Students searching for Clinical Research Associate: Job Duties & Info found the following related articles, links, and information useful. Or they may work with several different sponsors and protocols. Clinical Research Associates also compile and finalize reports from long-term clinical trials. Writes protocols, case report forms, and consent forms. Clinical Research Associate Interview Questions, Clinical Research Associate Resume [Guide + Free Template]. Professional Research Associate Job Description Template Research associates help companies increase workload and improve products. Clinical-Research Associate (CRA) Reports to: Project Manager or Clinical-Research Site Manager. A Clinical Research Associate manages clinical trials and studies related to pharmaceutical and biotechnological products, drugs and procedures. Job description ClinTec International is actively recruiting for a Clinical Research Associate to join our expanding global company across the South Eastern African region – with sites in Zambia, Mozambique, Uganda, Kenya and Tanzania . Clinical Research Associates should assist in organizing and monitoring the different stages of clinical trials. Indeed may be compensated by these employers, helping keep Indeed free for job seekers. The clinical research associate is in charge of developing the trial system and protocol (in research parlance: the methodology), set up the lab or the centre that will be the location of the study, verify and collect the data that is used for and collected from the study, and, in the end, write the reports that present the final result of the study. Apply to Clinical Research Associate and more! Search 45 Clinical Research Clinical QA jobs now available on Indeed.com, the world's largest job site. Manage regulatory authority applications and approvals that oversee the research and marketing of … A competent Clinical Research Associate should be able to perform various duties and responsibilities. Ensure compliance with protocol and overall clinical objectives. The Clinical Research Associate will develop and outline trial protocols, establish trial sites, train site staff, and manage Investigational Product (IP) and trial materials. A Clinical Research Associate should also have experience in dealing with medical research software. Clinical Research Associate I participates in the design, administration and monitoring of clinical trials. These include: Ready to hire a Clinical Research Associate? A Clinical Research Associate should have a bachelor’s degree in life sciences such as biochemistry, biology, microbiology and pharmacology. Ordering, tracking, and managing IP and trial materials. Displayed here are job ads that match your query. Indeed ranks Job Ads based on a combination of employer bids and relevance, such as your search terms and other activity on Indeed. While you're here, why don't you post your job to Indeed! Implementing action plans for sites not meeting expectations. This salary is subject to variation depending on size of a company and its geographical location. Valid driver’s license, proficient driving skills, own reliable transport and up-to-date car insurance. They may also have experience serving as clinical coordinators or clinical trials administrators. Sort by: relevance - date. Clinical Research Associates manage clinical trials and studies pertaining to biotechnological and pharmaceutical products, drugs and procedures. Knowledge of FDA regulations and their practical implementation. Other tasks and responsibilities as needed. Clinical Research Associate 2 - VCC - VICTR **REMOTE AVAILABLE**This is a full-time/exempt term position lasting six months to one year.JOB SUMMARYThis position is responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of stud Recruits and selects investigators and ensures good clinical practices are followed. Build a Clinical Research Associate job description, Art Director Job Description | Indeed.com, Assistant Teacher Job Description Sample | Indeed.com, Caseworker Job Description Sample | Indeed.com, CTO Chief Technology Officer Job Description Sample | Indeed, Diesel Mechanic Job Description Sample | Indeed, Director of Sales Job Description Sample | Indeed.com, Logistics Specialist Coordinator Job Description Sample | Indeed, Manufacturing Engineer Job Description Sample | Indeed, Marketing Director Job Description Sample | Indeed, Medical Technologist Job Description Sample | Indeed, Millwright Job Description Sample | Indeed, Network Administrator Job Description Sample| Indeed, Outside Sales Representative Job Description Sample | Indeed.com, Patient Care Technician Job Description Sample | Indeed, Phlebotomist Job Description Sample | Indeed, Prep Cook Job Description Sample | Indeed, Procurement Manager Job Description Sample | Indeed.com, Production Supervisor Job Description Sample | Indeed, Program Coordinator Job Description Sample | Indeed, Real Estate Agent Job Description Sample | Indeed, Software Engineer Job Description Sample | Indeed, Sous Chef Job Description Sample | Indeed.com, Tax Preparer Job Description Sample | Indeed.com, Supervise study sites and activities to ensure adherence to appropriate industry protocols and terms of the study, Collect and authenticate data collection forms otherwise known as case report forms, Screen potential study participants through medical record reviews, interviews and follow-ups with healthcare providers, Coordinate with ethics committees to safeguard the rights, safety and wellbeing of all research subjects and research activities, Maintain specific records of research activity to include regulatory forms, drug dispensation records, case reports and consent forms, Prepare final reports, occasional manuscripts or publication, New Drug Applications (NDAs) and Biological License Applications (BLAs), Ensure proper transmission of clinical case data to the data management centers, review case reports questions and problems and clarify or obtain alterations to data as appropriate, Oversee research, technical and administrative staff, to include training, hiring, goal setting and distribution of workload, Strong written and oral communication skills, Ability to build effective relationships with trial center colleagues and staff, Superior problem solving, deductive reasoning and decision-making skills, Good time management and ability to prioritize tasks and accomplish set goals efficiently, Knowledge of statistical data collection, validation, editing and analysis techniques, Ability to provide technical guidance, advice and support to professional staff where needed, Knowledge of laboratory certification processes and standards, Excellent attention to detail and ability to maintain detailed and accurate records. Clinical research associates work in various settings, such as pharmaceutical companies, medical research institutes and government agencies. Available to travel extensively and on short notice, and ability to manage travel schedules, such as flight schedules. Job Profile – Clinical Research Associate I/II (CRA) Role Profile – Orion I/II CRA Page 3 of 5 Version Date: 12 January 2015 PART 3 – JOB DESCRIPTION - JOB FUNCTION 1. Please note that we are not your recruiting or legal advisor, we are not responsible for the content of your job descriptions, and none of the information provided herein guarantees performance. Clinical Research Associate jobs. In case this is not quite the job description you were looking for, we have other similar job descriptions that might meet your requirements. Bachelor’s degree in Biological Science or a related field. They are in charge of recruiting study participants, collecting patient data, creating study documentation and conducting quality assurance audits to ensure study protocols are in order. Skills and Qualifications prove that an individual is capable of performing at a job. *Indeed provides this information as a courtesy to users of this site. Senior Clinical Research Associate (Sr. CRA) ESSENTIAL DUTIES AND RESPONSIBILITIES: • Ensure that the clinical trials are being conducted in accordance with the clinical protocol, national regulations, international standards, and Second Sight procedures. Knowledge of FDA regulatory requirements is required. This Clinical Research Associate job description sample can help you hire an innovative and experienced Clinical Research Associate to your firm. These requirements indicate that a Clinical Research Associate has sufficient knowledge and training to excel at the job. Here as some skills and qualifications to look for in your Clinical Research Associate: The national average salary for a Clinical Research Associate is $79,359. Post a Clinical Research Associate job to 100 job boards with one submission. 2+ years experience as a Clinical Research Associate. *Job Description: * The Associate, Regulatory Affairs will be responsible for assisting with clinical trial applications, new registrations, license… Estimated: $57,000 - $82,000 a year 3 days ago Including this category in your description can help you attract a high quality Clinical Research Associate. Reach over 150 million candidates. Overseeing and documenting IP dispensing, inventory and reconciliation. Knowledge of pharmaceutical industry, terminology and practices. An associate's degree is required to get a job as a clinical research analyst, and a bachelor's or master's degree is preferred for higher level positions. Make sure to customize it to include your company’s specific requirements and responsibilities. Typical employers include pharmaceutical companies or contract research organisations (CROs), which conduct research on behalf of pharmaceutical companies.A CRO will organise the placement of a CRA on behalf of the sponsor (the pharmaceutical company) and may be involved in planning, organising and conducting the whole study or just part of it. Clinical Research Associate Responsibilities: Creating and writing trial protocols, and presenting these to steering committee. Job Summary Responsible for creating, implementing, and maintaining clinical trials. They gather data, design tests and help ensure that information is being properly recorded and assessed. Being a Clinical Research Associate I ensures compliance with protocol and overall clinical objectives. Job Description As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality… in feasibility research Support regulatory team in preparing … Identifying, evaluating and establishing trial sites, and closing sites down on completion of trial. Quickly find and apply for your next job opportunity on Workopolis. A Clinical Research Associate may also be proficient with scientific software like InferMed MARCO Electronic Data Capture or StataCorp Stata. A Clinical Research Associate’s experience requirements are necessary to prove their expertise in the profession. Clinical Research Assistants play an important role in clinical trials as they perform the actual testing of medications and medical devices. The average salary for a Clinical Research Associate (CRA) in Toronto, Ontario is C$60,459. We are looking for an organized, flexible Clinical Research Associate to oversee clinical trials. Job Summary § Administration and full investigator site responsibility for clinical studies according to ORION A Clinical Research Associate should have extensive experience in clinical data work, clinical laboratory work, nursing, academic or pharmaceutical research and medical sales. PRA Clinical Research Associates (CRAs) choose one of two career paths. Proper fulfillment of a Clinical Research Associate’s duties and responsibilities brings success to your company. Education and training requirements are an essential part of your job description. You will play a leading role in generating and overseeing documentation and records. Competencies Interpersonal Relationships Ability to build trust with site personnel and communicate with concerned personnel. Sr CRA - Montreal, Canada - Oncology (Solid Tumor) - (20007614) Description JOB SUMMARY The Clinical Research Associate II (CRA II…) will perform monitoring and site management activities for Phase I-IV clinical research projects to assess the progress of clinical projects at assigned investigative/physician sites… Browse 325 CANADA CLINICAL RESEARCH ASSOCIATE job listings from companies with openings that are hiring right now! Post to over 100+ job boards. Training site staff on therapeutic areas, protocol requirements, proper source documentation and case report form completion. Including requirements, responsibilities, statistics, industries, similar jobs and job openings for Clinical Research Associate I. Compare salaries and apply for all the clinical research associate jobs in canada. Clinical Research Associate also known as monitor is employed by either a pharmaceutical company or a contract research organization (CRO) which works on behalf of pharmaceutical companies. • Liaise with site personnel regarding the conduct of Second Sight clinical trials. Completely free trial, no credit card required. Clinical trials may be carried out at various phases, trials on patients with a disease, and studies conducted after the launch of a new drug to monitor safety and side effects. Supervise employees engaged in clinical research under your purview Ensuring compliance with SOPs and local regulations, and ICH and GCP guidelines. Completely free trial, no credit card required. Protecting subjects’ confidentiality, updating their information, and verifying IP has been dispensed and administered according to protocol. Before coming up with a favorable salary for your Clinical Research Associate, ensure you confirm with other companies in your location. Page 1 of 375 jobs. Use these job description examples to create your next great job posting. The following are other duties and responsibilities a Clinical Research Associate should be able to execute: A Clinical Research Associate will have certain skills and qualifications. Proficient with Microsoft Office Word, Excel and Power Point. Identifying, evaluating and establishing trial sites, and closing sites down on completion of trial. Clinical Research Analysts play an essential role in all forms of medical research including early and late phase clinical trials. Post a Clinical Research Associate job to 100 job boards with one submission. Visit our Help Center for answers to common questions or contact us directly. However, CRAs must be able to work in a collaborative environment, coming into frequent contact with the clinical team at the study site and the supervisors from the study sponsor. They are in charge of recruiting study participants, collecting patient data, creating study documentation and conducting quality assurance audits to ensure study protocols are in order. JOB DESCRIPTION – CLINICAL RESEARCH ASSOCIATE Description Job Title Clinical Research Associate Reports to Title VP Clinical Affairs General Accountability Our mission is to Profoundly change the standard of care by creating a tomorrow where clinicians can … Need help writing a job description for a specific role? Ideal candidates will be detail-oriented, have the ability to multitask and be able to collaborate with various role players. They may work onsite with one of our top pharmaceutical clients. Post Jobs for FREE. Or if you’re ready to hire, post your job on Indeed. Conducting regular site visits, coordinating project meetings and writing visit reports. Whichever path they take, CRAs benefit from unparalleled opportunities, experience, and rewards. Liaise with ethics committee regarding rights, safety and well-being of trial subjects. Analyzes and evaluates clinical data gathered during research. They may participate in … Hey there! Ability to manage and prioritize workload effectively. A Clinical Research Associate manages clinical trials and studies related to pharmaceutical and biotechnological products, drugs and procedures. The Clinical Research Associate will manage multiple aspects of subjects' welfare. A clinical research associate (CRA), also called a clinical monitor or trial monitor, is a health-care professional who performs many activities related to medical research, particularly clinical trials. Usual duties mentioned on a Clinical Research Assistant resume include organizing files, handling correspondence, implementing operating procedures, following guidelines from ethics committees, and updating databases. Creating and writing trial protocols, and presenting these to steering committee. Research Assistant Job Description Participate in the design, administration and monitoring of clinical trials. Teamwork Ability to work cooperatively as part of a team. A Clinical Research Associate, also known as a CRA, conducts research to ensure these products are safe to allow on the market. They bring in their medical and scientific knowledge, analytical abilities, and research expertise to the job. Typically, a clinical research associate does not have direct contact with the participants involved with the study. Alternatively, they may have a graduate or a postgraduate degree in medical sciences like immunology, anatomy, physiology and medicine. Analyze and evaluate clinical data gathered during research. To be successful in this role, you should be able to recognize logistical problems, and initiate appropriate solutions. Strong verbal and written communication skills. 867 Clinical Research Associate jobs available on Indeed.com. 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