Central monitoring associate - sponsor dedicated - (21006458) description
Central monitoring associate i - sponsor dedicated
Sponsor dedicated - home based
Come discover what our 25,000+ employees already know: work here matters everywhereWe’re a growing and evolving biopharmaceutical industry leader, which means you’ll have endless opportunities to work with experts around the world and build the career you’ve dreamed of. As a part of the syneos health team, you’ll help us deliver results for a rewarding reason – we improve patients’ lives around the worldBecause to us, a patient isn’t just a number, they’re our family, friends, and neighbors.
Why syneos health
#syneoshealthlife means we’re committed to our total self culture – where everyone can authentically be themselvesOur total self culture is what unites us globally, and we know every person’s unique contributions make a difference. We believe our success is a direct result of the people who are driving it – you! we value your dedication to care for our customers and patients, so we want to focus on taking care of youThat’s why we offer a comprehensive benefits program encompassing your total health - physical, mental and financial. We are continuously building the company we all want to work for and our customers want to work withWhy? because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong.
Performs remote site qualification, site initiation, site monitoring calls, and close-out visits ensuring regulatory, ich-gcp and protocol complianceUses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific actions; immediately communicates/escalates serious issues to the project team and with guidance develops action plansDevelops a working knowledge and operates according to ich/gcp guidelines or other applicable guidance, relevant regulations, and company sops/processes. May require knowledge of good pharmacoepidemiology practices (gpp) and good epidemiologic practices (gep) guidelines for nis and to adhere to a schedule of data collection from hcps and patients for nis, effectively employing technology for tracking. Assesses the process of obtaining informed consent has been adequately performed and documented for each subject/patient, as required/appropriateDemonstrates diligence in protecting the confidentiality of each subject/patientAssesses factors that might affect subject/patient’s safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. Applies query resolution techniques remotely and provides guidance to site staff as necessary, driving query resolution to closure within agreed timelinesUtilizes available hardware and software to support the effective conduct of the clinical study data review and captureAssesses site compliance with electronic data capture requirements. May perform remote aggregated data review (radar) utilizing the appropriate tools to identify, respond and manage issues in line with the associated work instructions (wi), radar guideline and clinical monitoring plan (cmp)/site management plan (smp) for assigned sites/projectAbility to identify trends within a site, and across a number of sites, escalating issues and trends to, with guidance, develop corrective actions / preventative actions. May assess if investigational product (ip) has been dispensed and administered to subjects/patients according to the protocol, identifying if issues or risks associated with blinded or randomized information related to ip have occurredApplies knowledge of gcp/local regulations and organizational procedures to ensure ip is appropriately (re)labelled, imported and released/returned. Routinely reviews the site section of the trial master file (tmf) or project master file (pmf) in totality for nis for accuracy, timeliness and completenessRequests new/updated documents from the site, as requiredIf remote access is available to an electronic investigator site file (eisf), routinely reviews the eisf for accuracy, timeliness and completenessReconciles contents of the eisf with the tmfEnsures the investigator/physician site is aware of the requirement of archiving essential documents in accordance with local guidelines and regulations. Documents activities via confirmation letters, follow-up letters, trip reports, and other required project documents as per sops and cmp/smpSupports subject/patient recruitment, retention and awareness strategiesEnters data into tracking systems as required to track all observations, ongoing status and assigned action items to resolution. For assigned activities, understands project scope, budgets, and timelines; manages site-level activities / communication to ensure project objectives, deliverables and timelines are metWith oversight and direction, is able to quickly, adapt to changing priorities to achieve goals / targets. Acts as primary liaison with project site personnel or nis reporters, in collaboration with the on-site craEnsures all assigned sites and project-specific site team members are trained and compliant with applicable requirements. Prepares for and attends investigator meetings, advisory committee meetings and/or other sponsor face to face meetingsParticipates in global clinical monitoring/project staff meetings (inclusive of sponsor representation, as applicable) and attends clinical training sessions according to the project specific requirements. Provides guidance at the site and project level towards audit readiness standards and supports preparation for audit and required follow-up actions. For real world and late phase, the cma i may be assigned to the registry coordinating center (rcc)Additional responsibilities include:
O data review, data query resolution and direct data entry of health care provider (hcp) and patient information. O call center-based communications (inbound and outbound) with registry physicians, and/or patients, by utilizing web-based tools and other communication tools to ensure compliance with protocol requirements and relevant guidelines O complete chart abstraction
Qualifications What we’re looking for
Bachelor’s degree or rn in a related field or equivalent combination of education, training and experience Knowledge of good clinical practice/ich guidelines and/or other applicable regulatory requirements Must demonstrate good computer skills and be able to embrace new technologies.. Excellent communication, presentation and interpersonal skills Ability to manage less than 25% travel
Get to know syneos health We are the only full-service biopharmaceutical solutions company in the worldThat means we bring together the best clinical and commercial minds to create a better, smarter, faster way to get medicines into the hands of patients who need it mostLearn more about syneos health.
Additional information: Tasks, duties, and responsibilities as listed in this job description are not exhaustiveThe company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilitiesEquivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the job descriptionThe company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described aboveFurther, nothing contained herein should be construed to create an employment contractOccasionally, required skills/experiences for jobs are expressed in brief termsAny language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the eu equality directive, in relation to the recruitment and employment of its employeesThe company is committed to compliance with the americans with disabilities act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
Primary location: europe - fra-home-based
Job: clinical monitoring
Travel: yes, 25 % of the time
Employee status: regular
Central Monitoring Associate - Sponsor dedicated
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