Manager, Scientific Affairs
About the role
This vacancy has now expired. Please click here to view live vacancies.
Manager, Scientific Affairs
Home Based
The Manager, Scientific Affairs plays a role in establishing and maintaining partnerships with pharmaceutical and biotech clinical drug development programs. As such, this individual will participate in customer facing meetings to provide technical and scientific support to ascertain customer needs for assay development, validation, clinical trial testing and CDx strategy as needed.
Responsibilities
- Provide scientific support for client oriented business development and related contractual activities as a subject matter expert on related technologies and methods for oncology biomarker analysis and clinical diagnostics.
- Act as technical writer and editor for development project and clinical trial proposal documents
- Act as a technical writer and editor for product marketing collateral * Define and assess current oncology drug classes, biomarkers and technology platforms. Evaluate oncology diagnostic assay market trends and opportunities for strategic planning purposes
- Perform competitor analysis; provide updates on products and services offered by commercial laboratories who operate in oncology biomarker assay development, clinical trial testing and companion diagnostics development
- Act as liaison between internal business development and assay development teams on a project specific basis
- Partner to implement the strategic product development plan and in the development and of product requirements for proposed new products and services. Involves close interaction with development leads, product development teams, and key customers.
- Provide support for IP assessment
- Participate in company presentations to clients
- Develop and edit scientific content for marketing material and project proposals
- Evaluate potential strategic partners and markets with respect to platforms, chemistries, biomarkers and applications
- Manage database to track oncology drug pipelines, trials and associated biomarkers
- Maintain knowledge of related industry news and trends
- Identify new opportunities to collaborate in clinical biomarker studies with both industry and academic partners
- Analyze the competitive landscape for and current and potential new product/services
- Maintain the product portfolio roadmap
- Define user/client personas for individual products and services
- Write product requirements and user scenarios
Requirements
- At least 8 years' experience in a related position/field
- Bachelors degree required, Masters plus preferred
Benefits of Working in ICON
ICON enjoys a strong reputation for quality and is focused on staff development. We make it our mission to attract the most diverse and creative minds into the business and we continually strive to provide opportunities for our people to excel, grow and build a great career. We understand that our greatest asset is the skills and talents of our people and they are truly what set us apart.
Other than working with a great team of smart and energetic people, we also offer a very competitive benefits package. This varies from country to country so a dedicated recruiter will discuss this with you at interview stage.
We care about our people as they are the key to our success. We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term career.
ICON is an equal opportunity employer - M/F/D/V and committed to providing a workplace free of any discrimination or harassment
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. See all locations Learn more about Our Culture at ICON
Day in the life
.png)
Teaser label
Inside ICONContent type
BlogsPublish date
05/08/2025
Summary
Standing Strong on Ovarian Cancer Day: ICON's Commitment to Advancing Care Ovarian cancer remains one of the most challenging gynaecologic malignancies, both in terms of detection and treatmen
.png)
Teaser label
IndustryContent type
BlogsPublish date
05/07/2025
Summary
Patient Centricity in Clinical Research: What it is and Why it Matters In the past, clinical research was designed around the needs of sponsors, researchers, and regulatory bodies. Patients were of
.png)
Teaser label
IndustryContent type
BlogsPublish date
05/05/2025
Summary
Navigating Regulatory Landscapes: Comparing FDA, EMA, & MHRA in Clinical Trials In clinical research, no matter how promising a new therapy may be, it will go nowhere without regulatory appro
Similar jobs at ICON
Salary
Location
Taipei
Department
Clinical Monitoring
Location
Taipei
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a CRAII or Senior CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.Working location: Taiwan Homebased
Reference
2025-119586
Expiry date
01/01/0001
Author
Sandy TangAuthor
Sandy TangSalary
Location
France
Department
Clinical Monitoring
Location
France
Remote Working
Office Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own I
Reference
2025-119535
Expiry date
01/01/0001
Author
Dominique CarilienAuthor
Dominique CarilienSalary
Location
Mexico
Department
Clinical Operations Roles
Location
Mexico
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
As a Senior TMF Lead you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. You will be joining one of our global pharmaceutic
Reference
2025-119114
Expiry date
01/01/0001
Author
Magda ObregonAuthor
Magda ObregonSalary
Location
France
Department
Clinical Trial Management
Location
France
Remote Working
Office Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotech
Reference
2025-119601
Expiry date
01/01/0001
Author
Dominique CarilienAuthor
Dominique CarilienSalary
Location
Canada
Department
Clinical Operations Roles
Location
Canada
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Contracts Administration
Job Type
Permanent
Description
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us
Reference
2025-119596
Expiry date
01/01/0001
Author
Jonathan HolmesAuthor
Jonathan HolmesSalary
Location
United States, Canada
Department
Clinical Operations Roles
Location
Canada
United States
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
As a CLinical Quality Compliance Lead you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Reference
2025-119563
Expiry date
01/01/0001
Author
Melissa BennerAuthor
Melissa Benner