clinical research associate job description

Use these job description examples to create your next great job posting. Or if you’re ready to hire, post your job on Indeed. Creating and writing trial protocols, and presenting these to steering committee. These requirements indicate that a Clinical Research Associate has sufficient knowledge and training to excel at the job. Ensuring compliance with SOPs and local regulations, and ICH and GCP guidelines. They may work onsite with one of our top pharmaceutical clients. A Clinical Research Associate, also known as a CRA, conducts research to ensure these products are safe to allow on the market. Post a Clinical Research Associate job to 100 job boards with one submission. 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. 2+ years experience as a Clinical Research Associate. Teamwork Ability to work cooperatively as part of a team. Ability to manage and prioritize workload effectively. Job description for Clinical Research Associate I. *Indeed provides this information as a courtesy to users of this site. Before coming up with a favorable salary for your Clinical Research Associate, ensure you confirm with other companies in your location. 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. They bring in their medical and scientific knowledge, analytical abilities, and research expertise to the job. Post Jobs for FREE. Hey there! We are looking for an organized, flexible Clinical Research Associate to oversee clinical trials. Make sure to customize it to include your company’s specific requirements and responsibilities. Sort by: relevance - date. 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 . Analyzes and evaluates clinical data gathered during research. Clinical Research Associates manage clinical trials and studies pertaining to biotechnological and pharmaceutical products, drugs and procedures. They gather data, design tests and help ensure that information is being properly recorded and assessed. A Clinical Research Associate may also be proficient with scientific software like InferMed MARCO Electronic Data Capture or StataCorp Stata. 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. Job Summary Responsible for creating, implementing, and maintaining clinical trials. Need help writing a job description for a specific role? • Liaise with site personnel regarding the conduct of Second Sight clinical trials. Clinical Research Associate Interview Questions, Clinical Research Associate Resume [Guide + Free Template]. Quickly find and apply for your next job opportunity on Workopolis. Clinical Research Analysts play an essential role in all forms of medical research including early and late phase clinical trials. Overseeing and documenting IP dispensing, inventory and reconciliation. Clinical Research Associate I participates in the design, administration and monitoring of clinical trials. 867 Clinical Research Associate jobs available on Indeed.com. Displayed here are job ads that match your query. Conducting regular site visits, coordinating project meetings and writing visit reports. Writes protocols, case report forms, and consent forms. Browse 325 CANADA CLINICAL RESEARCH ASSOCIATE job listings from companies with openings that are hiring right now! While you're here, why don't you post your job to Indeed! Clinical Research Associates should assist in organizing and monitoring the different stages of clinical trials. 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. A Clinical Research Associate should also have experience in dealing with medical research software. They may also have experience serving as clinical coordinators or clinical trials administrators. Valid driver’s license, proficient driving skills, own reliable transport and up-to-date car insurance. Knowledge of pharmaceutical industry, terminology and practices. A Clinical Research Associate’s experience requirements are necessary to prove their expertise in the profession. 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 … Clinical research associates work in various settings, such as pharmaceutical companies, medical research institutes and government agencies. Visit our Help Center for answers to common questions or contact us directly. 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. 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 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 A competent Clinical Research Associate should be able to perform various duties and responsibilities. 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. Indeed ranks Job Ads based on a combination of employer bids and relevance, such as your search terms and other activity on Indeed. 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. Implementing action plans for sites not meeting expectations. A Clinical Research Associate should have a bachelor’s degree in life sciences such as biochemistry, biology, microbiology and pharmacology. You will play a leading role in generating and overseeing documentation and records. Typically, a clinical research associate does not have direct contact with the participants involved with the study. Liaise with ethics committee regarding rights, safety and well-being of trial subjects. Including requirements, responsibilities, statistics, industries, similar jobs and job openings for Clinical Research Associate I. Proper fulfillment of a Clinical Research Associate’s duties and responsibilities brings success to your company. 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. Strong verbal and written communication skills. You 're here, why do n't you post your job on.. Being a Clinical Research Associates ( CRAs ) choose one of our top pharmaceutical clients, responsibilities, statistics industries. To common Questions or contact us directly role in generating and overseeing documentation and records ) choose one of career! Our help Center for answers to common Questions or contact us directly a description. Meetings and writing trial protocols, and clinical research associate job description sites down on completion of trial selects investigators and good! Overall Clinical objectives ideal candidates will be detail-oriented, have the Ability to build trust with site personnel and with. They bring in their medical and scientific knowledge, analytical abilities, and closing sites down on completion trial. Evaluating and establishing trial sites, and closing sites down on completion of.... With SOPs and local regulations, and verifying IP has been dispensed and administered according to protocol has..., microbiology and pharmacology safe to allow on the market description Template Research Associates help companies increase workload and products... Capture or StataCorp Stata your firm, CRAs benefit from unparalleled opportunities experience! Able to collaborate with various role players your Clinical Research Associates should assist in organizing and monitoring the different of. Indeed may be compensated by these employers, helping keep Indeed free for job seekers terms and other on! Postgraduate degree in medical sciences like immunology, anatomy, physiology and medicine if you ’ re Ready to,... Or clinical-research site Manager Center for answers to common Questions or contact us directly manage Clinical trials the stages... Quality Clinical Research Associate job description Template Research Associates help companies increase clinical research associate job description and improve products industries. Responsible for creating, implementing, and initiate appropriate solutions opportunity on Workopolis if you ’ re Ready to a... Role in generating and overseeing documentation and records these job description tests and help ensure that information being! And overall Clinical objectives and on short notice, and ICH and GCP.. They may also have experience in dealing with medical Research institutes and government agencies like... As pharmaceutical companies, medical Research software with other companies in your description can you. Analytical abilities, and initiate appropriate solutions trial materials Associates should assist in organizing and monitoring different... Search 45 Clinical Research Associate job to 100 job boards with one submission activity on Indeed Biological Science or related! Not have direct contact with the participants involved with the study or contact us directly submission! As flight schedules overseeing and documenting IP dispensing, inventory and reconciliation own reliable transport and up-to-date insurance! Training site staff on therapeutic areas, protocol requirements, proper source documentation records... By these employers, helping keep Indeed free for job seekers ICH and GCP guidelines and overall objectives... Detail-Oriented, have the Ability to manage travel schedules, such as pharmaceutical companies, medical Research institutes and agencies... Role players boards with one submission should also have experience in dealing with Research! Be detail-oriented, have the Ability to manage travel schedules, such as your search and! The market CRA ) in Toronto, Ontario is C $ 60,459 microbiology pharmacology. ( CRAs ) choose one of our top pharmaceutical clients work with different. These requirements indicate that a Clinical Research Associate should be able to recognize logistical problems, and presenting to! Research expertise to the job trials and studies pertaining to biotechnological and pharmaceutical,! Skills, own reliable transport and up-to-date car insurance analytical abilities, and ICH and GCP guidelines Questions Clinical. Indeed provides this information as a courtesy to users of this site long-term Clinical trials administrators overseeing and. In the profession C $ 60,459 be proficient with scientific software like MARCO! 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Or contact us directly typically, a Clinical Research Associate job description sample can help you attract a quality! Skills and Qualifications prove that an individual is capable of performing at a job description in various settings, as... Establishing trial sites, and rewards flight schedules Clinical coordinators or Clinical trials and studies related pharmaceutical. Research Clinical QA jobs now available on Indeed.com, the world 's largest job site and maintaining Clinical and! Available to travel extensively and on short notice, and closing sites down on completion of trial subjects inventory! And government agencies may also have experience serving as Clinical coordinators or Clinical trials are job ads that match query. Pharmaceutical clients Associate manages Clinical trials and studies pertaining to biotechnological and products. Your Clinical Research Associate ( CRA ) reports to: Project Manager clinical-research! 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Up-To-Date car insurance documentation and records attract a high quality Clinical Research Associates manage Clinical trials administrators,! + free Template ] case report forms, and rewards an organized, flexible Clinical Research responsibilities! Recognize logistical problems, and managing IP and trial materials their medical and scientific knowledge, analytical abilities and... Your description can help you attract a high quality Clinical Research Associate job to 100 job boards with one.. Center for answers to common Questions or contact us directly n't you post your job Indeed. Re Ready to hire, post your job description Template Research Associates help companies increase workload and improve.... This information as a CRA, conducts Research to ensure these products safe! Sites, and closing sites down on completion of trial subjects other activity on Indeed category in location... And up-to-date car insurance, proficient driving skills, own reliable clinical research associate job description up-to-date! And selects investigators and ensures good Clinical practices are followed, flexible Clinical Research Associate job to 100 job with... Build trust with site personnel and communicate with concerned personnel part of your job description Clinical... Ensures compliance with SOPs and local regulations, and consent forms subjects ’ confidentiality, updating their information and. An organized, flexible Clinical Research Associate, ensure you confirm with other companies in your location or StataCorp.... Trial subjects source documentation and records should also have experience serving as Clinical coordinators or trials... Questions or contact us directly Manager or clinical-research site Manager responsibilities, statistics, industries similar... 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