Manager, Clinical Research Content & Curriculum Writer
$80k - $90kACRP - Association of Clinical Research Professionals
Manager, Clinical Research Content & Curriculum Writer Manager, Clinical Research Content & Curriculum Writer Get AI-powered advice on this job and more exclusive features. ACRP - Association of Clinical Research Professionals provided pay range This range is provided by ACRP - Association of Clinical Research Professionals. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range $80,000.00/yr - $90,000.00/yr Job Summary: Write and manage ACRP training content and programs using content development and curriculum design principles. ACRP seeks an experienced and dynamic Manager, Clinical Research Content & Curriculum Writer to join our Learning & Development team. This person will own, author and manage all content for ACRP training content and programs through the lens of clinical research competencies, skills and curriculum development principles. This role supports instructional design efforts, subject matter experts (SMEs) and learning technology ensuring the efficient execution of learning content. The person in this role is committed to being an active part of a productive, efficient and empowered team. This person has a sincere commitment to the mission and members of ACRP. This is a full-time salaried position at a range of $80,000 - $90,000. Only those candidates exceeding both the education and experience requirements will be considered for the top of the pay range. This role is remote with occasional travel. Position Responsibilities Create, update and manage content for ACRP training programs across various modalities. This includes, but is not limited to, on-demand and live training, webinars and conference materials. Apply learning and development principles to content development and curriculum design. Proactively identify improvements to ensure all materials reflect the latest clinical research guidelines, regulations (e.g. ICH, FDA, JTF) and customer needs. Create and implement quality assurance (QA) processes for content development, maintenance and improvements. Ability to write, manage and organize content at scale. Measure the effectiveness of training initiatives using survey feedback, performance data, and key metrics such as completion rates, engagement levels to update content. Collaborate with subject matter experts (SMEs) and volunteers to ensure content delivery, accuracy and scalability. Know how and when to use AI tools in the content development process. Break down technical concepts into digestible, engaging and interactive learning experiences that drive learner outcomes for clinical research professionals. These include, but are not limited to, clear objectives, scenarios, knowledge checks, quizzes and assessments. Create, implement and maintain content SOPs, style guides and glossaries to ensure consistency and quality. Support the learning technology team in content taxonomy in the LMS and search functionalities. Knowledge, Skill, Experience, and Education Requirements Bachelor’s degree or equivalent experience (four years) in clinical research Minimum of four years' experience in content development, instructional design, curriculum development, and project management. Expert in virtual and in-person training delivery Experience working with SMEs and content-management systems is a plus. Experience working in membership and/or certification associations and their educational programs is highly desirable. Proficiency in instructional design software (e.g., Articulate 360), learning management systems (LMS) and content management (CMS) platforms. Proficiency in using multimedia tools and technologies to support learning experiences required. Knowledge of adult learning theories and instructional design models Ability to work cross-functionally and manage internal stakeholders. Global content management at scale Customer and learner-centric Member of professional organization(s) to keep current on L&D best practices Excellent communication skills, both written and verbal required. Strong organizational skills and the ability to manage multiple projects simultaneously. Working Conditions / Physical Requirements The physical demands and essential functions described here are representative of those that must be met, with or without reasonable accommodation. To request a reasonable accommodation, employees are encouraged to contact the organization’s HR Lead. Work is performed fully remotely; employee interacts with staff remotely and is expected to have member contact (phone and email) and consult with outside organizations and vendors. This position requires prolonged periods of working on a computer, speaking on a phone, using video conferencing, typing, etc. Must be able to lift up to 10 lbs. at a time. Must be able to work some flexible hours, including weekends, particularly related to ACRP’s annual conference. Out-of-state travel may be required at least once a year, specifically related to ACRP’s annual conference. Seniority level Seniority level Mid-Senior level Employment type Employment type Full-time Job function Job function Research, Analyst, and Information Technology Industries Industry Associations Referrals increase your chances of interviewing at ACRP - Association of Clinical Research Professionals by 2x Sign in to set job alerts for “Clinical Research Manager” roles. 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...Seattle Clinical Research Center is seeking a full-time Clinical Research Coordinator to join our research team. Seattle Clinical Research... ...experience with excellent communication skills and the ability to manage multiple projects with strong attention to detail. The CRC’s...Hourly payFull timeRemote workFlexible hours- ...We are looking to add a Clinical Research Professional to a growing study team. The ideal candidate will feel comfortable in a research environment... ...is not available for this role at this time. Duties Manage 1–3 patient visits per day, with periodic admin-focused days...Full time
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- POSITION OVERVIEW The successful Prospect Research Manager partners closely with WETA's fundraising teams (WETA Major Giving, PBS News, Foundations... ...station in the nation’s capital, produces and distributes content that informs, inspires, and enriches lives. As the second-...InternshipWork at officeLocal areaRemote work
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...and a shared dedication to making a difference in the world. Requirements Job Overview The Clinical Research Coordinator 2 (CRC2) is responsible for managing and coordinating 7 out of approximately 55 ongoing clinical trials, Phases I-IV, in the Dept. of Neurology...Hourly payFull timeWork experience placementWork at office$125k - $150k
...Clinical Trial Manager The Clinical Trial Manager (CTM) works closely with various internal team members and vendors as well as clinical... ...the Duties and Responsibilities outlined for Senior Clinical Research Associate, as needed What experience and education do you...Full timeContract workLocal areaNight shift$20.16 - $31.3 per hour
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About the Job General Summary of Position Under moderate supervision of the Manager the Clinical Research Coordinator I is responsible for a variety of activities in support of clinical research studies. The Clinical Research Coordinator I is responsible for the implementation...Work experience placement- Virginia Heart is seeking a Clinical Research Coordinator for our outpatient cardiology setting in Northern Virginia. The role involves planning, directing, and analyzing cardiac drug and device trials while maintaining GCP/ICH guidelines and FDA regulations. The position...Weekend workAfternoon shift
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- Clinical Research Coordinator - Silver Spring, Maryland The Alaka`ina Foundation Family of Companies is looking for a Clinical Research Coordinator... ...resolving inquiries. Experience utilizing clinical trial management systems and databases (e.g., REDCap and Inform). Must be...Weekend workAfternoon shift
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...Inclusion, Employee Advisory Committee) Position Summary The Clinical Research Coordinator will work in office at the Loudoun Office... ...documents, and progress reports. Participates in preparation and management of research budgets and monetary disbursements. Requirements...Full timeTemporary workWork at officeFlexible hoursAfternoon shift- Retina Group of Washington, a PRISM Vision Group Partner Practice, is seeking a Clinical Research Coordinator in Chevy Chase, MD. This full-time, exempt role supports the Manager of Clinical Research by coordinating and conducting studies, collecting data, and ensuring...Full timeWork at office
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