategies, developing brand plans & payer marketing tools (value proposition decks), informing HEOR data strategies, supporting field market access teams, etc.
Previous product launch experience in buy-and-bill products
Excellent communication (written, verbal and presentation), interpersonal influencing and prioritization skills required with proven ability to influence across matrixed organizations including influencing without authority
Proven ability to operate independently and handle multiple projects with a high degree of initiative including project planning and prioritization of competing demands
Willingness to work with ambiguity and candor
Experience developing and managing promotional budgets and managing third-party vendors

Job Responsibility

Create and own near/mid/long term access strategies focused on optimizing pricing and coverage
Monitor coverage environment for gene therapies and competitive landscape and coordinate cross functionally to ensure alignment
Drive cross-functional access strategy synergies with broader brand strategy
Collaborate with future market access team members, such as field team, trade & distribution lead, government affairs lead, and patient services lead
Own market access component of brand level strategic plans, ensuring alignment to brand objectives as well as near/mid/long term market access objectives
Partner closely with Value Evidence Strategy (VES) lead to ensure value prop and customer materials are backed by evidence and aligned with Medical Affairs
Develop access journey for brand, highlighting critical access components including pricing/contracting, channel strategy, payer strategy, patient services, enterprise strategy, etc
Support insights development including conducting primary market research to support the market access strategy and tactical planning
Monitor & synthesize syndicated market research and external environment, impacting pharmaceutical delivery and reimbursement including industry trends, public policy, and competitive landscape

Fulltime

Licensed Practical Nurse/Registered Practical Nurse

Bayshore HealthCare

Location:
Canada

Category:
Nursing

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
December 23, 2025

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