Manage clinical projects from initiation through completion, coordinating cross‑functional activities, mitigating risks, and ensuring quality standards in a remote team environment.
Compensation
The expected salary range for this position based on the primary location of Arizona is 56,400.00 - 104,700.00 USD Annual. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance.
Responsibilities
Manage multiple clinical projects from initiation through completion, ensuring alignment with timelines, scope, and quality standards.
Serve as the primary point of contact for Pharma and Roche clients, ensuring clear communication and stakeholder alignment.
Coordinate project timelines and develop and execute project plans across CDx Pharma Services, aligning cross‑functional activities and tracking progress against defined milestones.
Identify and mitigate risks, gaps, and bottlenecks, driving solutions to maintain project timelines.
Oversee sample testing workflows and data reporting, ensuring accuracy, compliance, and adherence to quality standards.
Requirements
Bachelor’s Degree in Life Sciences, Clinical Research, Healthcare, or a related field
Master’s Degree or specialized training in Project Management or Clinical Research
Leadership of a team of Local Delivery Leads and delivery of clinical trials in specific therapy areas(TAs) and serving as a point-of-contact for cross-TA and cross-study issues.
Compensation
Germany Salary Range / Gehaltsbandbreiten Deutschland: EUR 85,500 to EUR 142,500
Responsibilities
Accountable for strong leadership, people management, talent retention and development within the Local Delivery Lead (LDL) Team in country.
Support and hold LDLs accountable to ensure all studies assigned to the LOC are delivered according to plan, with quality and within the agreed budget.
Responsible for working with the LDL to resolve and escalate issues that may impact study delivery.
Responsible for leading and developing the team of GSK LDLs by providing training, coaching, and mentoring including line and performance management.
Responsible for standardizing processes, identifying, and sharing best practices.
Requirements
University degree in Sciences (Medicine, Pharmacy, Biochemistry, Biology or related fields)
The Occupational Therapist is responsible for age appropriate interventions for the client that meet physical, emotional, developmental, psychosocial and educational needs to patients whom require rehabilitative care. The role involves delivery of high quality continuous care providing assessment, therapeutic exercises, education, and treatments in the patient's home.
Compensation
****Sign-on Bonus Option available****
Responsibilities
Access and manage patient’s rehabilitative needs utilizing general principles governing reasonable and necessary therapy
Manage patient from admission through discharge and appropriately schedule visits per MDs order
Perform routine occupational therapy procedures to meet the need of the patient
Develop the patient’s plan of care and revise it based on patient need within MD orders
Coordinate the care and services with the Clinical Supervisor and other team members and support services
Requirements
Graduate of an accredited school of Occupational Therapy
Coordinate and oversee federal relations projects, negotiate capacity funding and agreements, manage project lifecycles, and liaise with internal and external stakeholders to advance Musqueam’s strategic interests.
Responsibilities
Lead IGA projects and external negotiations
Represent Musqueam in environmental and impact assessment processes
Assist in negotiation strategy formulation
Document and advise on requirements for agreements
Engage in conflict and issue resolution
Requirements
Post‑secondary degree in Political Science, First Nations Studies, or related field
Nice to have: Experience with Environmental Assessments, Impact Assessments or permitting processes
Nice to have: Understanding of regulatory processes
Supports cross-functional collaboration to ensure Labeling and Artwork regulatory operational activities are planned, coordinated, and executed in a timely, accurate, and compliant way.
Responsibilities
Supports the preparation of high-quality labeling and artwork packages
Provides routine operational support to Country Regulatory Affairs, such as database maintenance and record filing
Engages with Global Labeling and Country/Regional Regulatory Affairs on labeling and artwork queries
Assists with process documentation updates and periodic revisions
Contributes to process improvement or simplification initiatives
Requirements
Bachelor’s degree or equivalent experience in life sciences, pharmacy, regulatory affairs, business, or a related field
Nice to have: Basic awareness of Regulatory Affairs
Lead strategy and execution of biologics drug substance programs at the Rahway, New Jersey site.
Compensation
$173,200.00 - $272,600.00
Responsibilities
Direct strategy and execution of biologics drug substance programs
Lead cross‑functional CMC teams
Coordinate strategy and execution across Drug Substance, Drug Product, Analytical Development, Regulatory Affairs, Quality Assurance, Global Supply Chain, pilot and commercial manufacturing, and external partners
Identify program risks and develop data‑driven contingencies
Maintain delivery rigor through structured meeting cadences and risk registers
Requirements
Ph.D. in Chemical Engineering, Biomedical Engineering, Pharmaceutics, Pharmaceutical Chemistry, Pharmaceutical Sciences, Chemistry, Biochemistry, Biology, or a related discipline
Seeking an accomplished scientific leader to direct the strategy and execution of biologics drug substance programs, combining cross-functional CMC program leadership with deep expertise in cell line, upstream, and downstream process development to advance biologics through First-in-Human (FIH) milestones.
Compensation
$173,000 - $272,600
Responsibilities
Lead assigned early-stage Development and Commercialization Teams (DCTs), with accountability for integrated CMC strategy, milestone readiness, and advancement through governance decisions.
Establish and lead matrixed CMC teams with clear structures, working groups, decision rights, timelines, escalation paths, and functional accountability.
Coordinate strategy and execution across Drug Substance, Drug Product, Analytical Development, Regulatory Affairs, Quality Assurance, Global Supply Chain, pilot and commercial manufacturing, and external partners.
Identify program risks, evaluate cross-functional trade-offs, develop data-driven contingencies, and provide clear recommendations to senior leaders and governance bodies.
Define phase-appropriate drug substance strategies covering cell line development, upstream and downstream process development, scale-up, technology transfer, and clinical supply.
Develop and implement advocacy and lobbying efforts relative to HP Inc’s priority federal issues.
Compensation
The base pay range for this role is $130,000 to $170,000 annually with additional opportunities for pay in the form of bonus and/or equity (applies to US candidates only).
Responsibilities
Develop, maintain, and implement strategies and policy positions in support of HP’s portfolio
Regularly interface with internal HP stakeholders to align on positions and advocacy plans
Anticipate the impact of government policies for the company
Identify proactive opportunities and develop related strategic plans
Create documents to brief company executives on legislative and regulatory matters
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Principal Scientist, Early DCT LeadMerck · Rahway, US