Clinical Oncology Consultant Job at Remedium Partners (Greater London)

Clinical Genomics Scientist, Oncology

BillionToOne is looking for a Clinical Genomics Scientist, Oncology to help driv...

Location

United States , Menlo Park

Salary:

158401.00 - 179521.00 USD / Year

BillionToOne

Expiration Date

Until further notice

Requirements

Ph.D. in Human Genetics, M.S. in Genetic Counseling, or related field
2+ years of experience in somatic variant interpretation based on ACMG/AMP guidelines in a clinical setting (alternatively, 1+ years of germline variant interpretation and 1+ years of somatic variant interpretation experience)
Hands-on experience working with human mutation databases (COSMIC, ClinVar, OncoKB), functional annotation sources (dbSNP), and genome browsers (UCSC)
Familiarity with IGV and BAM file analysis and data-minded willingness to learn to use basic bioinformatics tools, with technically minded insights
Knowledge of cancer somatic mutation and signaling pathways (e.g., which mutations have FDA approved drugs, Phase II/III clinical trials, which mutations are considered “hot targets” for drug development, etc.)
Exceptional attention to detail to follow highly detailed SOPs and strong organizational skills to track and manage clinical reporting and product improvement projects
Excellent communication skills and ability to work collaboratively with cross-functional teams
Operationally-defined flexible schedule, including weekends, as dictated by clinical reporting needs

Job Responsibility

Somatic variant interpretation and data review: Perform somatic-based variant interpretation, diving into the literature and databases to classify variants and match treatments for reporting, performing verification as required with BAM file analysis
Clinical report drafting: Carefully draft reports for each requisition primarily using in-house reporting API, working closely with the engineering and QA teams on reporting, and the laboratory directors on report language
Somatic mutation interpretation and reporting policy development: Work closely with lab directors, R&D, medical, and other related functions to develop and modify the somatic interpretation SOPs in accordance with ACMG/AMP guidelines, and the latest published literature
Content curation: Contribute to curation of gene-level content such as domain and critical residue curation
Molecular tumor board: Serve as a subject matter expert in consulting with the medical science liaison team, and presenting in molecular tumor boards to facilitate knowledge sharing
Contribute to oncology R&D: Work closely with the R&D team to help with somatic oncology based projects, providing expertise on variant interpretation, biological pathways/mechanisms, and other gene/variant-level reviews and analyses

What we offer

Working alongside brilliant, kind, passionate and dedicated colleagues, in an empowering environment, toward a global vision, striving for a future in which transformative molecular diagnostics can help millions of patients
Open, transparent culture that includes weekly Town Hall meetings
The ability to indirectly or directly change the lives of hundreds of thousands patients
Multiple medical benefit options
employee premiums paid 100% of select plans, dependents covered up to 80%
Extremely generous Family Bonding Leave for new parents (16 weeks, paid at 100%)
Supplemental fertility benefits coverage
Retirement savings program including a 4% Company match
Increase paid time off with increased tenure
Latest and greatest hardware (laptop, lab equipment, facilities)

Fulltime

Director Business Development - Oncology

Fantastic opportunity to join TFS HealthScience! TFS HealthScience is a leading ...

Location

United States , Boston

Salary:

Not provided

TFS HealthScience

Expiration Date

Until further notice

Requirements

Bachelor’s Degree or equivalent relevant experience
Minimum of 5 years of experience in clinical research, business development, or sales within the CRO industry
Proven track record of at least 3 years in consultative sales with strong negotiation and closing skills
Strong communication skills with the ability to engage and influence clients and stakeholders at all levels
Deep understanding of clinical development and the regulatory landscape in the U.S.
Strong organizational skills, self-starter, and comfortable working independently in a remote environment
Experience with CRM tools and Microsoft Office Suite
Excellent presentation and proposal development skills
Willingness to travel across North America to attend client meetings, conferences and internal events as needed

Job Responsibility

Develop and execute a business development strategy focused on the North American biotech/pharma market
Drive new business acquisition to meet or exceed annual sales targets
Identify and qualify new leads, managing the full sales lifecycle from initial outreach to contract negotiation
Collaborate with internal teams to respond to Requests for Information (RFIs) and Requests for Proposals (RFPs)
Prepare TFS teams for client engagements, including Capabilities Presentations and Bid Defense Meetings (BDMs)
Manage contract and budget discussions post-award to ensure alignment and client satisfaction
Establish and maintain strong relationships with prospective and current clients
Organize and deliver high-quality sponsor presentations that communicate the value of TFS’ CDS services
Provide strategic input and leadership during proposal development
Monitor project status post-award and coordinate scope changes as needed

What we offer

competitive salary and performance-based incentives
comprehensive benefits
opportunity for personal and professional growth in a rewarding, global environment
Remote work flexibility
collaborative, mission-driven environment focused on patient outcomes and clinical innovation

Fulltime

New

Breast Oncologist

An excellent opportunity has arisen for a Consultant Medical Oncologist to join ...

Location

United Kingdom

Salary:

109725.00 - 145478.00 GBP / Year

Remedium Partners

Expiration Date

Until further notice

Requirements

Medical Degree (MBBS or equivalent)
Full GMC registration with a licence to practise
MRCP or equivalent qualification
Entry on the GMC Specialist Register in Medical Oncology (or within 6 months of CCT / CESR)
Minimum 1 year NHS experience
Experience in General Medical Oncology
Subspecialty experience in: Breast malignancies
Testicular and renal cancers
Experience delivering systemic anti-cancer therapy (SACT)
Evidence of clinical audit participation

Job Responsibility

Provide Consultant-level care in Medical Oncology, particularly: Breast malignancies (primary focus)
Testicular and renal cancers
Deliver systemic anti-cancer therapy (SACT) including: New patient assessment
Treatment planning
Review and follow-up clinics
Manage patients across outpatient clinics, MDT pathways, and inpatient care
Undertake oncology ward rounds and acute oncology input
Attend and contribute to weekly MDT meetings (Breast, Urology, and related tumour groups)
Work closely with: Oncology consultants
Specialist nurses

Fulltime

Medical/Clinical Oncologist - Consultant

An exciting opportunity has arisen for a Consultant in Medical / Clinical Oncolo...

Location

United Kingdom

Salary:

109725.00 - 145478.00 GBP / Year

Remedium Partners

Expiration Date

Until further notice

Requirements

Complete registration with the General Medical Council (GMC) with a licence to practise
Inclusion on the GMC Specialist Register (or eligibility within 6 months of interview)
CCT in Medical Oncology or equivalent (or evidence of equivalence for non-UK trained applicants)
Ability to independently manage complex oncology patients within multidisciplinary teams
Experience delivering radiotherapy and systemic anti-cancer therapy
Understanding of clinical governance, risk management, and oncology safety standards
Experience in teaching and supervision across professional groups
Evidence of engagement in clinical research and audit activity
Strong organisational, leadership, and IT skills
Minimum 1 year of NHS experience

Job Responsibility

Deliver consultant-led medical and clinical oncology services, including inpatient care, outpatient clinics, radiotherapy, and systemic anti-cancer therapy
Manage at least two tumour subspecialty areas, which may include breast, skin, haematological malignancies, gynaecological oncology, colorectal, urology, or lung cancer
Participate in multidisciplinary tumour boards, pre-clinic case discussions, and treatment planning meetings
Support acute oncology services, including immunotherapy toxicity management and emergency oncology pathways
Participate in on-call arrangements as agreed within the job plan
Maintain high standards of clinical documentation, patient safety, and professional practice
Participate actively in clinical trials and research activity, including principal investigator roles where appropriate
Support recruitment into local and national studies across radiotherapy and systemic therapy portfolios
Contribute to translational research and audit initiatives
Supervise and train junior doctors, clinical fellows, and multidisciplinary colleagues

Fulltime

Physician - Medical Oncology Geriatric Oncology

The University of Kansas Cancer Center (KUCC) is seeking a full time academic cl...

Location

United States , Shawnee Mission

Salary:

Not provided

The University of Kansas Health System

Expiration Date

Until further notice

Requirements

Seeking Physician-investigators at the Assistant/Associate Professor level (MD or MD/PhD)
Board certified/eligible in medical oncology or hematology/oncology, training in geriatric medicine, and eligible for licensure in Kansas
Proven ability to serve in a consultative capacity in geriatric oncology as well as manage a parallel subspecialty oncology practice, as well as conduct geriatric oncology clinical and/or translational research
Successful candidates will have demonstrated record of excellency in clinical care, originality and productivity in research, existing or potential for consistent extramural funding and an interest in graduate and medical education

Job Responsibility

Develop outpatient Geriatric Oncology assessment/consultative practice
Formalize and implement a Geriatric Oncology clinical program and research base
Conduct tandem subspecialty medical oncology clinical practice

What we offer

Recent increase in overall compensation package
Generous retirement contribution
Relocation assistance
Health, dental, vision insurance
CME allowance
LTD/STD and Life insurance
Professional liability insurance

Fulltime

Consultant Clinical Oncologist

An exciting opportunity has arisen for a Consultant Clinical Oncologist with a s...

Location

United Kingdom

Salary:

109725.00 - 145478.00 GBP / Year

Remedium Partners

Expiration Date

Until further notice

Requirements

Full GMC registration with a licence to practise
Fellowship of the Royal College of Radiologists (or equivalent)
Completion of higher specialist training in Clinical Oncology
Entry on GMC Specialist Register (or within 6 months)
Ability to run radiotherapy and SACT services for a major tumour site (Breast), plus another tumour site
Ability to provide expert clinical opinion and independent patient management
Strong communication and clinical decision-making skills
Commitment to teaching junior doctors and allied health professionals
Experience in clinical audit
Ability to organise clinical workload efficiently and manage administrative responsibilities

Job Responsibility

Deliver consultant-led outpatient oncology clinics and support patients receiving systemic anti-cancer therapy
Provide specialist Breast oncology services, including radiotherapy and SACT management, with flexibility for an additional tumour site
Support acute oncology pathways and contribute to the management of unplanned cancer care
Take ownership of a defined tumour-site workload and ensure evidence-based clinical practice
Participate in MDT meetings, peer review and multidisciplinary decision-making
Contribute to medical leadership, service innovation and development within oncology services
Supervise and train junior medical staff and SAS doctors
Actively engage in clinical audit, governance programmes and quality improvement initiatives
Participate in research activities and support innovative oncology practice
Undertake CPD, appraisal and professional development in line with Royal College guidance

Fulltime

Contractor, Market Strategy

Position at Vaniam Group. Contractor, Market Strategy. What You’ll Do: Leveragin...

Location

United States

Salary:

Not provided

Vaniam Group

Expiration Date

Until further notice

Requirements

Bachelor’s Degree
Minimum of one year of oncology work experience in pharmaceutical strategic planning/healthcare consulting
Good working knowledge of pharmaceutical and biotech industries
Ability to evaluate and extract relevant data from primary and secondary resources
Ability to quickly develop expertise in new therapeutic areas
Self-awareness and a service mindset with the ability to prioritize deep thinking, creativity, and collaboration
Ability to share opinions and challenge others in a respectful way
Ability and willingness to meet tight deadlines, multitask, and work within high-pressure situations
Fluency in MS PowerPoint and ability to prioritize, analyze, and synthesize clinical, financial, and other relevant data into succinct presentations aligned to business objectives

Job Responsibility

Leverage knowledge of the oncology marketplace and track emerging news and trends to provide clients with actionable insights and recommendations
Develop strategies for tumor and portfolio prioritization
Closely monitor changes in the market landscape and proactively communicate changes to stakeholders
Conduct landscape assessments and synthesize information about a given competitive therapeutic space
Propose innovative solutions to address client needs and translate insights into strategic recommendations
Employ strong communication skills to foster successful professional interactions
Other duties as assigned to drive deliverables and support client business objectives

Oncology Early-Stage Clinical Scientist

You will lead and coordinate the development of multiple studies of novel biolog...

Location

United States , Cambridge; La Jolla; Bothell; Groton; New York City

Salary:

176600.00 - 282900.00 USD / Year

Pfizer

Expiration Date

Until further notice

Requirements

Relevant PhD or PharmD and a minimum of 5 years of experience in a similar role in industry/CRO
MS and a minimum of 7 years of experience in a similar role in industry/CRO
BA/BS and a minimum of 10 years of experience in a similar role in industry/CRO
Clinical Research experience in Phase 1 in Oncology, on the side of the sponsor leading studies
Experience in or strong understanding of Oncology Drug Development especially in Early Development
Strong knowledge of clinical procedures, ICH guidelines, GCP and familiarity with FDA, EMA, and global regulations
Strong scientific writing skills and communication skills (written and verbal)
Clinical document writing experience (e.g., protocol, ICD, IB, IND), as well as understanding complex data analysis
Track record of scientific productivity as evidenced by publications, posters, abstracts and/or presentations
Experience working with and solid understanding of related disciplines, e.g., Clinical Operations, Data Management, Safety, Biostatistics, Regulatory, Study Management, Pre-Clinical, Pharmacology, Quality Assurance

Job Responsibility

Partner closely with the Global Development Lead (GDL) in the execution of the clinical development strategy and plan for the assigned molecule(s)/indication(s)
Responsible for scientific leadership and execution of clinical studies and delivering on innovative clinical study designs, high quality trial execution, safety assessment and interpretation of clinical study results
Support execution for all FIH programs through proof-of concept
Set the clinical data review strategy, ensure quality data and conduct review of emerging clinical data and trends
review and query data
present and discusse relevant data to appropriate teams, governance bodies, and other internal and external stakeholders
Conduct data review, analysis and interpretation of clinical trials data together with the GDL, Clinical Safety, and Biostatistics
Serve as technical resource for clinical issues raised by internal and external collaborators, investigators, consultants and contractors
Support and assist in the development of publications, abstracts, and presentations
May sit on project teams to support clinical development implementation and contribution to key development milestones, e.g. start-up and delivery of ESoE and PoC trials

What we offer

Eligibility for participation in Pfizer’s Global Performance Plan with a bonus target of 20.0% of the base salary
Eligibility to participate in our share based long term incentive program
401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution
Paid vacation, holiday and personal days
Paid caregiver/parental and medical leave
Health benefits to include medical, prescription drug, dental and vision coverage
Relocation assistance may be available based on business needs and/or eligibility

Fulltime

Clinical Oncology Consultant

Remedium Partners

Location:
United Kingdom , Greater London

Category:
Health and Beauty

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
January 05, 2026

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