Clinical Scientist Job at CARE Fertility (Northampton)

Clinical Scientist

As a Clinical Embryologist, you’ll play a vital role in all aspects of laborator...

Location

United Kingdom , Manchester

Salary:

43645.00 - 46690.00 GBP / Year

CARE Fertility

Expiration Date

Until further notice

Requirements

HCPC-registered
ICSI-trained Clinical Embryologist
passionate about delivering outstanding care
understands the vital role of the laboratory in the patient journey
Biopsy experience preferred
professionalism
curiosity
compassion

Job Responsibility

oocyte collection
sperm preparation and freezing
insemination and ICSI
fertilisation and embryo assessment
embryo freezing and transfer
oocyte cryopreservation
biopsy (if trained)

What we offer

Competitive salary
33 days annual leave (inc. public holidays)
Pension scheme
Life assurance
retail discounts
wellbeing hub
holiday trading
internal training programmes
funded external courses
clear path for career progression

Fulltime

Clinical Scientist

At Care Fertility, you'll join a welcoming, forward-thinking team that values co...

Location

United Kingdom , Leeds

Salary:

43645.00 GBP / Year

CARE Fertility

Expiration Date

Until further notice

Requirements

HCPC registered
ICSI-trained Clinical Embryologist
passionate about delivering outstanding care
understands the vital role of the laboratory in the patient journey
professionalism, curiosity, and compassion

Job Responsibility

oocyte collection
sperm preparation and freezing
insemination and ICSI
fertilisation and embryo assessment
embryo freezing and transfer
oocyte cryopreservation
biopsy (if trained)

What we offer

Competitive salary
33 Days annual leave (inc. public holidays)
Pension scheme
Life assurance
Retail discounts
Wellbeing hub
Holiday trading
Internal training programmes
Funded external courses
Clear path for career progression

Fulltime

Clinical Scientist

This role exists to in our clinical team. If you are a scientific problem solver...

Location

United States , Trumbull

Salary:

59300.00 - 88900.00 USD / Year

Unilever

Expiration Date

Until further notice

Requirements

BS in pharmacy, biology, biochemistry, chemistry or related fields
Flexibility and open mindedness in achieving objectives as well as rapidly responding to changing priorities
Ability to work well in teams and demonstrate the ability to collaborate with others
Ability to work independently, problem solving, communication and organizational skills
Attention for details and critical thinking

Job Responsibility

Design and execute clinical studies to support Personal Care R&D programs
Work in partnership with third-party vendors to guarantee complete and timely deliveries
Responsible for product efficacy evaluation of skin cleansing products through the design, execution, and analysis of human clinical trials
Responsible for the study coordination for in-house & external studies in compliance with internal and external regulations
Must have working-knowledge in data collection & technical interpretation, designing & executing experiments, basic statistics understanding, technical problem-solving skills and excellent technical writing skills
Responsible for successfully delivering communication of study results to stakeholders

What we offer

Bonus eligible
Long-Term Incentive (LTI) eligible
Eligible to participate in our benefits plan
Health insurance (including prescription drug, dental, and vision coverage)
Retirement savings benefits
Life insurance and disability benefits
Parental leave
Sick leave
Paid vacation and holidays
Access to numerous voluntary benefits

Fulltime

Clinical Scientist

A Clinical Scientist is a healthcare professional who uses their scientific know...

Location

Salary:

Not provided

KGTiger

Expiration Date

Until further notice

Requirements

Master’s degree in a relevant scientific discipline, such as biochemistry, molecular biology, or immunology
2-3 years of experience in a clinical laboratory setting
Excellent knowledge of laboratory techniques and procedures
Strong analytical and problem-solving skills
Excellent written and verbal communication skills
Strong understanding of clinical research principles and practices
Excellent research skills
Ability to work independently and as part of a team

Job Responsibility

Design and conduct clinical research studies
Analyze data and publish findings
Supervise research staff
Collaborate with other scientists
Stay up-to-date on the latest clinical research

Lead Data Scientist - Clinical Informatics (Clinical Data Standards)

We’re building a world of health around every individual — shaping a more connec...

Location

United States , New York

Salary:

130295.00 - 260590.00 USD / Year

CVS Health

Expiration Date

June 29, 2026

Requirements

7+ years of relevant experience in clinical informatics, healthcare analytics, or clinical data management
Deep expertise in clinical data types and structures, including CCD data, lab results, clinical notes, and administrative healthcare data
Strong knowledge of clinical coding systems and terminologies, such as ICD-10, CPT, HCPCS, SNOMED-CT, LOINC, NDC, and RxNorm
Experience designing and documenting data models, taxonomies, or classification frameworks for clinical or healthcare data
Proven ability to enable and support downstream data consumers (analysts, data scientists, business users) through documentation, training, and consultative support
Experience leading cross-functional projects from concept to delivery by coordinating across clinical, technical, and business stakeholders
Proficiency with SQL and experience working with large-scale healthcare datasets
Experience using cloud-based data platforms, preferably Google Cloud Platform (GCP) tools including BigQuery, for querying, transforming, and managing data
Strong understanding of data quality principles, including validation, profiling, and monitoring of healthcare data
Excellent written and verbal communication skills, including the ability to explain complex clinical data concepts to both technical and non-technical audiences

Job Responsibility

Serve as a subject matter expert in clinical data, including CCD data, with deep understanding of how to structure and apply this data to solve healthcare problems
Design and maintain clinical data models, taxonomies, and classification frameworks that enable consistent interpretation and use of clinical data across the organization
Develop and govern the clinical data feature store, establishing standards, documentation, and best practices that accelerate adoption of clinical data for downstream analytics, reporting, and AI/ML use cases
Enable self-service analytics by building well-documented, validated, and reusable data assets (tables, views, features) that empower analysts and data scientists to work independently with clinical data
Create and maintain comprehensive data documentation, including data dictionaries, lineage, business logic, known limitations, and appropriate use guidelines for clinical datasets
Build queries, dashboards, and data visualizations to effectively communicate data quality metrics, data availability, and clinical insights to technical and non-technical stakeholders
Partner with clinical, operational, and business stakeholders to understand their data needs, translate requirements into data solutions, and ensure clinical data assets meet their analytical objectives
Lead and mentor data scientists, data analysts, and data engineers, providing guidance on clinical data interpretation, appropriate use, and best practices for working with healthcare data
Establish data quality frameworks for clinical data, including validation rules, anomaly detection, and monitoring processes to ensure data integrity and reliability
Translate clinical concepts into analytical frameworks, ensuring that business partners understand the capabilities and limitations of available clinical data

What we offer

Medical, dental, and vision coverage
Paid time off
Retirement savings options
Wellness programs
CVS Health bonus, commission or short-term incentive program
Award target in the company’s equity award program

Fulltime

New

Clinical Scientist Associate Director – Late Development, Oncology

Join Amgen's Mission of Serving Patients. At Amgen, if you feel like you're part...

Location

Portugal , Lisbon

Salary:

79656.90 - 107771.10 EUR / Year

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree and 3 years of life sciences/healthcare experience
Master's degree and 5 years of life sciences/healthcare experience
Bachelor's degree and 7 years of life sciences/healthcare experience

Job Responsibility

Support set up and execution of late phase clinical trials with a focus on data quality
Assist in authoring clinical protocols, Investigators Brochures and other regulatory documents ensuring consistency and clarity
Provide input into and implementation of data management plan, CRF design, and data review oversight
Support review, analysis, and presentation preparation of clinical trial data for internal decision making, external interactions, and regulatory submission
Assists the management of collaborators, consultants, and/or Clinical Research Organizations in completion of key projects
Anticipate and actively manage problems across a broad spectrum of cross-functional teams
Work cross-functionally within teams to ensure clinical strategy is translated into the development of the study concept document, study protocol and related documents
Support appropriate training, recruitment, and development requirements for matrix team resources

What we offer

Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
Discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models, including remote and hybrid work arrangements, where possible

Fulltime

New

Application Scientist, Clinical Genomics

Location

Spain

Salary:

Not provided

Saphetor

Expiration Date

Until further notice

Requirements

Master’s or PhD in Human Genetics, Laboratory Medicine, Molecular Biology/Pathology, Life Sciences, or related field
Hands-on experience in clinical genomics workflows, including NGS library preparation, sequencing, and secondary and/or tertiary analysis in a clinical setting
Solid grasp of variant classification frameworks and deep understanding of NGS workflows
Ability to simplify complex clinical genomics and bioinformatics concepts
Native in Spanish
Proficiency in English

Job Responsibility

Pre-sales Support: Act as the technical 'closer' by delivering expert demonstrations that bridge clinical needs with VarSome Premium and Clinical
own the customer evaluation process, solve 'pain points' around variant analysis, and advise on lab equipment/system integrations
Post-sales Support: Lead onboarding sessions for geneticists and bioinformaticians to ensure rapid 'time to value'
act as the primary lead for on-premises and private cloud deployments, coordinating infrastructure specifications between clients and our DevOps team
Workflow Optimization & Support: Fine-tune filtering strategies and automation to maximize platform 'stickiness' while acting as a high-level bridge between customer support and stakeholders
Scientific Advocacy: Systematically gather power-user feedback to influence the product roadmap and cultivate strategic relationships for conference presentations (ESHG, MedTech) and the development of technical white papers
Cross-functional Collaboration: Partner with Product, Marketing, and Operations to ensure product-market fit and growth

What we offer

Position in a fascinating healthcare growth domain, at the cutting edge of technology and research
A competitive compensation package tailored to your unique expertise and professional background
A remote-first work environment that promotes a healthy work-life balance
Endless learning opportunities, while transferring new technologies from academics to clinical practice all over the world

Fulltime

Director, Clinical Scientist

The Director, Clinical Scientist plays a key role in supporting the clinical dev...

Location

United States , Philadelphia

Salary:

Not provided

Cabaletta Bio Inc

Expiration Date

Until further notice

Requirements

Advanced degree (MS, Ph.D., Pharm.D., M.D., or equivalent) in a relevant scientific discipline preferred
4-5+ years of clinical development experience within biotech, pharmaceutical, or academic settings
Cell and gene therapy experience—particularly in CAR-T or T-cell–based modalities—strongly preferred
autoimmune disease experience highly desirable
Deep understanding of T-cell biology, immunology, and translational science principles relevant to cellular therapy
Proven ability to author and critically review clinical protocols, study reports, and regulatory documents
Demonstrated skill in analyzing complex clinical data, conducting literature reviews, and synthesizing insights to inform program strategy
Exceptional scientific judgment, attention to detail, and analytical rigor
Strong communication and collaboration skills
Highly organized with the ability to manage multiple priorities in a fast-paced, evolving environment.

Job Responsibility

Serve as a key clinical science contributor for assigned CAR-T programs, partnering with the Medical Director and other Clinical Development team members to support study design, execution, and interpretation across all phases of clinical development
Lead or contribute to the preparation of key clinical documents — including protocols, amendments, informed consent forms, investigator brochures, clinical study reports, and regulatory submissions (e.g., INDs, CTAs, DSURs, BLAs/MAAs)
Review, analyze, and interpret emerging clinical data (safety, efficacy, PK/PD) to identify trends and issues, ensuring timely resolution through cross-functional collaboration
Conduct literature and competitive landscape reviews to inform study design, data interpretation, and program strategy
Provide ongoing data review to ensure study conduct aligns with protocol, patient safety standards, and data integrity expectations
Collaborate with the Medical Monitor to ensure awareness of key safety and efficacy findings, supporting SAE review, narrative development, and safety governance activities
Lead or support governance activities, including preparation and presentation of materials for Development, Executive, and Scientific Steering Committees, as well as oversight of external boards (e.g., DSMB, adjudication committees)
Contribute to and present scientific and clinical data internally and externally (e.g., investigator meetings, scientific conferences, regulatory interactions)
Serve as the clinical science representative on cross-functional development and study teams, providing scientific and strategic input to ensure cohesive execution
Mentor study team members and contribute to vendor oversight to ensure consistency, quality, and scientific rigor across all clinical deliverables

What we offer

health and retirement
PTO
stock option plans

Fulltime

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