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	If you would like to post a job advertisement here, please contact webmaster Diabetes Research Nurse - posted on 01 September 2008 Centre for Clinical Research and effective practice (CCRep) is an organisation that is going places and wants you along to enjoy the ride……… We have an exciting new opportunity for an experienced research nurse to manage new trials in Diabetes research: CCRep operates like no other research team in NZ? With……………… Fantastic support, which is located literally right next door Professional development programs in Research Mentorship throughout your initiation period and beyond A dynamic team environment No shift work – flexible hours The chance of International travel to Investigator meetings A competitive salary package and re-location package (if outside of Auckland region) A great Health & Wellness programme for all employees We are looking for………………… Someone with an enquiring mind and a passion for Clinical Research Able to communicate to people of widely different backgrounds and cultures A self starter who can organise their day and manage their own time Good presentation skills Previous experience in Diabetes an advantage (not essential) Registered nurse with current annual practicing certificate We invite you to be part of this effective practise Apply ONLINE today www.aucklandhealthcareers.co.nz or for informal enquiries please contact Mary Baldwin on (09) 276 0044, ext 2949 For further information visit our website www.ccrep.org.nz Closing Date: 15th September 2008 Clinical Project Manager - posted on 27 August 2008 Clinical Trials Research Unit Customer focus Full-time position for 12 months Travel required within New Zealand The Clinical Trials Research Unit is located within the School of Population Health at The University of Auckland Tamaki campus. The Unit is focussed on innovative research aiming to reduce the major risks to health. An opportunity is available for an experienced Project Manager to co-ordinate a new Phase II trial of a therapy for the treatment of leg ulcers. This is a community-based trial with recruitment of participants planned in Auckland, Hamilton and Christchurch. The key responsibilities include management of the trial from set-up to close out, monitoring achievement of recruitment goals, site visits, and assuring adherence to Good Clinical Practices, Standard Operating Procedures and study protocols. Requirements The successful candidate will have previous experience in clinical project management and knowledge of GCP, the ability to multi-task and good team leadership skills. You will need to be confident, outgoing and have excellent communication skills as the job requires liaison with health providers within the community. This is a full-time position for 12 months and is based in Auckland. Previous experience in community nursing and/or clinical trial management would be an advantage. A vehicle and current driver’s licence are also essential for this role. Please apply by sending your CV and covering letter, by 8 September 2008 to: jobs@ctru.auckland.ac.nz. For further information please see www.ctru.auckland.ac.nz or contact the Operations Manager on the above email address. For a copy of the Job Description klick here. Clinical Database administrator (Fixed-Term) - posted on 12 August 2008 Cardioendocrine Research Group - Department of Medicine - Christchurch School of Medicine & Health Sciences This is full time, 15 month fixed term position. The selected candidate will be responsible for the design and maintenance of clinical databases, perform data audits and analysis, provide technical support and assist in the final transfer of datasets for statistical analysis. This person will be expected to develop and maintain project-specific databases for the entry of clinical data, load data into the clinical databases, format and transfer databases for statistical analysis according to study requirements, attend project meetings and communicate with investigators and study coordinators, create and maintain study documentation in accordance with Standard Operating Procedures (SOPs), assist and guide new personnel, supervise quality reviews of databases to ensure problems are documented and resolved, suggest improvements based on quality reviews, act as client interface for all database and programming issues, assist in management of database resources to ensure project objectives are met, review and implement strategies to increase quality and efficiency of the team and identify training needs and training courses required to develop the team and individuals. Requirements . The candidate will possess a university degree or have equivalent qualifications and experience in PC based MS Access and Excel applications. Excellent oral and written communication skills, and experience or equivalent in Database Administration are required. Previous experience in a hospital or health service environment would be an advantage. You will have the opportunity to work with a world leading clinical research team in a stimulating environment. University conditions of employment apply, including a 37.5 hour (Monday to Friday) working week. A competitive salary will be offered to the right candidate. For further information including application forms, please contact Rowena Fisher Please address your application to Rowena Fisher, University of Otago. Department of Medicine, Christchurch School of Medicine and Health Sciences, PO Box 4345, Christchurch. CRA/SCRA - Auckland based - posted on 07 July 2008 Are you in Auckland and looking for a new and interesting CRA role? This is a progressive company who care for it's staff! Auckland based role Work from home You know the New Zealand market is small and that opportunities that will really help you realise your potential are few and far between. That's why you should pick up your phone right now and dial my number! +61 2 8081 4308. My client is a progressive, medium sized business that puts it's people at it's core. You will be looked after as part of the family and will be working on interesting therapeutic areas. If this sounds like the next step for you, all you have to do is tick the below criteria and apply! Minimum of 12 months monitoring experience Passion and enthusiasm for Clinical Research Degree in a life science related field Good understanding of ICH/GCP guidelines Don't wait as this opportunity could well be snapped up quickly! Call Margaret on +61 2 8081 4308 or email your CV to me at margaret@hahnhealthcare.com.au An attractive and generous salary package will be offered to the right candidate Clinical Research Associate - posted on 03 July 2008 Home Office Based - New Zealand At Covance, you can make a difference by helping to deliver life-saving and life-enhancing medicines to people around the world. Our commitment to this mission has resulted in Covance’s impressive history of company stability and growth. We’ve achieved these results by fostering a work environment that encourages, develops and leverages our team’s capabilities. Covance’s ongoing success offers team members unsurpassed growth and career development opportunities. There is no better time to join us! Job Summary: May manage small projects under direction of a Project Manager/Director. May serve as lead monitor for a protocol or project & assist in establishing monitoring plans. Review progress of projects & initiate appropriate actions to achieve target objectives. Organize/make presentations at Investigator Meetings. Report, write narratives and follow-up on serious adverse experiences. Interact with internal work groups to evaluate needs, resources and timelines. Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties as assigned. General On-Site Monitoring Responsibilities Ensure that study staff have received the proper materials and instructions. Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements. Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document review. Monitor data for missing or implausible data. Ensure the resources of the Sponsor and Covance are spent wisely by performing the required monitoring tasks in an efficient manner, according to SOPs and established guidelines. Prepare accurate and timely trip reports. Experience: Minimum of two years of clinical research monitoring experience (including pre-study, initiation, routine monitoring and closeout visits). In lieu of the above requirements, candidates with three years of site management and/or registry administration experience will be considered. Ability to monitor study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines. Have a full understanding of the Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs. Good planning, organization and problem solving abilities. Ability to work with minimal supervision. Good communication, interpersonal, analytical and negotiation skills. Computer competency. Fluent in local office language and in English, both written and verbal. Works efficiently and effectively in a matrix environment Qualifications: University/college degree (life science preferred), or certification in a related allied health profession from an accredited institution (e.g., nursing certification, medical or laboratory technology). In lieu of the above requirement, candidates with three or more years of relevant clinical research experience will be considered Thorough knowledge of ICH Guidelines and GCP including a basic understanding of regulatory requirements. Thorough knowledge of monitoring procedures. Basic understanding of the clinical trial process. At Covance, we help make the miracles of medicine a reality. We offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career. To apply for this exciting opportunity, please forward your CV to Kenneth.Schneider@workplacegroup.com . Covance is committed to diversity in the workplace and is an equal opportunity employer. (M/F/D/V). Your confidentiality and privacy are important to us There are currently no further open positions posted.