Ref #: 29765

Employment type: Permanent - Full-Time

Location: Eastleigh Southampton Hampshire / England

Posted: 07-Jun-2021


Some of your responsibilities will include:
• Supporting the management and oversight of global clinical trials
• Essential document management
• Compiling IRB/EC submission documentation
• To coordinate, author and manage preparation of clinical trial documentation and training materials
• Facilitate development of Investigational Product Information Manual and study specific Important Protocol Deviation list
o Global/country level recruitment and retention materials
o Authoring and distribution of study newsletters
• Vendor management (including set up, tracking and issue resolution over the life of the study)
• Preparing clinical study team meeting agendas and minutes, facilitating cross-functional meetings

What is required
• Ideally a minimum of 2/3 years’ experience gained within the clinical research industry on commercial clinical studies within a CRO, pharmaceutical or biotech working environment
• CRA/clinical trial monitoring experience would be preferred
• Proactive, flexible and problem-solving work approach with strong policy, process and procedural conformance
• BA/BS/BSc in life sciences or RN
• Full and valid UK working eligibility

What is offered
• Permanent full time contract of employment with DOCS seconded to the client
• Structured 4-week training for all new starters
• Office-based near Southampton/Hampshire (UK) 3 days per week with 2 days home-working per week.
• Salary depending on level of skills and experience plus company benefits (23 days annual leave, pension, healthcare cover, etc.)

For more detail, contact me at to or ring +33 964 25 67 65.