Clinical Lead - Oncology Job at Circle Health Group (Cheadle)

Lead Clinical Laboratory Scientist (CLS), Oncology

Join a team of brilliant, passionate innovators who wake up every day determined...

Location

United States , Menlo Park

Salary:

228788.00 USD / Year ▼

BillionToOne

Expiration Date

Until further notice

Requirements

Bachelor's degree in the chemical, physical or biological sciences
Minimum of 4 years of CLS experience in a clinical setting (molecular and/or high-complexity laboratory experience preferred)
A current California Clinical Laboratory Scientist License that meets requirements for Testing Personnel under CLIA regulations (42 CFR, part 493) (ASCP, CGMBS or generalist license is required)
Hands-on training and experience with manual molecular biology protocols, including DNA extraction, PCR, and automated liquid handlers
Advanced knowledge of Google Docs, Word, Excel, basic statistics and familiarity with LIMS systems and Next-Generation Sequencing
Strong attention to detail and ability to work flexibly and well under given timeframes.
Self-starter and dynamic team player with excellent verbal and written skills.

Job Responsibility

Lead clinical laboratory daily supervision in alignment with company values and mission
Hold General Supervisor delegation and responsibilities including oversight and support of day-to-day operations, scheduling, and troubleshooting
Manage CLIA direct reports including licensed and/or unlicensed staff (CLS, Clinical Laboratory Assistants)
Contribute to continuous process improvement projects including tech transfer, troubleshooting, training, and validations
Perform clinical laboratory assays to provide data for diagnosis, treatment, and prevention of disease
Perform quality control studies to ensure the accuracy of clinical data
Verify instrument performance by checking and calibrating specific lab instruments and documents data

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

Oncology clinical scientist intern

The Global Oncology Internship Program at Johnson & Johnson is a comprehensive l...

Location

Belgium , Beerse

Salary:

Not provided

Randstad

Expiration Date

January 25, 2026

Requirements

Legally/permanently authorized to work in Belgium with no required sponsorships
Must be currently enrolled in an accredited University or College program throughout the duration of the internship
Must not be graduating before, during, or after the start or end of the internship program
Currently enrolled in biology, cell/molecular biology, chemistry, pre-med, nursing program, public health, biochemistry, biomedical engineering, oncology, clinical pharmacology, clinical or translational research, computational biology, precision medicine, or similar areas of study
Undergraduate students with completion of a minimum of four semesters at program start or graduate students are eligible
Minimum cumulative GPA of 3.0
Students in good standing, working towards the completion of an undergraduate or graduate degrees
Graduate students must be pursuing a master’s, PharmD, Physician Assistant or PhD or other clinical related degrees
Self-motivated, future scientist leaders passionate about drug development and clinical research
Detailed oriented with good organizational skills

Job Responsibility

Gaining overall understanding of clinical research and drug development including but not limited to Good Clinical Practices (GCPs), International Conference of Harmony (ICH) guidelines, and Standard Operating Procedures (SOPs)
Attend “Bench to Bedside” Lecture Series to gain knowledge of the drug development process and clinical research
Assisting with management of trial activities including patient tracking through screening process, and eligibility/enrollment reviews
Assisting with document processing and management within the electronic master file (i.e., vTMF)
Participating in department and team meetings
Participating in cross-functional team and clinical team meetings
Developing study training materials/documents
Shadowing key clinical and or functional roles for learning/development opportunities
Observing Site Initiation Visit (SIV) Meetings (if applicable for assigned projects)
Supporting Clinical Team with study start up activities during trial set up, and other study tasks during conduct, and close out (depending on the stage of the trial)

What we offer

We offer an inclusive work culture that is open, innovative, and performance driven

Fulltime

!

Vice President of Medical Affairs and Clinical Development, Oncology

We are hiring a Vice President of Medical Affairs, Oncology to lead the executio...

Location

United States , Menlo Park

Salary:

269282.00 - 290402.00 USD / Year

BillionToOne

Expiration Date

Until further notice

Requirements

M.D. degree required
must be a board-certified Medical Oncologist
M.D./Ph.D. strongly preferred
5+ years of leadership experience in medical affairs and clinical development within oncology
Proven track record of designing and executing clinical studies for diagnostics and/or therapeutics
Deep knowledge of medical education, payer evidence requirements, and regulatory expectations
Exceptional scientific communication and cross-functional leadership skills
Thrives in fast-paced, entrepreneurial environments

Job Responsibility

Lead the MSL function to drive provider engagement, medical education, and scientific communications in support of commercial and access efforts
Design and execute clinical trials that generate robust evidence for guideline inclusion, regulatory milestones, and payer coverage
Oversee the generation of clinically actionable insights and high-impact publications based on study and real-world data
Collaborate closely with Product, Commercial, R&D, Market Access, and Regulatory teams to ensure that medical strategy supports business outcomes
Hire, mentor, and develop high-performing leaders across the medical, clinical, and translational teams

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

Clinical Practice Specialist, Inpatient Oncology

The Clinical Practice Specialist (CPS) is a member of the nursing leadership tea...

Location

United States , Boston

Salary:

129800.00 - 148400.00 USD / Year

Dana-Farber Cancer Institute

Expiration Date

Until further notice

Requirements

Master of Science in Nursing required
Clinical Nurse Specialist track is preferred
Current RN license in Massachusetts (compact licensure) language
3 years of oncology nursing experience and 3 years of oncology experience
Expertise in oncology nursing standards and evidence-based practice required
Oncology-specific certification required within 3 years of hire
Strong communication and interpersonal skills
Excellent organizational and time management abilities
Proficiency in educational technology and software
Ability to mentor and guide nursing staff effectively

Job Responsibility

Models excellence in nursing practice using scientific knowledge and advanced concepts in the assessment, diagnosis, planning, implementation and evaluation of actual or potential problems in the oncology patient population
Collaborates and consults with nurses and other to influence nursing practices and improve care outcomes within a patient population
A key stake holder and decision maker for the development, implementation and evaluation of standards of care, policies, guidelines, the introduction of new equipment, technology, and practices at the point of care and the integration of EBP into daily operational activities
Maintains expertise in ONS, ASCO, and other professional nursing standards and stays current on oncology evidence and changes in disease and treatment practices
Participates in local and national professional activities and organizations to promote the educational and professional growth of self and others within DFCI and the community
Provides content expertise as needed
Collaborates with Professional Development Specialist on curriculum development based on Learning Needs Assessment results
Contributes to the creation of an environment that stimulates continuous self-learning, positive group processes, reflective practice, and the empowerment of others
Models constructive and mutually respectful relationships with colleagues
Fosters an environment that is sensitive to the needs of diverse populations, including but not limited to culture, ethnicity, gender, and age

Fulltime

Laboratory Director/Senior Laboratory Director - Oncology

We are seeking an experienced and highly skilled Molecular Genetics Clinical Lab...

Location

United States , Menlo Park

Salary:

216481.00 - 264002.00 USD / Year

BillionToOne

Expiration Date

Until further notice

Requirements

Doctoral degree (PhD, MD, or equivalent) in genetics, molecular biology, or a related field
Board certification (ABMGG, ABP in Molecular Genetic Pathology, or equivalent)
Valid or eligible for California Clinical Laboratory Director license (CGMB, CGMBS, MD/DO licensure) and New York State CoQ in oncology testing
4+ years in a regulated clinical laboratory environment (CLIA/CAP/NYSDOH), with at least 3 years in molecular oncology testing including NGS
Proven leadership in developing, validating, and implementing oncology assays (e.g., somatic mutation panels, methylation assays)
Deep knowledge of cancer genomics, including tumor heterogeneity, somatic driver mutations, and targeted therapies
Experience with variant interpretation databases (COSMIC, OncoKB, ClinVar), IGV, BAM file review, and molecular tumor board participation
Strong analytical, communication, and organizational skills, with a track record of leading teams in high-growth environments
Proficiency with LIMS and oncology-focused bioinformatics tools

Job Responsibility

Provide technical oversight to ensure high-quality oncology testing and alignment with laboratory and clinical goals
Interpret somatic variant results from Northstar liquid biopsy assays, classify variants, and sign out oncology clinical reports
Troubleshoot technical issues related to oncology workflows, including liquid biopsy sample prep, NGS library preparation, sequencing, and data analysis
Evaluate lab performance, implement process improvements, and promote robust quality assurance systems
Review Non-Conforming Events and CAPAs to ensure timely resolution of issues impacting oncology test performance
Ensure compliance with CLIA, CAP, NYSDOH, and other applicable regulatory standards for oncology assays
Oversee accurate documentation of SOPs, validation reports, QC records, personnel competencies, proficiency testing, and report archives
Collaborate with bioinformatics, R&D, and medical affairs on assay development, interpretation guidelines, and continuous assay optimization
Participate in budget planning and manage lab expenses to ensure financial efficiency while maintaining exceptional quality
Support special projects, including scaling new oncology tests, preparing for inspections, and implementing automation

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

Freelance Senior Clinical Research Associate

TFS HealthScience is a leading global, mid-size Contract Research Organization (...

Location

Salary:

Not provided

TFS HealthScience

Expiration Date

Until further notice

Requirements

Bachelor’s degree, preferably in life sciences or nursing, or equivalent
Minimum of 2 years of experience working as a CRA (in oncology)
Ability to work in a fast-paced environment with changing priorities
Understanding of basic medical terminology and science related to assigned drugs and therapeutic areas
Solid understanding of Good Clinical Practice (GCP) regulations and ICH guidelines
Ability to work independently and within a team/matrix organization
Excellent written and verbal communication skills
Strong organizational skills
Ability and willingness to travel

Job Responsibility

Monitor clinical trials on-site and remotely in accordance with TFS/client SOPs, FDA regulations, and GCP/ICH guidelines
Review CRFs (paper or electronic) and subject source documentation for validity and accuracy
generate queries to resolve data issues
Identify site problems or deficiencies and report them to management through trip reports, memos, and communication with the Project Manager or Lead CRA
Initiate corrective actions as directed by the supervisor
Contribute to Ethics Committee/IRB application submissions and prepare required documentation in collaboration with the CTA and as directed by the Lead CRA/Project Manager
Participate in contract handling and negotiation under direction of the Lead CRA/Project Manager
Set up the Investigator Site File (ISF) and Study Master File (SMF), or support the CTA in doing so, and distribute materials to investigational sites
Collaborate with the study team on SMF maintenance
Order, ship, and reconcile clinical investigational supplies for study sites, if applicable

What we offer

competitive compensation package
comprehensive benefits
opportunity for personal and professional growth in a rewarding environment

Parttime

Oncology Nurse Manager

Oncology Nurse Manager role for an Oncology Day Unit within an award-winning hea...

Location

United Kingdom , Guildford

Salary:

60000.00 - 64500.00 GBP / Year

Compass Associates

Expiration Date

Until further notice

Requirements

Qualified Nurse with NMC registration
Right to Work in the UK
Strong clinical experience working within an Oncology setting
SACT (Systematic Anti-Cancer Therapy) passport
Experience in leading multidisciplinary teams and supervising clinical staff
Solid understanding of clinical governance, audits, infection prevention and risk management
Excellent communication, leadership and organisation skills
Passion for high quality care

Job Responsibility

Oversee the running of the Oncology Day Unit, ensuring smooth and effective operations
Provide expert clinical oversight of oncology care, from diagnosis and treatment, to end of life support
Inspire, mentor and develop the nursing team, fostering a culture of education, compassion and inclusion
Drive service development, implementing policies and strategies to enhance patient experience and outcomes
Build and maintain strong relationships with consultants, senior colleagues, the wider multidisciplinary team and patients

What we offer

Free Parking
Private Medical Insurance
CPD
Season Ticket Loan
Free parking
Excellent work-life balance
Life assurance
Free gym membership with discounts for family members
Free access to GPs
Wellbeing hub

Fulltime

Clinical Lead - Oncology

Circle Health Group

Location:
United Kingdom , Cheadle

Category:
Nursing

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
January 12, 2026

Expiration:
February 08, 2026

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