A Clinical Research Associate manages clinical trials and studies related to pharmaceutical and biotechnological products, drugs and procedures. Protecting subjects’ confidentiality, updating their information, and verifying IP has been dispensed and administered according to protocol. 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. Or they may work with several different sponsors and protocols. Proficient with Microsoft Office Word, Excel and Power Point. Clinical Research Analysts play an essential role in all forms of medical research including early and late phase clinical trials. Professional Research Associate Job Description Template Research associates help companies increase workload and improve products. A Clinical Research Associate, also known as a CRA, conducts research to ensure these products are safe to allow on the market. 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. Clinical research associates work in various settings, such as pharmaceutical companies, medical research institutes and government agencies. Before coming up with a favorable salary for your Clinical Research Associate, ensure you confirm with other companies in your location. This salary is subject to variation depending on size of a company and its geographical location. 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 … Make sure to customize it to include your company’s specific requirements and responsibilities. Use these job description examples to create your next great job posting. 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. Sort by: relevance - date. Apply to Clinical Research Associate and more! Overseeing and documenting IP dispensing, inventory and reconciliation. Skills and Qualifications prove that an individual is capable of performing at a job. Students searching for Clinical Research Associate: Job Duties & Info found the following related articles, links, and information useful. Job Summary § Administration and full investigator site responsibility for clinical studies according to ORION Hey there! Strong verbal and written communication skills. Whichever path they take, CRAs benefit from unparalleled opportunities, experience, and rewards. Bachelor’s degree in Biological Science or a related field. 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. Knowledge of FDA regulatory requirements is required. We are looking for an organized, flexible Clinical Research Associate to oversee clinical trials. Ideal candidates will be detail-oriented, have the ability to multitask and be able to collaborate with various role players. Clinical Research Assistants play an important role in clinical trials as they perform the actual testing of medications and medical devices. They may participate in … 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. The Clinical Research Associate will develop and outline trial protocols, establish trial sites, train site staff, and manage Investigational Product (IP) and trial materials. 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. They bring in their medical and scientific knowledge, analytical abilities, and research expertise to the job. Ensuring compliance with SOPs and local regulations, and ICH and GCP guidelines. Identifying, evaluating and establishing trial sites, and closing sites down on completion of trial. Writes protocols, case report forms, and consent forms. 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 … Being a Clinical Research Associate I ensures compliance with protocol and overall clinical objectives. 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 Supervise employees engaged in clinical research under your purview Need help writing a job description for a specific role? A Clinical Research Associate’s experience requirements are necessary to prove their expertise in the profession. 2+ years experience as a Clinical Research Associate. Training site staff on therapeutic areas, protocol requirements, proper source documentation and case report form completion. Identifying, evaluating and establishing trial sites, and closing sites down on completion of trial. Other tasks and responsibilities as needed. Creating and writing trial protocols, and presenting these to steering committee. *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 These requirements indicate that a Clinical Research Associate has sufficient knowledge and training to excel at the job. To be successful in this role, you should be able to recognize logistical problems, and initiate appropriate solutions. Job Summary Responsible for creating, implementing, and maintaining clinical trials. Knowledge of pharmaceutical industry, terminology and practices. • Liaise with site personnel regarding the conduct of Second Sight clinical trials. The average salary for a Clinical Research Associate (CRA) in Toronto, Ontario is C$60,459. This Clinical Research Associate job description sample can help you hire an innovative and experienced Clinical Research Associate to your firm. Clinical Research Associates also compile and finalize reports from long-term clinical trials. A Clinical Research Associate should also have experience in dealing with medical research software. Clinical Research Associate Responsibilities: Creating and writing trial protocols, and presenting these to steering committee. PRA Clinical Research Associates (CRAs) choose one of two career paths. Recruits and selects investigators and ensures good clinical practices are followed. Search 45 Clinical Research Clinical QA jobs now available on Indeed.com, the world's largest job site. Conducting regular site visits, coordinating project meetings and writing visit reports. Post a Clinical Research Associate job to 100 job boards with one submission. Indeed may be compensated by these employers, helping keep Indeed free for job seekers. Typically, a clinical research associate does not have direct contact with the participants involved with the study. Completely free trial, no credit card required. They gather data, design tests and help ensure that information is being properly recorded and assessed. 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. Including requirements, responsibilities, statistics, industries, similar jobs and job openings for Clinical Research Associate I. 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. Clinical-Research Associate (CRA) Reports to: Project Manager or Clinical-Research Site Manager. Manage regulatory authority applications and approvals that oversee the research and marketing of … Analyze and evaluate clinical data gathered during research. Analyzes and evaluates clinical data gathered during research. Proper fulfillment of a Clinical Research Associate’s duties and responsibilities brings success to your company. Completely free trial, no credit card required. Displayed here are job ads that match your query. Compare salaries and apply for all the clinical research associate jobs in canada. Ensure compliance with protocol and overall clinical objectives. Page 1 of 375 jobs. A Clinical Research Associate should have a bachelor’s degree in life sciences such as biochemistry, biology, microbiology and pharmacology. 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. 867 Clinical Research Associate jobs available on Indeed.com. A Clinical Research Associate should have extensive experience in clinical data work, clinical laboratory work, nursing, academic or pharmaceutical research and medical sales. 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. Education and training requirements are an essential part of your job description. Liaise with ethics committee regarding rights, safety and well-being of trial subjects. 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. Alternatively, they may have a graduate or a postgraduate degree in medical sciences like immunology, anatomy, physiology and medicine. 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 jobs. Post to over 100+ job boards. Or if you’re ready to hire, post your job on Indeed. A Clinical Research Associate manages clinical trials and studies related to pharmaceutical and biotechnological products, drugs and procedures. Post a Clinical Research Associate job to 100 job boards with one submission. Browse 325 CANADA CLINICAL RESEARCH ASSOCIATE job listings from companies with openings that are hiring right now! A competent Clinical Research Associate should be able to perform various duties and responsibilities. Post Jobs for FREE. Valid driver’s license, proficient driving skills, own reliable transport and up-to-date car insurance. Implementing action plans for sites not meeting expectations. They may also have experience serving as clinical coordinators or clinical trials administrators. You will conduct regular site visits, generate and distribute internal and external newsletters, prepare final reports and liaise with interested parties regarding all trial aspects. Clinical Research Associates manage clinical trials and studies pertaining to biotechnological and pharmaceutical products, drugs and procedures. Ordering, tracking, and managing IP and trial materials. 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. Competencies Interpersonal Relationships Ability to build trust with site personnel and communicate with concerned personnel. Teamwork Ability to work cooperatively as part of a team. *Indeed provides this information as a courtesy to users of this site. Reach over 150 million candidates. Available to travel extensively and on short notice, and ability to manage travel schedules, such as flight schedules. Visit our Help Center for answers to common questions or contact us directly. They may work onsite with one of our top pharmaceutical clients. Clinical Research Associate Interview Questions, Clinical Research Associate Resume [Guide + Free Template]. Knowledge of FDA regulations and their practical implementation. Clinical Research Associate I participates in the design, administration and monitoring of clinical trials. Indeed ranks Job Ads based on a combination of employer bids and relevance, such as your search terms and other activity on Indeed. Clinical Research Associates should assist in organizing and monitoring the different stages of clinical trials. Including this category in your description can help you attract a high quality Clinical Research Associate. Quickly find and apply for your next job opportunity on Workopolis. The Clinical Research Associate will manage multiple aspects of subjects' welfare. 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… A Clinical Research Associate may also be proficient with scientific software like InferMed MARCO Electronic Data Capture or StataCorp Stata. Research Assistant Job Description Participate in the design, administration and monitoring of clinical trials. 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. In case this is not quite the job description you were looking for, we have other similar job descriptions that might meet your requirements. You will play a leading role in generating and overseeing documentation and records. Job description for Clinical Research Associate I. 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. Ability to manage and prioritize workload effectively. While you're here, why don't you post your job to Indeed! 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 . 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