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. Senior Clinical Quality Assurance Auditor Senior Clinical Quality Assurance Auditor Washington, DC $80,000.00-$110,000.00 4 days ago District of Columbia, United States 20 hours ago Professional Ortho Surgical Medical Coder - Remote District of Columbia, United States 1 week ago We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr ACRP - Association of Clinical Research Professionals
- ...cancer, the American Society of Clinical Oncology (ASCO) is committed to conquering cancer through research, education, and promotion of... ...Operationalize AI-assisted content analysis by executing standardized... ...education. Strong time management and organizational skills, with...SuggestedWork at officeWorldwideFlexible hours
- ...login before you can apply for a job. Clinical Research Medical Director - Hematology Oncology... ...relationships Support product lifecycle management for new indications as directed by Global Development Lead Provide clinical content input to materials to be used in Scientific...SuggestedRemote workFlexible hours
$25 - $35 per hour
...Job Description Job Description Job Title: Clinical Research Coordinator Hours: 30 hours per week (Monday-Friday) Contract duration... ...Coordinator role supports a balance impairment study by managing study data and ensuring accurate documentation within the electronic...SuggestedContract workTemporary workPart timeMonday to Friday- ...Job Description Job Description Description: Clinical Trial & Pharmacovigilance Manager Location: Hybrid Job Type: Full-Time About the... ...submissions Qualifications ~ Advanced degree in clinical research, life sciences, or healthcare field ~8+ years of...SuggestedFull time
- ...Medicine Strategy Lead as well as clinical study teams, data management (DM) team, Samples, Kits, Data, Logistics... ...samples transferred to internal research groups are documented, tracked,... ...Standards Complies with required training curriculum Completes timesheets accurately as...Suggested
$82k - $109k
Westat in Bethesda, Maryland is seeking a Lead Research Associate - Clinical Data Manager to develop, configure, and validate clinical research protocols. This hybrid role involves working on-site three days a week and requires a strong understanding of data management...3 days per week$43.4k - $108.2k
The Research Coordinator advocates for patient safety and protocol integrity, adheres to... ...effectively to ensure effective conduct of clinical trials and quality patient care.... ...to performing any study specific tasks Management of Clinical Trial Patients Collaborates...Full timePart timeImmediate startWorldwide$25 - $35 per hour
Job Title: Clinical Research Coordinator Hours: 30 hours per week (Monday-Friday) Contract duration: 3 months Job Description This part-... ...Clinical Research Coordinator role supports a cardiology study by managing study data and ensuring accurate documentation within the...Contract workTemporary workPart timeMonday to Friday- ...exceptional patient outcomes. This is an exciting opportunity for a clinical research professional eager to make a lasting impact in outpatient... ..., and communication skills Proficient with clinical trial management systems and electronic data capture tools Solid...
- Inova Fairfax Research Center - OBGYN team is seeking a dedicated Clinical Research Coordinator 1 to join the team. This role will be full-time day shift from... ...Clinical Practice (GCP), and non-GCP related study management activities. Minimum Qualifications: Experience:...Full timeRemote workMonday to FridayFlexible hoursDay shift
- A leading global clinical research provider is seeking a Research Coordinator in Arlington, Virginia. The role requires oversight of clinical... ...compliance. Essential duties include educating patients, managing trial activities, and ensuring accurate documentation. Candidates...
- A prominent healthcare organization in Falls Church is seeking a dedicated Clinical Research Coordinator 1 for a full-time day shift role. This position involves understanding the investigational products development process and performing study tasks under supervision....Full timeDay shift
$82k - $109k
29410BR Job Title: Lead Research Associate - Clinical Data Manager (Hybrid) Location: MD - Bethesda Job Description: Westat is a leader in research, data collection and analysis, technical assistance, evaluation, and communications. Our evidence-based...Full timeTemporary workH1bFlexible hours3 days per week- ...Inova Fairfax Hospital Campus is looking for a dedicated Clinical Research Nurse Coordinator 1 - Women's to join the team. This role will... ...with Good Clinical Practice (GCP) and non-GCP related study management activities. Explains the variety of communication channels...Full timeFlexible hours
$28.85 - $41 per hour
...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- ...trusted partner to federal health agencies and is seeking a Clinical Research Coordinator to support our clients within the Department of Veterans... ...well-being onation'stion's Veterans. You will coordinate and manage critical aspects of clinical studies, ensuring regulatory...Contract workFlexible hours
- **Seeking a Clinical Research Coordinator in Burlington, WA** Location : Burlington, Washingto nSchedule: Full time, onsite, 40 hrs a... ...esReview, resolve, and respond to data queri esCreate, manage, and maintain accurate source documentati onCoordinate monitor...Full time
$60k - $70k
...About the Position The Research Coordinator I oversees and administers research study and associated activities. Assists in project... ...research, education, training, and infrastructure for over 40 clinically relevant musculoskeletal injury (MSI) studies within the...Work experience placementInterim roleWork at officeFlexible hours- ...Senior Clinical Research Coordinator We are seeking a skilled Senior Clinical Research Coordinator (Sr. CRC) to support and oversee clinical... ...Unit (CRU) and centralized coordinator pool. This role manages complex studies from start-up through closeout, ensures compliance...Work experience placementWork at office
$44.02k - $73.41k
...University's mission of cura personalis. Clinical Trials offer a unique opportunity for a... ...weekly, or monthly, depending on the trial), management of the trials within the CRCII's... ...necessary, etc. The role of Clinical Research Coordinator II (CRCII) encompasses the management...Hourly payFull timeWork experience placementWork at office- ...Clinical Research Coordinator The Clinical Research Coordinator participates in or leads day-to-day operations of clinical research studies... ...or internship experience (e.g. research assistant, data manager, clinician or other interaction with a research population)....Full timeWork experience placementInternshipWork at officeShift workNight shift
$85k - $110k
...About the Position The Senior Clinical Research Coordinator (CRC) oversees and administers clinical research studies and associated... .... This position will assist with the development and management of study budgets. The Senior CRC will assist with the review...Work experience placementInterim roleWork at officeFlexible hours- ...We are seeking a skilled Senior Clinical Research Coordinator (Sr. CRC) to support and oversee clinical trials within a Clinical Research Unit (CRU) and centralized coordinator pool. This role manages complex studies from start-up through closeout, ensures compliance...Work experience placementWork at officeNight shift
- ...candidate is responsible for : Manages all operational aspects for implementation of one or more clinical trials and all activities... ...operational review and content to the study protocol and coordinates... ...with required training curriculum Completes timesheets accurately...Contract workRemote work
$125k - $138k
...Home Based (Preference for CA, CO, or TX locations) The Clinical Project Manager for Early Phase (EP) leads Parexel and Sponsor teams by leveraging clinical research experience and project management skills to develop tailored solutions for sponsors. This role requires...Contract workWork experience placementRemote workWork from home- A nonprofit organization advancing military medicine is seeking a Clinical Research Coordinator I for rehabilitation research. This entry-level role involves overseeing patient eligibility, collecting data, and coordinating research study logistics to support the ARMORR...
$86.5k - $216k
...Job Overview Manage a team of clinical staff working in support of clinical studies to ensure projects are appropriately resourced and employees... ...• Participate in the allocation of resources to clinical research projects by assigning staff to clinical studies based on...Full timePart timeLocal areaImmediate startWorldwide- ...Clinical Research Coordinator Live and work in a thriving urban center near the nation's capital. Bethesda, MD is located in southern... ...Collecting data obtained from research, coding and analyzing it Managing budgets set aside for research Communicating with...Local area
$90k - $105k
THE GENEVA FOUNDATION is seeking a Regulatory Affairs Manager to oversee regulatory compliance for the MIRROR Program. The role involves... ...boards, and ensuring adherence to regulatory standards for clinical research. This fully remote position supports projects across the...Remote job$60k - $70k
The Geneva Foundation is seeking a Research Coordinator I in Bethesda, Maryland. This role involves overseeing and administering research... ...multiple projects under the MIRROR program, contributing to clinically relevant studies within the military health system. Qualified...Flexible hours
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