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