Lead, Oncology Field Excellence and Operations Job at GSK (Durham)

Director, Oncology Field Medical Excellence, Strategy and Operations

The Field Medical Excellence, Strategy, and Operations Director will drive strat...

Location

United States

Salary:

Not provided

GSK

Expiration Date

Until further notice

Requirements

MS, RN, PharmD, PhD or equivalent post-graduate degree, MBA or equivalent experience
4 + years of pharmaceutical industry experience, including field-based experience in Medical Affairs
Experience leading significant change initiatives leveraging advanced project management skills
Must be US-based for consideration

Job Responsibility

Ensure frameworks and operational elements are in place to support execution and monitoring of key initiatives (e.g., FMEP framework, medical unmet need, congress framework)
Partner with field leaders to identify medical capability needs and deliver timely innovative solutions to enhance skills and competencies, supporting continuous improvement in MSL engagement strategies, ensuring best-in-class scientific impact, high-quality engagement, and insights generation
Provide training to bolster proficiency across field medical systems and foster digital fluency, enhancing productivity and effectiveness (GenAI tools, Veeva CRM, PowerBI etc.)
Continually evaluate and refine best-in-class processes, implementing new innovations and technologies to simplify complex procedures and drive performance for field medical teams
Oversee the maintenance and creation of systems (dashboards, analytical tools, Veeva CRM, etc.) for evaluating customer interactions, tracking progress towards goals, and enabling leadership teams to assess and coach performance
Oversee the operational execution of Field Medical Plans to ensure alignment to scientific exchange policies and processes, including support of audit/monitoring activities
Serve as the first point of escalation for field leadership, ensuring policies/guidance are applied prior to escalation, communicate governance and compliance related issues to the leadership team, and support audit/monitoring activities for OFM
Collaborate effectively with medical matrix partners, including US Medical Affairs Leads (USMALs), Medical Directors, MSL Directors, and Medical Communication and Scientific Training Directors, to deliver on responsibilities within the role
Responsible for supporting budget process for key field activities
Ability to travel 15 to 20%

What we offer

Competitive base salary
Annual bonus based on company performance
Flexible working options available for most roles
Learning and career development
Access to healthcare & wellbeing programmes
Employee recognition programmes

Fulltime

Director Nursing Oncology Center

We are offering to qualified and experienced candidates a sign-on bonus not to e...

Location

United States , Santa Maria

Salary:

72.88 - 108.42 USD / Hour

American Nursing Care

Expiration Date

Until further notice

Requirements

Bachelor's Degree in Nursing (e.g. BSN) or equivalent education and experience and Master's degree in nursing or other-related field (e.g., MSN/MBA/MHA) required
Minimum of three (3) years of nursing experience required
Minimum two (2) years of leadership experience required
Registered Nursing License (RN) in CA required
Basic Life Support (BLS) required

Job Responsibility

Lead the Medical Oncology practice and support the day to day operations of our Oncology Clinic
Drive to develop, continually improve and promote quality standards of care while ensuring an excellent patient experience
Responsible for the financial management of the clinic
Partner with Philanthropy to assist with developing funding opportunities for oncology services

What we offer

Sign-on bonus
Relocation assistance
Annual performance-based bonus program
Annual employer contribution to retirement program (no employee contribution needed)
Medical benefits for the employee at no payroll deduction
23 days PTO accrued annually
12 days Sick Leave accrued annually

Fulltime

Director, Clinical Pharmacology

The role is positioned in the Clinical Pharmacology group, Clinical and Quantita...

Location

United States , Cambridge

Salary:

167000.00 - 300700.00 USD / Year

Moderna

Expiration Date

Until further notice

Requirements

PhD and/or PharmD in Clinical Pharmacology, Pharmacometrics, Pharmaceutics, Statistics, Engineering, or a related field with a minimum of 8-10 years of industry experience in clinical pharmacology
In depth knowledge of clinical pharmacology, PK/PD principles, modeling and simulation, ADME and quantitative translational sciences
Hands-on quantitative skills, modeling expertise and familiarity with clinical operations and translational sciences
Sound knowledge of drug regulatory authority biopharmaceutics and clinical pharmacology requirements to support the clinical development and marketing of new drug products
Drug development experience in oncology and rare diseases preferred
expertise in immune therapeutics and/or infectious diseases is a plus
Platform expertise in mRNA therapeutics, and/or experience with biologics and new modalities preferred
Demonstrated ability to work independently, lead functional initiatives, adapt quickly and collaborate effectively in a highly dynamic environment and influence cross-functional teams
Proficient in using pharmacokinetic, modeling and data visualization software (e.g. Phoenix WinNonlin, R, Monolix, NONMEM, etc)
Outstanding verbal and written communication skills, with the ability to distill complex data for diverse audiences

Job Responsibility

Develop a fit-for-purpose Clinical Pharmacology development plan, including dose selection and optimization, evaluation plan for special populations, PK/PD and immunogenicity assessment, and pediatric development
Collaborate with program teams to develop dose selection strategy and support decision makings for first-in-human studies and IND submissions
Represent CQP in a highly matrixed team setting to drive study execution and operational excellence toward product development goals
Lead the development of CQP related sections in regulatory documents (e.g., clinical protocols, INDs, regulatory meeting briefing books, summary documents for BLAs, responses to regulatory authorities) and represent clinical pharmacology in regulatory interactions
Lead/oversee the Clin Pharm data analysis, interpretation, and reporting to inform clinical implications and development decisions
Advocate and represent clinical pharmacology and MIDD strategies with internal and external stakeholders
Mentor junior team members to contribute to the development of a high-performing Clinical Pharmacology team
Leverage literature data and collaborate with external consultants, CRO partners and academic sites to problem solve and develop solutions to clinical pharmacology issues and grow organizational knowledge on mRNA platform

What we offer

Best-in-class healthcare coverage, plus voluntary benefit programs to support your unique needs
A holistic approach to well-being, with access to fitness, mindfulness, and mental health support
Family planning benefits, including fertility, adoption, and surrogacy support
Generous paid time off, including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
Savings and investment opportunities to help you plan for the future
Location-specific perks and extras
Annual discretionary bonus, other incentive compensation, or equity award

Fulltime

Lead Medical Operations Manager

The Medical Operations Manager, Poland at Exact Sciences works closely with the ...

Location

Poland , Warsaw

Salary:

Not provided

Exact Sciences

Expiration Date

Until further notice

Requirements

Ph.D. in Medical / Pharmaceutical or Health Science / or field as outlined in the essential duties
4-6 Years of industry experience (working in medical affairs - pharma/biotech/med tech)
Proven record of working in matrix environment and delivering as part of a cross-functional remote team
Solid track record of multi-project management and execution
Knowledge of IT Systems including VEEVA advantageous
Knowledge of building and tracking complex financial budgets
Excellent oral, written and presentation communication skills
Excellent English, multiple languages preferred
Ability to independently deliver quality results in a timely manner
Track record of delivering innovative Medical activities across markets

Job Responsibility

Leads the delivery of International Medical Governance model & meetings
Delivers monthly balanced scorecard for International Medical
Secures the integration of the different IT systems to Medical International
Leads the grant & donations processes
Identifies, leads and executes process initiatives across the medical organization
Leads and delivers the strategy for onboarding of all new Medical employees
Works closely with CMO to help prepare presentations and reports
Leads the budgeting and finance tracking for all Medical spend across the region
Owns and manages the international congress attendance strategy
Leads and owns the medical planning process

Fulltime

Lead Clinic Medical Technologist

Lead Clinic Medical Technologist - Full Time - First Shift. Acts as a resource a...

Location

United States , Burlington; Kenosha; Mount Pleasant

Salary:

30.70 - 46.05 USD / Hour

Advocate Health Care

Expiration Date

Until further notice

Requirements

Medical Technologist (MT) certification issued by the American Society for Clinical Pathology (ASCP)
Medical Laboratory Scientist (MLS) certification issued by the American Society for Clinical Pathology Board of Certification (ASCP BOC)
Medical Technologist (MT) certification issued by the American Medical Technologists (AMT)
Bachelor's Degree in Clinical Laboratory Sciences
Bachelor's Degree in Medical Technology or related field
Typically requires 2 years of experience in a laboratory related position
Excellent verbal, written and interpersonal communication skills
Ability to handle stressful situations in a calm and professional manner
Ability to work a flexible schedule, which may include alternate site assignment
Maintains patient confidentiality in and out of the workplace

Job Responsibility

Acts as a resource and role model to employees, which includes training/orienting and providing day-to-day work direction
Assigns, monitors, and reviews progress and accuracy of work, monitors productivity, maintains appropriate staffing levels, directs efforts and provides guidance on more complex issues
Assists with human resource responsibilities, which may include interviewing and selection of new employees, staff development, resolution of employee concerns, and employee morale
Assists in interpreting department policies and procedures, and advises and updates staff on procedural changes
Assists with preparation and monitoring of operating and capital budgets
Performs all duties of the technical and/or support staff
Serves as staff resource regarding technical and/or administrative policies and procedures
Participates in policy/procedure review process
Documents all appropriate information for quality assurance/improvement according to established protocol
Utilizes laboratory information systems appropriately

What we offer

Paid Time Off programs
Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability
Flexible Spending Accounts for eligible health care and dependent care expenses
Family benefits such as adoption assistance and paid parental leave
Defined contribution retirement plans with employer match and other financial wellness programs
Educational Assistance Program
Premium pay such as shift, on call, and more based on a teammate's job
Incentive pay for select positions
Opportunity for annual increases based on performance

Fulltime

Hematology Oncology Commercial Lead

The Oncology team is looking for a Commercial Director who will lead the commerc...

Location

Japan , Tokyo

Salary:

Not provided

Pfizer

Expiration Date

Until further notice

Requirements

Extensive experience developing and implementing pharmaceutical business strategy
Experiences in building high performing team that includes Customer Facing team
Experience in leading and developing talents to achieve the aspirational goals
Experience in developing and implementing omnichannel marketing strategy
Proven track record of leading projects, driving changes, and organizing teams that successfully achieve milestones and deliverables
Experience working in multiple cultures and demonstrated ability to work effectively across cultures
Strong competency in commercial strategy and execution
Excellent financial acumen in addition IT literacy for forecasting and business case development
Knowledge of pharmaceutical and healthcare industry and external environment
Strong track record of compliance, integrity

Job Responsibility

Strategic Planning and Execution: Lead all aspects of strategic brand planning and commercial management, delivering strategies and executing tactics to achieve financial budget (revenue and IBT in Operating Plan) for the portfolio
Strategic Prioritization : Make trade-off decisions to prioritize focus areas and spend investment to maximize brand and launch performance
Organizational Leadership: Lead, mentor, and manage a team of marketing talents and customer-facing colleagues, fostering a culture of collaboration, innovation, and excellence
Executional leadership of Customer Facing Team: Mobilize customer facing team (HSP) with clear KPI and execution guidance (e.g. allocation, segmentation & targeting) to ensure impactful execution in the field
Omni-channel strategy : Lead the development and execution of Brand Plans, including developing robust omnichannel strategies and content to meet customer needs, optimize patient outcomes and maximise brand opportunities and values
Shaping external market landscape : Proactively shape the market for new launches and navigate the external uncertainty
Cross functional leadership: Partner and collaborate with relevant Global & ICO teams and locally with sales, P&HE, ISE and cross functional to deliver the outcomes
Financial accountability: Partner with Finance to develop business forecasts and regularly track performance against budget targets
Integrity: Partner with medical affairs, regulatory, legal and compliance to ensure strict adherence to promotional guidelines and 100% compliance with all law, regulation, SOP, internal or external rule/policies

Fulltime

Senior Commercial Consultant - Life Sciences

We’re looking for experienced professionals to join our dynamic team, spanning C...

Location

United States , Boston; New York

Salary:

124100.00 - 226200.00 USD / Year

PA Consulting

Expiration Date

Until further notice

Requirements

Bachelor’s or Master’s degree in Business, Biology, Pharmacology, or a related field
3+ years of Consulting experience in the biotechnology, pharmaceutical, or life sciences with expertise in at least one of the following: Brand strategy, Commercial, Pricing and market access, Commercial operations model transformation, Digital campaign management strategy
Strong commercial strategy with a focus on the US market dynamics, including knowledge of IRA, Medicare, Medicaid
Proven experience in primary research, conducting interviews, and managing quantitative surveys within the life sciences industry
Expertise in pharmaceutical datasets (e.g., pricing, prescription, claims databases) and proficiency in Excel
A demonstrated ability to lead teams, manage client relationships, and deliver strategic insights that drive value

Job Responsibility

Lead and support client engagement teams, delivering high-quality solutions across commercial strategy, product launch, marketing, and business transformation for life sciences clients
Manage and execute key workstreams in large-scale client projects, ensuring project milestones and outcomes are met
Provide strategic insights and solutions in areas including commercial strategy, product launch, marketing, and analytics
Contribute to fostering a collaborative, innovative, and inclusive work environment, mentoring and developing junior team members
Build and nurture long-term client relationships, expanding networks across PA Consulting and client organizations
Stay current with industry trends, emerging technologies, and innovations in life sciences, commercial operations, and analytics

What we offer

Group medical insurance
Health Savings Account with company match
Teladoc and informed Nurse line resources
Long term care plan
Group dental insurance
Vision plan
401(k) Savings Plan with company profit sharing contribution
Commuter and Parking tax-savings benefit
15 days paid vacation days with the opportunity to buy five additional days
10 paid Holidays plus 10 paid sick days

Fulltime

New

Senior Clinical Research Associate

Senior Clinical Research Associate, FSP Model, Paris, Hybrid or Home based, Prod...

Location

France , Paris

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

Advanced degree in a relevant field such as life sciences, nursing, or medicine
Extensive experience as a Clinical Research Associate (4/5 years independent monitoring or more), with a proven track record of managing complex trials within a CRO or Pharma environment
Fluency in French and professional proficiency in English (mandatory for reporting and international stakeholder management)
In-depth knowledge of ICH-GCP guidelines
Proven ability to manage multiple high-priority sites and projects simultaneously, with superior organizational and problem-solving skills
Excellent communication and interpersonal skills, with the ability to influence site compliance and represent a leading global sponsor effectively
Ability to travel as required to clinical sites and should possess a valid driver's license

Job Responsibility

Independently monitor Phase II–IV clinical trials as a senior resource dedicated to a major French pharmaceutical leader, ensuring full compliance with ICH-GCP and specific sponsor SOPs
Manage clinical studies in France across multiple complex therapeutic areas including Neurology, Rare Disease, Dermatology and Oncology
Lead site qualification, initiation, monitoring, and close-out visits, providing expert oversight and ensuring the highest standards of site performance
Ensure protocol compliance, data integrity, and participant safety through rigorous source data verification and proactive site management
Build and maintain influential relationships with investigators and site personnel to drive recruitment and facilitate smooth trial operations within this exclusive partnership
Perform advanced data review and resolution of complex queries to maintain the highest quality of clinical data within the sponsor’s proprietary systems
Contribute to the preparation, review, and optimization of study documentation, including monitoring plans and clinical study reports
Oversee study documentation, regulatory submissions, and ethics/IRB approvals to ensure strict adherence to trial timelines
Drive study cost efficiency and provide proactive resolution for site-level issues to meet critical milestones for our pharmaceutical partner

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, Oncology Field Excellence and Operations

GSK

Location:
United States , Durham ▼
Philadelphia

Category:
IT - Administration

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
March 27, 2026

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