About this role
TFS HealthScience is a leading global mid size Contract Research Organization that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service capabilities resourcing and Functional Service solutions.
The Clinical Scientist is responsible for providing scientific support to clinical development programs contributing to the planning execution and interpretation of clinical studies while ensuring scientific quality and regulatory compliance.
As part of our SRS FSP team you will be dedicated to one sponsor a global pharmaceutical or biotechnology company recognized for its innovation and commitment to advancing patient care.
Approximately: 0.5 FTE
Key Responsibilities
Contribute to the scientific design and implementation of clinical studies including protocol development and study documentation
Provide scientific input throughout study start up conduct and closeout to ensure data quality and adherence to protocol
Review and interpret clinical data to identify trends potential risks and scientific insights
Collaborate with cross functional teams including clinical operations biostatistics data management regulatory and medical teams
Support preparation of clinical and regulatory documents reports and presentations
Ensure compliance with applicable regulations guidelines and internal procedures
Qualifications
Advanced scientific degree in life sciences biomedical sciences or a related field
Experience working in clinical development or clinical research within the pharmaceutical biotech or CRO environment
Solid knowledge of clinical trial methodology and GCP principles
Ability to analyze and interpret complex clinical data
Strong written and verbal communication skills
Ability to work effectively in a collaborative and fast paced environment
What We Offer
We provide a competitive compensation package comprehensive benefits and the opportunity for personal and professional growth in a rewarding environment. You will be joining a team that values collaboration innovation and making a difference in the lives of patients.
A Bit More About Us
Our journey began over 27 years ago in Sweden in the city of Lund. As a full service global Contract Research Organization we build solution driven teams working towards a healthier future. Bringing together over 800 professionals TFS delivers tailored clinical research services in more than 40 countries with flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology Neuroscience Oncology and Ophthalmology.
Our core values of Trust Quality Passion Flexibility and Sustainability guide decision making at all levels of the organization. They help us attract and retain talented professionals who share our values and foster a culture of collaboration innovation and mutual respect. Together we make a difference.
About this roleTFS HealthScience is a leading global mid size Contract Research Organization that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service capabilities resourcing and Functional Service solution...
About this role
TFS HealthScience is a leading global mid size Contract Research Organization that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service capabilities resourcing and Functional Service solutions.
The Clinical Scientist is responsible for providing scientific support to clinical development programs contributing to the planning execution and interpretation of clinical studies while ensuring scientific quality and regulatory compliance.
As part of our SRS FSP team you will be dedicated to one sponsor a global pharmaceutical or biotechnology company recognized for its innovation and commitment to advancing patient care.
Approximately: 0.5 FTE
Key Responsibilities
Contribute to the scientific design and implementation of clinical studies including protocol development and study documentation
Provide scientific input throughout study start up conduct and closeout to ensure data quality and adherence to protocol
Review and interpret clinical data to identify trends potential risks and scientific insights
Collaborate with cross functional teams including clinical operations biostatistics data management regulatory and medical teams
Support preparation of clinical and regulatory documents reports and presentations
Ensure compliance with applicable regulations guidelines and internal procedures
Qualifications
Advanced scientific degree in life sciences biomedical sciences or a related field
Experience working in clinical development or clinical research within the pharmaceutical biotech or CRO environment
Solid knowledge of clinical trial methodology and GCP principles
Ability to analyze and interpret complex clinical data
Strong written and verbal communication skills
Ability to work effectively in a collaborative and fast paced environment
What We Offer
We provide a competitive compensation package comprehensive benefits and the opportunity for personal and professional growth in a rewarding environment. You will be joining a team that values collaboration innovation and making a difference in the lives of patients.
A Bit More About Us
Our journey began over 27 years ago in Sweden in the city of Lund. As a full service global Contract Research Organization we build solution driven teams working towards a healthier future. Bringing together over 800 professionals TFS delivers tailored clinical research services in more than 40 countries with flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology Neuroscience Oncology and Ophthalmology.
Our core values of Trust Quality Passion Flexibility and Sustainability guide decision making at all levels of the organization. They help us attract and retain talented professionals who share our values and foster a culture of collaboration innovation and mutual respect. Together we make a difference.
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