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Job Details

Clinical Trial Specialist

Company: DOCS Global
Location: Marlow,United Kingdom
Reference: Ref AS-016507
Closing Date: 11 Dec 16
Type: Contract
Salary (£): Competitive
Benefits: Excellent & Comprehensive

Job Summary:

Why Join DOCS? If you are an experienced clinical professional looking for an opportunity with a rapidly growing and fast paced global leader on an interesting and complex project this would be a compelling role for you. To express your interest please send your CV today to find out more details to Elisabeth.Knighton@docsglobal.com or ring +33 964 25 67 65. *Applicants who have not had a response within two weeks should assume their application has been unsuccessful.

Requirements:

Roles & Responsibilities of the position

We are looking for talented and motivated candidates to join the team and take part in this long term, dynamic project. The project will provide exposure across a variety of Therapeutic Areas with an organization that is on the forefront of adopting new processes and technologies, creating a unique opportunity for career growth and development.

Integral to the project is the role of an Associate Project Management.

Key Responsibilities include:
• Support the management and oversight of Global Clinical Trials
• Coordinate, author and manage preparation of clinical trial documentation
o Training Materials for CRAs/CTAs
o Investigator Meetings
o Site Evaluation and Initiation Training
o COV training
• Managing process for planning and procuring and oversight of ancillary clinical supplies
• Supporting global recruitment and retention initiatives
o Authoring global/country level recruitment plans
o Authoring global/country level retention plans
o Authoring and distribution of Study Newsletters
• Maintaining study level storyboard for critical timelines
• Facilitating authoring of Investigational Product Information Manual and study specific Important Protocol Deviation (IPD) list
• Vendor management
• Compiling IRB/EC submission documentation
• Assisting with Operational Review preparation
• Preparing Clinical Study Team meeting agendas and minutes
• Managing global versioning and distribution of informed consent forms (ICFs)
• Facilitating cross functional meetings
Critical Success Factors for the Role include:
• Indepth knowledge of drug development process
• Experience in or familiar with advanced concepts of clinical research
• Demonstrated success in a CRA or study management related role
• Extensive knowledge of technical, scientific and medical information
• Advanced computer skills
• Detailed knowledge of Good Clinical Practices (GCP), FDA regulations and guidelines, and applicable international regulatory requirements
• Ability to write and present clearly using scientific and clinical issues terminology
• Experience dealing with time demands, incomplete information or unexpected events
• Excellent communication skills
• Good organizational and planning skills
• Experience working effectively in a team/matrix environment
• Proactivity

Job Requirements

• BA/BS/BSc or RN
• Specialist experience working in life sciences or medically related field
• CRA experience preferable
• Previous biopharmaceutical clinical research experience obtained working on industry-sponsored or industry-partnered clinical trials, or working on clinical trials at a biotech, pharmaceutical or CRO company
• Full-time availability
• Full and valid UK working eligibility
• Ideally able to start asap/negotiable - must be able to start before May 2016

Key Competencies:
Proactivity / Attention to Detail / Teamwork / Strong Written and Oral Communication / Delivery Focus / Flexibility / Initiative / Relationship Building / Policy, Process and Procedural Conformance / Problem Solving / Time Management
What is offered
• Permanent contract of employment
• Full-time
• Office-based in Marlow
• Market leading salary ranging depending on level of skills and experience, plus company benefits (23 days annual leave, pension, healthcare cover, etc.)

Why Join DOCS?
If you are an experienced clinical professional looking for an opportunity with a rapidly growing and fast paced global leader on an interesting and complex project this would be a compelling role for you. To express your interest please send your CV today to find out more details to Elisabeth.Knighton@docsglobal.com or ring +33 964 25 67 65.

*Applicants who have not had a response within two weeks should assume their application has been unsuccessful.

Remuneration & other details

• Permanent contract of employment
• Full-time
• Office-based in Marlow
• Market leading salary ranging depending on level of skills and experience, plus company benefits (23 days annual leave, pension, healthcare cover, etc.)

Why Join DOCS?
If you are an experienced clinical professional looking for an opportunity with a rapidly growing and fast paced global leader on an interesting and complex project this would be a compelling role for you. To express your interest please send your CV today to find out more details to Elisabeth.Knighton@docsglobal.com or ring +33 964 25 67 65.

*Applicants who have not had a response within two weeks should assume their application has been unsuccessful.

Apply for this job: Clinical Trial Specialist

Contact Information:

Address:  DOCS UK
2 Globeside, Globeside Business park Marlow
SL7 1HZ
England
Reasons to work for Docs International
Tel:  +44 (0) 2380 688500
Fax:  +44 (0) 2380 688501
Website:  Visit Our Web Site

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