Pfizer
Clinical Research Associate
Pfizer, New Haven, Connecticut, us, 06540
Clinical Study Participant Coordinator (Contract)
Contract (17 months 28 days)Published a day agoClinical Study Participant CoordinatorSummary:The Volunteer Recruitment Support Associate is responsible for registering new and current clinical research participants and conducting a series of pre-screening procedures to determine eligibility and enroll them for clinical studies. The Volunteer Recruitment Support executes recruitment strategies and acts in compliance with regulatory requirements related to the protection of all participants' confidential data. Additional responsibilities may include serving as a preceptor for new staff in training and participating in projects within the department related to participant outreach, metrics, and database optimization.Responsibilities:Maintain first contact with potential participants and inform them about clinical research and available study opportunities.Communicate protocol requirements, study procedures, stipend information, and PCRU policies to potential participants in a prompt and professional manner.Assess participant's qualifications for participation in a study based on information gathered during the intake in accordance with study protocol inclusion/exclusion criteria and medical guidance.Maintain source documentation, accuracy, accessibility, and confidentiality of participant records and reports.Communicate with participants via text messaging, emailing, and other methods in compliance with regulatory requirements for study-related recruitment, follow-up, soliciting updated information, and regular database clean up.Schedule study screenings and cohorts/groups for dosing according to established timelines and manage appointments.Demonstrate a positive attitude to the participant population to ensure trust in clinical research.Perform database cleanup activities and other recruitment and targeted outreach projects.May train and mentor new staff members.May perform cross-functional responsibilities within the recruitment department, such as participant payments, marketing, website development, and social media.Qualifications:High school diploma / GED with a minimum of 3+ years of experience in a clinical setting OR;Health care practice experience with a valid license (RN, LPN) OR;A minimum of 1+ years of experience in clinical research recruitment OR;Bachelor's degree in Nursing, Public Health, Life Sciences, or equivalent experience.Experience with electronic healthcare records.Medical office experience required.Experience with medical terminology and clinical mindset.Ability to multi-task within multiple systems/databases.Ability to maintain a high level of morality or professionalism.Independent thinker and decision-making ability.Strong written and oral communication skills.Adept knowledge of medical terminology preferred.Experience with ICH-GCP guidelines, and patient confidentiality preferred.Rate/Hours:$33 - $38 per hour.This is a fully onsite position located in New Haven, CT.Must be available and flexible to work all of the following shifts:Monday - Thursday: 7:30 AM - 4:00 PM; 9:00 AM - 5:30 PM; 10:00 AM - 6:30 PM.Friday: 7:30 AM - 4:00 PM; 8:00 AM - 4:30 PM; 9:00 AM - 5:30 PM.Saturday: As needed per level of recruitment activity. Would be given advance notice if Saturday work is needed.Please note contractors are engaged to provide services to Pfizer on a temporary basis in connection with a specific assignment. Contractors are hired and employed through Atrium, our third-party payrolling partner.This job posting is for a temporary role as an employee of Atrium on assignment at Pfizer. The individual selected for this role will be offered the role as an employee of Atrium; compensation, medical benefits, fringe benefits, and other terms and conditions of employment shall be presented by Atrium upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors, including skills, competencies, experience, location and/or being pursued, and other job-related factors permitted by law. In addition, this role will be eligible for overtime pay, in accordance with federal and state requirements.
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Contract (17 months 28 days)Published a day agoClinical Study Participant CoordinatorSummary:The Volunteer Recruitment Support Associate is responsible for registering new and current clinical research participants and conducting a series of pre-screening procedures to determine eligibility and enroll them for clinical studies. The Volunteer Recruitment Support executes recruitment strategies and acts in compliance with regulatory requirements related to the protection of all participants' confidential data. Additional responsibilities may include serving as a preceptor for new staff in training and participating in projects within the department related to participant outreach, metrics, and database optimization.Responsibilities:Maintain first contact with potential participants and inform them about clinical research and available study opportunities.Communicate protocol requirements, study procedures, stipend information, and PCRU policies to potential participants in a prompt and professional manner.Assess participant's qualifications for participation in a study based on information gathered during the intake in accordance with study protocol inclusion/exclusion criteria and medical guidance.Maintain source documentation, accuracy, accessibility, and confidentiality of participant records and reports.Communicate with participants via text messaging, emailing, and other methods in compliance with regulatory requirements for study-related recruitment, follow-up, soliciting updated information, and regular database clean up.Schedule study screenings and cohorts/groups for dosing according to established timelines and manage appointments.Demonstrate a positive attitude to the participant population to ensure trust in clinical research.Perform database cleanup activities and other recruitment and targeted outreach projects.May train and mentor new staff members.May perform cross-functional responsibilities within the recruitment department, such as participant payments, marketing, website development, and social media.Qualifications:High school diploma / GED with a minimum of 3+ years of experience in a clinical setting OR;Health care practice experience with a valid license (RN, LPN) OR;A minimum of 1+ years of experience in clinical research recruitment OR;Bachelor's degree in Nursing, Public Health, Life Sciences, or equivalent experience.Experience with electronic healthcare records.Medical office experience required.Experience with medical terminology and clinical mindset.Ability to multi-task within multiple systems/databases.Ability to maintain a high level of morality or professionalism.Independent thinker and decision-making ability.Strong written and oral communication skills.Adept knowledge of medical terminology preferred.Experience with ICH-GCP guidelines, and patient confidentiality preferred.Rate/Hours:$33 - $38 per hour.This is a fully onsite position located in New Haven, CT.Must be available and flexible to work all of the following shifts:Monday - Thursday: 7:30 AM - 4:00 PM; 9:00 AM - 5:30 PM; 10:00 AM - 6:30 PM.Friday: 7:30 AM - 4:00 PM; 8:00 AM - 4:30 PM; 9:00 AM - 5:30 PM.Saturday: As needed per level of recruitment activity. Would be given advance notice if Saturday work is needed.Please note contractors are engaged to provide services to Pfizer on a temporary basis in connection with a specific assignment. Contractors are hired and employed through Atrium, our third-party payrolling partner.This job posting is for a temporary role as an employee of Atrium on assignment at Pfizer. The individual selected for this role will be offered the role as an employee of Atrium; compensation, medical benefits, fringe benefits, and other terms and conditions of employment shall be presented by Atrium upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors, including skills, competencies, experience, location and/or being pursued, and other job-related factors permitted by law. In addition, this role will be eligible for overtime pay, in accordance with federal and state requirements.
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