Parexel International P

Senior Clinical Research Associate (BB-4A83D)

Encontrado en: Buscojobs

Voice the ideas that get treatments to patients faster br br Promoted to Senior Director of Clinical Application Development and Technology br br Naresh Senior Director of Clinical Application Development and Technology br br Keyword br br Location br br Senior Clinical Research Associate br br Colombia Any Region Home Based Date posted 12 04 2020 Job ID 64778BR br br Everything we do has the potential to impact patient lives and our Clinical Research Associates CRAs take their work seriously demonstrate empathy and act with heart They also perform with urgency navigating our streamlined clinical operating model to drive effectiveness reduce handoffs and increase employee client and site satisfaction br br As a CRA at Parexel you ll be joining a team with a wide variety of experiences and knowledge We re looking for people like you to take the initiative to do things better and smarter people who want to grow personally and professionally We recognize and uphold the importance of all people the way we do things our quest for innovation and most importantly our patients br br Check out the top traits we re looking for and see if you have the right mix br br Problem Solver br Tech Savvy br Confident br br The last 4 5 years I had a steep learning curve and I am still learning via on the job challenges and solid management feedback Next to my personal growth I also enjoy our open atmosphere and the great collegiality br br Rewards br br Global Impact br br We are one truly global team working together to propel each client s journey ahead faster br br Balance br br We value work life balance We try and keep regular hours and an emphasis on life outside the office br br Work with industry leaders and subject matter experts br br Freedom br br The ability to innovate ask what if and try new solutions without fear of failure br br Variety br br Opportunities to work on multiple accounts never boring br br Compensation br br Competitive salaries and bonus structure based on individual metrics br br Responsibilities br br Your time here br br At Parexel the CRA role offers the opportunity to go beyond the role of a typical clinical monitor CRA s are accountable for using their expertise to build and maintain the site relationship and ensure they re set up for success As the clinical sites sole point of contact this includes addressing and resolving site issues and questions You ll also manage site quality and delivery from site identification through to close out br br As a CRA Parexel will offer you world class technology and training catered to your individual experience You can anticipate less travel and a lower protocol load in comparison to industry peers Your hard work may be rewarded through a bonus incentive program the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical research If impact flexibility and career development appeal to you Parexel could be your next home br br What you ll do br br Leverage your expertise Conduct qualification visits QV site initiation visits SIV monitoring visits MV and termination visits TV at assigned clinical sites and generate visit contact reports br Build relationships Oversee integrity of the study and utilize problem solving skills to promote rapport with the site and staff br Protect patients Review the performance of the trial at designated sites ensure the rights and well being of human subjects are safeguarded and are in accordance with protocol br Drive productivity Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines while also ensuring compliance with the approved standard operating procedures SOPs protocol amendment s GCP and the applicable regulatory requirement s br Ensure quality Evaluate the quality and integrity of the reported data site efficacy and drug accountability br Execute Monitor the completeness and quality of Regulatory Documentation and perform site document verification br br More about you br br On your first day we ll expect you to have br br Substantial Site Management experience or equivalent experience in clinical research with understanding of clinical trials methodology and terminology br The ability to function as a mentor and role model for other CRAs br Bachelor s or equivalent degree in biological science pharmacy or other health related discipline br Strong interpersonal written and verbal communication skills within a matrixed team br Experience working in a self driven capacity with a sense of urgency and limited oversight A client focused approach to work and flexible attitude with respect to assignments new learning br The ability to manage multiple tasks evaluate a variety of unpredictable scenarios and achieve project timelines while being able to apply your understanding of study protocol s br An honest and ethical work approach to promote the development of life changing treatments for patients br 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 br br A little about us br br Parexel is proud to be a leading Clinical Research Organization with colleagues across the globe As a member of our team you ll get to know your coworkers on a personal level Have a question A clinical research leader project team member technology super user or collaborator are a phone call away Our clinical research teams meet regularly to have discussions in an open environment allowing our team members to share their expertise and promote learning within the team Management supports and encourages career growth through consistent performance discussions and evaluations Whether your interest is to progress into a more senior level CRA role into line management Quality Project Leadership or a variety of other positions Parexel prides itself on career opportunities for our employees br br Get the latest Parexel career opportunities as soon as they become available

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