Clinical Site Manager II

Recruiter
PAREXEL
Location
South East England
Posted
13 Feb 2018
Closes
18 Feb 2018
Sector
Healthcare
Contract Type
Permanent
Hours
Full Time
PAREXEL strives to be the premier provider to the biopharmaceutical and medical device industries for the development and commercialization of new medical therapies worldwide. Our mission is to combine the strength of our expertise, experience and innovation to advance the worldwide success of the biopharmaceutical and medical device industries in preventing and curing disease. This role can be either home or office based from our UK Head Office situated in Uxbridge. This is close to both Uxbridge train station as well as the town centre and the building has plenty of free parking when you are not required to be on site.The Clinical Site Manager (CSM) is the clinical sites’ direct point of contact and accountable for managing site quality and delivery from site identification through close-out. The aim of this role is to build the relationship with the site, to be the sole position accountable for the site performance, including driving the site successfully to initiation, the development of a robust patient recruitment strategy, setting up of a system, assessing compliance with regulations and the site’s capability to comply with the study needs and recruitment expectations, and problem solving to address and resolve site issues.Your Key Accountabilities:Maintenance (from initiation through close out)Act as PAREXEL’s direct contact with assigned sites, assess and ensure overall integrity of study implementation and adherence to study protocol at clinical sites, and perform problem-solving to address and resolve site issues.- Build relationships with investigators and site staff.- Facilitate and support site with access to relevant study systems and ensure sites are compliant with project specific training requirements.- Evaluate if on-site staff assignment is still accurate and determine and implement corrective actions & follow-up, if necessary / relevant.- Actively participate in Investigator and other external or internal meetings and audits & regulatory inspections as required.- Collect, review, and approve (if applicable) updated/amended site documentation, including regulatory documents as applicable.- Evaluate site recruitment plan in collaboration with the site staff on an on-going basis and provide strategy for improvements.- Perform on-site visits; this includes Qualification and Initiation visits; apply judgment and knowledge to independently resolve site issues, questions and concerns.- Conduct remote visits/contacts as requested/needed.Overall Accountabilities from Site identification to Close out-Ensure timely and accurate completion of project goals and update of applicable trial management systems.- Work with team members to meet project goals, provide strategy for efficient project planning and goal completion, and encourage the support of team members where required.- Update all appropriate Clinical Trial Management Systems on an on-going basis, including performing regular reviews of site level data in clinical systems (e.g. CTMS, EDC, IVRS, and SIS) and ensure timely and high quality data entry compliance from sites, manage and submit all relevant documents to the Trial Master File (TMF).- Ensure that assigned sites are audit and inspection-ready.- Monitor and maintain compliance with ICH-GCP and applicable international and local regulations.QualificationsEducation:- Educated to degree level (biological science, pharmacy, or other health-related discipline preferred) or equivalent nursing qualification or other equivalent experience.Skills:- Sound problem solving skills.- Able to take initiative and work independently, and to proactively seek guidance when necessary.- Advance 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.- Willingness to work in a matrix environment and to value the importance of teamwork.- Strong computer skills including but not limited to the knowledge of a Clinical Trial Management System (CTMS), Electronic Document Management System (EDMS), and MS-Office products such as Excel and Word.- Consulting Skills- Able to accommodate travel time requirements, according to tasks allocation/phase of the study assigned.- Attention to detail.- Holds a driver’s licenseKnowledge and Experience:- Site Management experience or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology.- Strong previous onsite clinical monitoring experience is essential in the capacity of a CRA or equivalent performing all types of visits .In return we will be able to offer you a structured career pathway and development within the role including awareness and understanding of the industry. Your hard work will be rewarded with a competitive base salary, company car or car allowance plus a CSM incentive scheme as well as a benefits package including 25 days holiday per year, strong contributory pension scheme, life assurance, long term disability insurance, private medical and private dental cover as well as other leading edge benefits that you would expect with a company of this type.If you are ready to join PAREXEL’s Journey, please apply!

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