Clinical Scientist Job at Unilever (Trumbull)

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

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

Location

United Kingdom , Northampton

Salary:

43000.00 GBP / Year

CARE Fertility

Expiration Date

Until further notice

Requirements

HCPC registered
ICSI-trained Clinical Embryologist
Biopsy training is an advantage but not essential
Professionalism, curiosity, and compassion

Job Responsibility

Play a vital role in all aspects of laboratory work, including oocyte collection, sperm preparation and freezing, insemination and ICSI, fertilisation and embryo assessment, embryo freezing and transfer, and oocyte cryopreservation
Weekend and bank holiday cover on a rota basis

What we offer

33 days’ annual leave (inc. public holidays)
Pension scheme
Life assurance
Retail discounts
Wellbeing hub
Holiday trading
Internal training programmes
Funded external courses
A clear path for career progression
Access to Caremaps-Ai (award-winning embryo selection technology)

Fulltime

Clinical Scientist Director - Late Development Oncology

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

Location

Portugal , Lisbon

Salary:

105822.45 - 143171.55 EUR / Year

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree and 4 years of life sciences/healthcare experience
Master’s degree and 7 years of life sciences/healthcare experience
Bachelor’s degree and 9 years of life sciences/healthcare experience

Job Responsibility

Serve as a clinical and scientific subject-matter expert for the assigned therapeutic area and disease indication, with a strong focus on protocol execution and data integrity
Contribute to medical monitoring activities and support ongoing assessment of subject-level clinical data to identify trends, risks, and emerging issues
Present information internally and externally, anticipating and actively managing problems across a broad spectrum of cross-functional teams
Provide guidance and assistance in the identification and management of collaborators, consultants, and/or Clinical Research Organizations (CROs) in completion of key projects
Work cross functionally to ensure clinical strategy is translated into the development of the study concept document, study protocol, and related documents
Ensure integrity of protocols and/or components of clinical plans and for the delivery of final protocol and its governance approval
Provide clinical input into & implementation of clinical trial(s), delivery, clinical data review, and interpretation of results
Review and analyze clinical trial data to ensure accuracy, completeness, and adherence to protocol and regulatory requirements
Conduct thorough data quality assessments in the context of a data monitoring plan to maintain high standards of data accuracy and integrity throughout the trial lifecycle

What we offer

health and welfare plans for staff and eligible dependents
financial plans with opportunities to save towards retirement or other goals
work/life balance
career development opportunities
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
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models including remote and hybrid work arrangements where possible

Fulltime

New

Clinical Scientist Director - Late Development Oncology

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

Location

Portugal , Lisbon

Salary:

105822.45 - 143171.55 EUR / Year

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree and 4 years of life sciences/healthcare experience OR Master's degree and 7 years of life sciences/healthcare experience OR Bachelor's degree and 9 years of life sciences/healthcare experience

Job Responsibility

Serve as a clinical and scientific subject-matter expert for the assigned therapeutic area and disease indication, with a strong focus on protocol execution and data integrity
Contribute to medical monitoring activities and support ongoing assessment of subject-level clinical data to identify trends, risks, and emerging issues
Present information internally and externally, anticipating and actively managing problems across a broad spectrum of cross-functional teams
Provide guidance and assistance in the identification and management of collaborators, consultants, and/or Clinical Research Organizations (CROs) in completion of key projects
Work cross functionally to ensure clinical strategy is translated into the development of the study concept document, study protocol, and related documents
Ensure integrity of protocols and/or components of clinical plans and for the delivery of final protocol and its governance approval
Provide clinical input into & implementation of clinical trial(s), delivery, clinical data review, and interpretation of results
Review and analyze clinical trial data to ensure accuracy, completeness, and adherence to protocol and regulatory requirements
Conduct thorough data quality assessments in the context of a data monitoring plan to maintain high standards of data accuracy and integrity throughout the trial lifecycle

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
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models, including remote and hybrid work arrangements, where possible

Fulltime

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

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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