Job Title: Senior Clinical Research Associate.
Location: Uxbridge, London.
Position Type: Permanent.
As a Senior Clinical Research Associate you will be the direct point of contact for the clinical sites and will manage site quality and delivery from site identification through close out. You will be responsible for building the relationship with the site. Solely responsible for the sites performance, developing a robust patient recruitment strategy, problem solving to address and resolve site issues. You will also assess compliance with regulations and the sites capability to comply with the study needs and recruitment expectations.
Acting as the companys direct point of contact for the assigned sites.
Building relationships with site staff and investigators.
Facilitate and support staff with access to relevant study systems.
Evaluate and implement corrective actions to ensure on site staff assignments are still accurate.
Working with team members to meet project goals.
Continuously updating Clinical Trial Management Systems (CTMS), including performing regular reviews.
Ensuring all sites are audit and inspection ready.
Monitor and maintain compliance with applicable international and local regulations.
Delegating administrative and other tasks to Administrative Support Team.
All above duties, including other duties to fulfil the clients needs as and when needed.
Strong problem-solving skills.
Able to take initiative and work independently, and to proactively seek guidance when necessary.
Excellent presentation skills.
Client focused approach to work.
Ability to interact professionally within a client organization.
Flexible attitude with respect to work assignments and new learning.
Ability to prioritize multiple tasks and achieve project timelines; utilizing strong analytical skills to make decision autonomously due to the unpredictable nature of the issues that arise.
Strong ability to make appropriate decisions in ambiguous situations.
Willingness to work in a matrix environment and to value the importance of teamwork.
Shows commitment to and performs consistently high-quality work.
Knowledge and Experience:
Substantial Site Management experience or equivalent Senior CRA or advanced level onsite monitoring experience in clinical research with understanding of clinical trials methodology and terminology
Very strong and advanced previous onsite clinical monitoring experience is essential in the capacity of a Sr CRA or equivalent performing all types of visits.
You will receive a structured career path, competitive base salary, car allowance or company car. A benefits package, 25 days holiday per year and strong contributory pension scheme, life assurance, long term disability insurance. You will also receive private dental and medical care as well as many other benefits.
If this role is something you would be interested in please email your CV to Joshua.firstname.lastname@example.org or call Josh on 0118 959 4990.
Clinical Professionals is the leading pharmaceutical staffing consultancy in Europe. Our dedicated Clinical Team has over 10 years experience placing professionals into positions within Pharmaceutical, Biotech, CRO, Charity, and Academia organisations. We work with global market leaders as well as partnering SMEs and start-ups.
- Agency: Clinical Professionals
- Contact: Josh Wicks
- Reference: JO-1903-426523
- Posted: 15th March 2019
- Expires: 12th April 2019