Study Startup Specialist II

PSI CRO AG; Oxford; On-site; GBP 30,000 - 50,000; Full time

Job summary

A leading global clinical research organization seeks a Study Startup Specialist II in Oxford to support clinical research teams. You will ensure smooth project initiation, manage documentation, and meet tight timelines in a collaborative environment. Ideal candidates will have a Life Sciences degree and relevant experience in Clinical Trials, alongside excellent communication skills.

Benefits

Excellent working conditions

Extensive training

Competitive salary and benefits package

Opportunities for personal and professional growth

Qualifications

• Preferably 2 years of Clinical Trial experience in the UK.
• Study Startup experience would be an advantage.

Responsibilities

• Collaborate with project team for site activation processes.
• Collect site documents for IRB/IEC submission.
• Meet site activation targets through startup timelines.

Skills

Communication

Organizational skills

Education

College/University degree in Life Sciences

Job description

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,800 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then PSI is the right choice for you.

Job Description

As as Study Startup Specialist II, you will support clinical research teams and ensure PSI projects start smoothly and on time.

You will:

• Collaborate with the project team for site activation processes
• Collect site documents for IRB/IEC submission and/or IP-RED process
• Identify and escalate project-specific issues as needed
• Prepareand submitthe study dossiers to sites, competent authorities, IRBs/IECs
• Ensureexchange of information and documentation with investigational sites andoff site facilities
• Participatein development of site-specific startup timelinesand is responsible for meeting the site activation targets

Qualifications

• College/University degree in Life Sciences or an equivalent combination of education, training and experience
• Preferably 2 years of Clinical Trialexperience in the UK (Study Startup experience would be an advantage)
• Well-developed communication and organizational skills

Additional Information

We offer:

• Excellent working conditions
• Extensive training and friendly team
• Competitive salary and benefits package
• Opportunities for personal and professional growth

Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.