Life Science Professionals – Denmark

Copenhagen - Denmark

Monthly Salary: Not Disclosed

Posted on: 30+ days ago

Vacancies: 1 Vacancy

Job Summary

About this role

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their clinical development journey. Our expertise includes full-service capabilities resourcing and Functional Service (FSP) solutions.

We are always looking to connect with talented life science professionals interested in exploring opportunities with TFS HealthScience. Whether your expertise is in preclinical research clinical development or post-market activities we invite you to join our network and be considered for exciting projects across our global CRO operations.

As part of our SRS/FSP team you will be dedicated to supporting one or more sponsor projects collaborating with global pharmaceutical or biotech companies to drive high-quality outcomes.

Key Responsibilities

Contribute to projects across clinical trials safety regulatory or other life science functions.
Collaborate with internal teams and sponsor representatives to deliver project objectives.
Ensure adherence to quality standards regulatory guidelines and project timelines.
Support documentation reporting and analysis relevant to your area of expertise.
Participate in continuous improvement initiatives and knowledge sharing.

Qualifications

Experience in the life sciences industry (e.g. clinical trials pharmacovigilance regulatory or related fields).
Strong communication and collaboration skills.
Ability to manage multiple tasks and priorities in a fast-paced environment.
Attention to detail and commitment to quality.
Adaptability and eagerness to learn new skills and take on diverse challenges.

What We Offer
We provide a competitive compensation package comprehensive benefits and the opportunity for personal and professional growth in a rewarding environment. Youll 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 Lund Sweden. As a full-service global CRO TFS brings together over 800 professionals to deliver tailored clinical research services in more than 40 countries. We provide 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 our decisions at every level. These values help us attract and retain talent foster high engagement and create a collaborative culture where everyone can make a difference.

About this roleTFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their clinical development journey. Our expertise includes full-service capabilities resourcing and Functional Service (FSP) sol...

About this role

As part of our SRS/FSP team you will be dedicated to supporting one or more sponsor projects collaborating with global pharmaceutical or biotech companies to drive high-quality outcomes.

Key Responsibilities

Contribute to projects across clinical trials safety regulatory or other life science functions.
Collaborate with internal teams and sponsor representatives to deliver project objectives.
Ensure adherence to quality standards regulatory guidelines and project timelines.
Support documentation reporting and analysis relevant to your area of expertise.
Participate in continuous improvement initiatives and knowledge sharing.

Qualifications

Experience in the life sciences industry (e.g. clinical trials pharmacovigilance regulatory or related fields).
Strong communication and collaboration skills.
Ability to manage multiple tasks and priorities in a fast-paced environment.
Attention to detail and commitment to quality.
Adaptability and eagerness to learn new skills and take on diverse challenges.