About this role
TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service capabilities resourcing and Functional Service (FSP) solutions.
Currently we are looking for a Study Start Up Manager for a direct recruitment for one of our clients a Big Pharma company.
Please keep in mind that this is a hybrid position with 3 days per week at the clients office in Hamburg or Munich.
Key Responsibilities
Manage and execute study start-up activities at country and site level in compliance with ICH-GCP and applicable regulations
Prepare review track and submit regulatory and ethics documentation to authorities and IEC/IRBs
Maintain and report on site performance metrics and start-up milestones
Collaborate closely with CRAs and the local study team to ensure efficient study start-up delivery
Update CTMS and other systems in line with required timelines
Ensure timely collection and quality of essential documents in the eTMF
Follow up with sites to resolve outstanding start-up actions
Participate in local study team meetings and provide regular status updates to line management
Qualifications:
Bachelors degree in life sciences or a related field
Strong knowledge of ICH-GCP and local regulatory requirements
Solid understanding of clinical study management and start-up processes
Experience with EU and local/site submission processes
Strong communication collaboration and organizational skills
High attention to detail and ability to manage multiple priorities
Cell therapy experience
Ability to work 3 days per week from the office in Hamburg / Munich
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 Sweden in the city of Lund. As a full-service global Contract Research Organization (CRO) 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 are our guiding light serving as the framework for decision-making at all levels of the organization. They assist us in attracting and retaining valuable talent who share our sentiments resulting in high employee engagement and satisfaction. By aligning on these fundamental values we cultivate a unified force geared towards innovation and excellence. This collective effort propels us towards our shared goal and fosters a culture of mutual respect and collaboration. Together we 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 entire clinical development journey. Our expertise includes full service capabilities resourcing and Functional Service (F...
About this role
TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service capabilities resourcing and Functional Service (FSP) solutions.
Currently we are looking for a Study Start Up Manager for a direct recruitment for one of our clients a Big Pharma company.
Please keep in mind that this is a hybrid position with 3 days per week at the clients office in Hamburg or Munich.
Key Responsibilities
Manage and execute study start-up activities at country and site level in compliance with ICH-GCP and applicable regulations
Prepare review track and submit regulatory and ethics documentation to authorities and IEC/IRBs
Maintain and report on site performance metrics and start-up milestones
Collaborate closely with CRAs and the local study team to ensure efficient study start-up delivery
Update CTMS and other systems in line with required timelines
Ensure timely collection and quality of essential documents in the eTMF
Follow up with sites to resolve outstanding start-up actions
Participate in local study team meetings and provide regular status updates to line management
Qualifications:
Bachelors degree in life sciences or a related field
Strong knowledge of ICH-GCP and local regulatory requirements
Solid understanding of clinical study management and start-up processes
Experience with EU and local/site submission processes
Strong communication collaboration and organizational skills
High attention to detail and ability to manage multiple priorities
Cell therapy experience
Ability to work 3 days per week from the office in Hamburg / Munich
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 Sweden in the city of Lund. As a full-service global Contract Research Organization (CRO) 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 are our guiding light serving as the framework for decision-making at all levels of the organization. They assist us in attracting and retaining valuable talent who share our sentiments resulting in high employee engagement and satisfaction. By aligning on these fundamental values we cultivate a unified force geared towards innovation and excellence. This collective effort propels us towards our shared goal and fosters a culture of mutual respect and collaboration. Together we make a difference.
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