Children's Hospital of Philadelphia

11 job(s) at Children's Hospital of Philadelphia

Children's Hospital of Philadelphia Philadelphia
Oct 05, 2021
Full time
This role is responsible for the coordination of assigned community and hospital resource navigation activities within the scope of the Food Pharmacy 2.0 (FP) and Medical Financial Partnership (MFP) programs. The Food Pharmacy and Medical Financial Partnership are programs under the Healthier Together program, an initiative to improve the health of children in West and Southwest Philadelphia by addressing housing, trauma, hunger, and poverty.   The role functions collaboratively with social workers, community health workers, case managers, health care providers and community partners in clinical and community settings. This individual will be a crucial part of a team dedicated to addressing the impacts of poverty and hunger on the health of children, their families, and their community. The role is an engaging and dynamic face of these initiatives in interactions with patients, families, community partners, and other stakeholders. They will actively advance the accomplishment of the respective FP and MFP missions through patient and partner engagement.   This role will be based out of two of CHOP’s West Philadelphia primary care offices, in a hybrid in-person and virtual capacity. They will be primarily responsible for completing duties relevant to each organization on assigned days but have flexibility to reallocate time depending on client volumes, scheduling, and other needs. Synergistic offering of services is encouraged.   This role will report to the Manager of the Food Pharmacy and Director of the Medical Financial Partnership. The role will have a dotted line relationship to the Office of Community Relations and the Department of Social Work. Job Responsibilities Patient Engagement Engage in standardized outreach to patient families to make them aware of services and enroll interested families into FP/MFP programming Follow up in a timely manner with MFP and FP clients to administer a food and financial insecurity-focused needs assessment and provide resources to address identified barriers. Escalate concerns that emerge during client interactions to extended team members (e.g., community health workers, social workers, intimate partner violence counselors) as indicated Work with families to develop a mutually agreed upon action plan to follow through on referrals and recommendations. Follow up with families at determined intervals to provide continued support and resources throughout program enrollment. Empower clients and facilitate transition from programming at determined intervals and after accomplishment of client goals, per program metrics Assist in message creation and development, including website content, fact sheets, correspondences, emails, lecture, social media posts and other formats. Evaluate, develop, market, and implement initiatives to promote programming.   Job Responsibilities (Continued) Partner Engagement Liaise with internal and external partners to identify appropriate programs for client referrals. Develop and maintain internal and external partnerships appropriate for client referrals. Attend key internal and external meetings and events. Some travel may be required.   Documentation Maintain organized, accurate, and timely documentation of client encounters in the Epic electronic health record, REDCap, and other tracking systems. Utilize tracking systems to ensure client outreach efforts are consistent with program guidelines. Work with data analyst to generate summaries of client engagement activities   Job Responsibilities (Continued) Work with patients in the clinical and community setting. Establish contact to increase awareness, information resources, support programs and services, and other related needs Attends key internal and external meetings and events.  Some travel may be required. Collaborates and responsible for maintaining an ongoing relationship between internal & external stakeholders Evaluates, develops, markets and implements collaborative initiatives for patient population to promote supportive care programming
Children's Hospital of Philadelphia Philadelphia
Oct 05, 2021
Full time
This position works to develop and implement strategic communication plans and messaging for the Center for Pediatric Clinical Effectiveness (CPCE). Under leadership supervision, and in collaboration with stakeholders and subject matter experts, this position independently deploys a variety of communication channels and stays abreast of new trends and advances in digital communications and CHOP’s communications capacities. This position will serve as a liaison between CPCE and CHOP and Research Institute public relations and marketing services. CPCE is a research center within the Children’s Hospital of Philadelphia (CHOP) Research Institute which is dedicated to discovering and sharing knowledge about best practices in pediatric care. Clinical effectiveness research seeks to answer the question “What works?” in healthcare. Learn more about CPCE at https://cpce.research.chop.edu/. In 2020, with the support of the CHOP Research Institute leadership, CPCE engaged external consultants to conduct a robust strategic plan to examine ways the Center can strengthen, connect, and increase its impact on pediatric clinical effectiveness, child health, and CHOP’s care delivery model. Enhanced communication and dissemination were identified as crucial for the translation of clinical research into practice, as well as achieving greater internal and external visibility of CPCE.   Job Responsibilities Provides project leadership and writing/editing expertise for content-driven communications projects (e.g., website development and optimization, creation of promotion strategies, and adaptation of technical documents into materials for consumer, stakeholder and media dissemination. Match promotional needs with appropriate outreach strategies and tactics (e.g., blogging, trending media stories, social media campaigns, and communicating with key promotional partners external to CHOP) Assemble and manage project teams, often from different departments at CHOP, through use of project management tools Builds strong relationships with internal and external partners Hires, supervises, trains and mentors staff, which may be a mixture of students, freelance support, and/or full time staff as needed. Ensures appropriate and consistent branding for Center/Department and Hospital-wide initiatives. Prepares and manages budgets under the Communications Manager’s purview and keeps stakeholders apprised. Other duties as assigned.
Children's Hospital of Philadelphia Philadelphia, PA
Jul 28, 2021
Full time
The Children’s Hospital of Philadelphia (CHOP) Research Institute is seeking research personnel with specialized training (i.e., minimum of MPH, MSc, or MS) in epidemiology and/or biostatistics to support clinical research in the area of pediatric oncology. Under the direction and guidance of the principal investigator (PI), they will assume a lead role, in providing analytic support and project coordination activities for research involving prospective data, electronic health records, large administrative and survey datasets. This role will have data management and quantitative data analysis responsibilities as well as project coordination responsibilities. Therefore, proficiency with R, SAS, and/or STATA biostatistical software is required, and 3+ years of prior experience in clinical research methods and design is preferred. The candidate will independently perform study coordination, data collection and management, and statistical analyses based on plans developed collaboratively with the research team. They will apply new epidemiologic and biostatistical techniques for ongoing projects, participate in the interpretation and reporting of study results, support the preparation of manuscripts for peer-reviewed journals, and contribute to the development of grant proposals for external funding. They will serve as a collaborative member of the group by supporting a variety of research initiatives and interacting with other researchers within the institution and at other institutions. About the PI: Dr. Kelly Getz is an Assistant Professor of Epidemiology and Pediatrics in the Perelman School of Medicine (PSOM) at the University of Pennsylvania and affiliated faculty in the Center of Pediatric Clinical Effectiveness Research and the Research Institute at CHOP. Dr. Getz's research is focused on the treatment and supportive care of children and young adults with cancer, and on understanding and balancing the associated therapeutic benefits and toxicity risks, with an emphasis in cardio-oncology. She develops and applies advanced epidemiologic methods in observational research studies that impact clinical practice. Her research aims to improve both clinical outcomes and quality of life, and addresses treatment and outcome disparities, for pediatric cancer patients across diagnoses, during treatment, and into survivorship. Dr. Getz is widely published in the fields of pediatric oncology and epidemiologic methods. Job Responsibilities Activity Management Oversee staff work and the coordination of projects. Manage participant flow, quality controls, eligibility assessments and reviews. Plan and direct activities, methods, and treatments. Collaborate internally to review, improve and promote processes and procedures. Manage related data collection, analysis, management and databases / system use. Ensure activity compliance with protocol and regulatory requirements. Activity Coordination and Support Coordinate compliance, documentation and submissions for regulatory agencies. Direct and maintain related documentation, records, and events. Assist with activities including assessments, enrollment and collection. Assist with researching to develop methodologies, instrumentation and procedures. Participate in department presentations and publications.
Children's Hospital of Philadelphia Philadelphia, PA
Jul 28, 2021
Full time
The Urinary Stone Disease Research Network (USDRN) is conducting the Prevention of Urinary Stones with Hydration (PUSH) trial to determine whether a multi-component program of behavioral interventions will reduce kidney stone recurrence over a 2-year period. The intervention incorporates financial incentives, structured problem solving, patient choice, and remote monitoring of fluid intake through a “smart” water bottle. Intervention participants may receive Structured Problem Solving (SPS) from a health coach. Pursuing Optimal Organisms in People with Stones (POOPS) is a case-control study that seeks to identify the perturbations in the gut and urinary microbiome among individuals with kidney stone disease. POOPS is being conducted at CHOP, Penn, and the University of British Columbia. The CRA II will help coordinate PUSH and POOPS activities at CHOP and the University of Pennsylvania, with the primary responsibility being PUSH activities. These activities include screening patients, providing participants with study materials, tracking and improving study data, and ascertaining study outcomes. The ideal candidate will possess: Previous engagement in clinical research involving study participants Strong communication skills with various types of patients High organizational skills Job Responsibilities Providing technical and clinical support in the conduct of clinical studies: Filing and office organization Patient/research participant scheduling Patient/research participant history Data collection Data entry Data management Laboratory procedures Follow-up care Order materials/supplies Schedule research meetings Research Study Compliance Adhere to an IRB approved protocols Comply with Institutional policies, SOPs and guidelines Comply with federal, state, and sponsor policies Also may be responsible for any of the following: Participate in the informed consent process for study subjects Document and report adverse events Maintain study source documents Submit basic IRB reports Complete case report forms (paper and electronic data capture)
Children's Hospital of Philadelphia Philadelphia, PA
Jul 28, 2021
Full time
The successful candidate will join the research team of Dr. David Weber in the Center for Bone Health (Division of Endocrinology and Diabetes) at The Children’s Hospital of Philadelphia. Dr. Weber’s research focuses on improving the clinical care of children with impaired bone health from genetic conditions or secondary to severe childhood disease. He is building a research team that will work on multiple bone health related projects including investigator initiated prospective observational studies in children with primary (such as osteogenesis imperfecta) and secondary osteoporosis (such as Duchenne muscular dystrophy or diabetes), industry sponsored observational and clinical trials in children with rare bone diseases, quality improvement projects within the Center for Bone Health, and epidemiologic studies utilizing local and multi-center clinical records databases. The ideal candidate will have a Master’s Degree in Public Health, Epidemiology, Biostatistics or a related field. Prior research experience and in patient-oriented research is required. The applicant is expected to work comfortably as part of a research team and will work on multiple research studies at any given time. The successful applicant should have strong communication, writing, organizational, and analytical skills. Job responsibilities will include participation in grant writing, protocol development, study implementation, subject recruitment, conduct of study visits, study management, budget management, data analysis, and potentially contribution to manuscript writing. Dr. Weber works closely with other physicians and researchers within the Center for Bone Health, Metabolism, Nutrition, and Physical Development Research Affinity Group, and The Center for Pediatric Clinical Effectiveness. The candidate will be integrated within these research networks which will allow for robust senior, peer, and near-peer mentoring  and provide opportunities for career advancement. Job Responsibilities Core responsibilities Adhere to an IRB approved protocol Participate in the informed consent process of study subjects Support the safety of clinical research patients/research participants Coordinate protocol related research procedures, study visits, and follow-up care Screen, recruit and enroll patients/research participants Maintain study source documents Report adverse events Understand good clinical practice (GCP) and regulatory compliance Educate subjects and family on protocol, study intervention, etc. Comply with Institutional policies, standard operating procedures (SOPs) and guidelines Must comply with federal, state, and sponsor policies Related responsibilities Manage essential regulatory documents Register study on ClinicalTrial.gov Complete case report forms (paper & electronic data capture) and address queries Submit documents to regulatory authorities (e.g. IRB, FDA, etc.) and/or review/monitoring boards (ie, DSMB, independent safety officer) Facilitate pre-study, site qualification, study initiation, and monitoring visit Facilitate study close out activities Coordinate research/project team meetings Collect, process and ship laboratory specimens Schedule subject visits and procedures Retain records/archive documents after study close out Also may be responsible for any of the following: Manage study finances including sponsor invoicing & resolving study subject billing issues Develop advertisement materials Act as liaison for research subject, investigator, IRB, sponsor, and healthcare professionals Document investigational product (drug/device) accountability Self-monitor and self-audit responsibilities Develop informed consent document Maintain Clinical Trial.gov  Develop Case Report Forms Assignments to include more complex studies
Children's Hospital of Philadelphia
May 28, 2021
Full time
Job Summary The successful candidate will join the research team of Dr. Jeffrey Gerber in the Pediatric IDEAS Research Group at Children’s Hospital of Philadelphia. The clinical research assistant’s primary responsibilities will be to assist in the execution of a randomized controlled study to evaluate the safety and efficacy of a SARS CoV-2 vaccine. Dr. Gerber’s research focuses on the epidemiology and outcomes of antimicrobial use in children with the goal of improving clinical outcomes while limiting the emergence of antimicrobial resistance. His approach benchmarks antimicrobial use across clinical settings to identify high-impact targets for improvement, followed by 1) comparative effectiveness studies for clinical scenarios where practice variability exists in the absence of evidence; 2) interventions to implement and disseminate evidence-based practice where prescribing guidelines do exist; and (3) qualitative assessments of the clinician, practice, or institution-level factors that might drive antimicrobial prescribing. The applicant is expected to work comfortably as part of a research team. The candidate will be a member of the Pediatric IDEAS Research Group, a collaborative group of investigators within the Center for Pediatric Clinical Effectiveness (CPCE) at CHOP. The mission of the Pediatric IDEAS Research Group is to perform rigorous clinical and translational research that generates evidence on the prevention and treatment of infections to inform best practices and improve the health of children, families, and communities. Job Responsibilities Providing technical and clinical support in the conduct of clinical studies: Filing and office organization Patient/research participant scheduling Patient/research participant history Data collection Data entry Data management Laboratory procedures Research Study Compliance Adhere to an IRB approved protocols Comply with Institutional policies, SOPs and guidelines Comply with federal, state, and sponsor policies May be called upon to: Consent subjects, with appropriate authorization and training. Document and Report adverse events Maintain study source documents Complete case report forms (paper and electronic data capture) Required Education: Associates Degree or active enrollment in a Bachelor’s Degree Program Preferred Education: Bachelor’s Degree in related field To apply, please submit a resume and cover letter to Shawn O'Connor,  oconnors1@chop.edu . 
Children's Hospital of Philadelphia LOC_COLKET-Colket Translational Research
May 28, 2021
Full time
Job Summary The Children’s Hospital of Philadelphia (CHOP) Research Institute is seeking research personnel with specialized training (i.e., minimum of MPH, MSc, or MS) in epidemiology and/or biostatistics to support clinical research in the area of pediatric oncology. Under the direction and guidance of the principal investigator (PI), they will assume a lead role, in providing analytic support and project coordination activities for research involving prospective data, electronic health records, large administrative and survey datasets. This role will have data management and quantitative data analysis responsibilities as well as project coordination responsibilities. Therefore, proficiency with R, SAS, and/or STATA biostatistical software is required, and 3+ years of prior experience in clinical research methods and design is preferred. The candidate will independently perform study coordination, data collection and management, and statistical analyses based on plans developed collaboratively with the research team. They will apply new epidemiologic and biostatistical techniques for ongoing projects, participate in the interpretation and reporting of study results, support the preparation of manuscripts for peer-reviewed journals, and contribute to the development of grant proposals for external funding. They will serve as a collaborative member of the group by supporting a variety of research initiatives and interacting with other researchers within the institution and at other institutions. About the PI: Dr. Kelly Getz is an Assistant Professor of Epidemiology and Pediatrics in the Perelman School of Medicine (PSOM) at the University of Pennsylvania and affiliated faculty in the Center of Pediatric Clinical Effectiveness Research and the Research Institute at CHOP. Dr. Getz's research is focused on the treatment and supportive care of children and young adults with cancer, and on understanding and balancing the associated therapeutic benefits and toxicity risks, with an emphasis in cardio-oncology. She develops and applies advanced epidemiologic methods in observational research studies that impact clinical practice. Her research aims to improve both clinical outcomes and quality of life, and addresses treatment and outcome disparities, for pediatric cancer patients across diagnoses, during treatment, and into survivorship. Dr. Getz is widely published in the fields of pediatric oncology and epidemiologic methods. Job Responsibilities: Independently applies logic to set up cohort based on data plan as provided. Manages and manipulates data. Conducts statistical programming using statistical software Learns and applies new statistical theory and techniques for ongoing projects or proposals. Conducts statistical analysis Supports the preparation of manuscripts for peer-reviewed journals. Performs other related duties as assigned or directed in order to meet the goals and objectives of the research group. Required Education and Experience Required Education: MS biostatistics, statistics, clinical epidemiology, health services research, economics or a related field Required Experience: At least one (1) year of relevant experience At least three (3) years of experience in base SAS, SAS/SQL, SAS/STAT, SAS/GRAPH and SAS MACROS To apply, please submit a resume and cover letter to Shawn O'Connors,  oconnors1@chop.edu . 
Children's Hospital of Philadelphia
May 28, 2021
Full time
Job Summary This is a full-time research coordinator position that will support Dr. Senbagam Virudachalam’s research projects at the Children’s Hospital of Philadelphia. Dr. Virudachalam is a primary care physician and her research focuses on food justice, advancing equity in diet quality and health outcomes for all children. The primary project involves working with food-insecure families to promote fruit and vegetable consumption through vouchers and a food literacy and cooking skills intervention. The goal of this pilot is to empower low-income families to achieve improved fruit and vegetable intake. The ideal candidate would have a Master’s Degree in Public Health, Nutrition, or related field and would be responsible for the coordination of all clinical research activities within the scope of Dr. Virudachalam’s clinical research protocols. These activities may include: • Confirmation of subject eligibility, completion of case report forms, data clarification and entry in REDCap, assisting participants with survey completion • Coordination of clinical research activities conducted within the CHOP healthcare network • Training and supervision of junior staff • Ongoing review of study procedures and management of participant flow • Maintaining regular communication with study participants • Planning and leading/facilitating virtual cooking sessions • Packaging and shipping urine collection supplies to participants; maintaining inventory • Coordination of the collection and acquisition of urine samples from participants • Abstracting and coding data • Initiating and maintaining communication with the principal investigator(s) and sponsor(s) on the status of active projects, patient care issues and protocol performance. Additional core responsibilities are listed below. Job Responsibilities Core responsibilities Adhere to an IRB approved protocol Participate in the informed consent process of study subjects Support the safety of clinical research patients/research participants Coordinate protocol related research procedures, study visits, and follow-up care Screen, recruit and enroll patients/research participants Maintain study source documents Report adverse events Understand good clinical practice (GCP) and regulatory compliance Educate subjects and family on protocol, study intervention, etc. Comply with Institutional policies, standard operating procedures (SOPs) and guidelines Must comply with federal, state, and sponsor policies Related responsibilities Manage essential regulatory documents Register study on ClinicalTrial.gov Complete case report forms (paper & electronic data capture) and address queries Submit documents to regulatory authorities (e.g. IRB, FDA, etc.) and/or review/monitoring boards (ie, DSMB, independent safety officer) Facilitate pre-study, site qualification, study initiation, and monitoring visit Facilitate study close out activities Coordinate research/project team meetings Collect, process and ship laboratory specimens Schedule subject visits and procedures Retain records/archive documents after study close out To apply, please submit a resume and cover letter to Shawn O'Connor,  oconnors1@chop.edu . 
Children's Hospital of Philadelphia
May 28, 2021
Full time
We are seeking a full-time (1.0 FTE) clinical research coordinator for a two-year position beginning July 1, 2021. The clinical research coordinator will assist with all aspects of a research project that aims to reduce disparities in the identification and treatment of sleep disordered breathing (SDB), a prevalent sleep concern that is associated with significant health risks and disproportionately impacts youth of racial/ethnic minority backgrounds. This research project (“Sleep in Primary and Specialty Care Services [Sleep PASS]: Enhancing Primary Care Specialty Care Integration, Collaboration, Patient Outcomes, and Health Equity”) is supported by a Department of Pediatrics Chair’s Initiative and will be conducted in partnership with The Possibilities Project, an effort to optimize and redesign pediatric primary care services. During this research study, the clinical research coordinator and the research team will: develop and meet regularly with an Advisory Board of key clinician, family, and administrative stakeholders; create a clinical pathway that includes social work support, a nurse navigator, and a community/family partner to assist with referrals from primary care to specialty care for SDB assessment and treatment; and conduct an evaluation of this clinical pathway in the CHOP primary care network. The clinical research coordinator responsibilities include: organizing, scheduling, and record-keeping for Advisory Board meetings; literature review for sleep navigation design; IRB protocol development and submission; REDCap database creation and management; and subject recruitment, consent, data collection, and data management for the pilot evaluation. Additional responsibilities include basic data analysis and preparation of manuscripts, grant submissions, and presentations based on the research project and its findings. Familiarity with REDCap, Qualtrics, or other electronic survey tools, experience with data analysis, and skills in using Excel, SPSS, or other statistical programs is desirable. The clinical research coordinator will join an interdisciplinary team that is led by Drs. Ariel A. Williamson, Alexander G. Fiks, and James Guevara, who are faculty members in CHOP’s Center for Pediatric Clinical Effectiveness. Job Responsibilities The coordinator is expected to perform all core responsibilities (as applicable): • Adhere to an IRB approved protocol • Participate in the informed consent process of study subjects • Support the safety of clinical research patients/research participants • Coordinate protocol related research procedures, study visits, and follow-up care • Screen, recruit and enroll patients/research participants • Maintain study source documents • Report adverse events • Understand good clinical practice (GCP) and regulatory compliance • Educate subjects and family on protocol, study intervention, etc. • Comply with Institutional policies, standard operating procedures (SOPs) and guidelines • Must comply with federal, state, and sponsor policies Also may be responsible for any of the following: • Manage essential regulatory documents • Register study on ClinicalTrial.gov • Complete case report forms (paper & electronic data capture) and address queries • Submit documents to regulatory authorities (e.g. IRB, FDA, etc.) and/or review/monitoring boards (ie, DSMB, independent safety officer) • Facilitate pre-study, site qualification, study initiation, and monitoring visits • Facilitate study close out activities • Coordinate research/project team meetings • Collect, process and ship laboratory specimens • Schedule subject visits and procedures • Retain records/archive documents after study close out Preferred Education: BA/BS in a related field Preferred Experience: 2+ year(s) relevant clinical research experience Additional Technical Requirements: Requires effective writing, organizational and communication skills, and ability to multitask; basic knowledge of Good Clinical Practices and the regulations necessary for the protection of human subjects and the conduct of clinical research; demonstration of consistent professional conduct and attention to detail; ability to work effectively on a team.
Children's Hospital of Philadelphia
May 28, 2021
Full time
Job Summary The successful candidate will join the research teams of Dr. Laura Vella and Dr. Brian Fisher in the Pediatric IDEAS Research Group at Children’s Hospital of Philadelphia. Dr. Vella’s research is translational and focuses on vaccine responses in settings of immune health and immune compromise. Dr. Fisher's research focuses on infections in children with immunocompromising conditions. The applicant is expected to work comfortably as part of a research team. The successful applicant should have strong writing, organizational, and analytical skills. A collaborative working style is required. The successful applicant will be responsible for leading specific projects. The candidate will be a member of the Pediatric IDEAS Research Group, a collaborative group of investigators within the Center for Pediatric Clinical Effectiveness (CPCE) at CHOP. The mission of the Pediatric IDEAS Research Group is to perform rigorous clinical and translational research that generates evidence on the prevention and treatment. Job Responsibilities Core responsibilities Adhere to an IRB approved protocol Participate in the informed consent process of study subjects Support the safety of clinical research patients/research participants Coordinate protocol related research procedures, study visits, and follow-up care Screen, recruit and enroll patients/research participants Maintain study source documents Report adverse events Understand good clinical practice (GCP) and regulatory compliance Educate subjects and family on protocol, study intervention, etc. Comply with Institutional policies, standard operating procedures (SOPs) and guidelines Must comply with federal, state, and sponsor policies Related responsibilities Manage essential regulatory documents Register study on ClinicalTrial.gov Complete case report forms (paper & electronic data capture) and address queries Submit documents to regulatory authorities (e.g. IRB, FDA, etc.) and/or review/monitoring boards (ie, DSMB, independent safety officer) Facilitate pre-study, site qualification, study initiation, and monitoring visit Facilitate study close out activities Coordinate research/project team meetings Collect, process and ship laboratory specimens Schedule subject visits and procedures Retain records/archive documents after study close out Required Education and Experience Required Education: Associates Degree or active enrollment in a Bachelor’s Degree Program Required Experience: Three (3) years of coordination related, clinical related or research related experience. Preferred Education, Experience & Cert/Lic Preferred Education: Bachelor’s Degree in related field Additional Technical Requirements Excellent verbal and written communications skills Excellent time management skills Ability to collaborate with stakeholders at all levels To apply, please submit a resume and cover letter to Shawn O'Connor,  oconnors1@chop.edu . 
Children's Hospital of Philadelphia
May 28, 2021
Full time
This is a full-time research assistant position that will support Dr. Senbagam Virudachalam’s research projects at the Children’s Hospital of Philadelphia. Dr. Virudachalam is a primary care physician and her research focuses on food justice, advancing equity in diet quality and health outcomes for all children. The primary project involves working with food-insecure families to promote fruit and vegetable consumption through vouchers and a food literacy and cooking skills intervention. The goal of this pilot is to empower low-income families to achieve improved fruit and vegetable intake. Providing technical and clinical support in the conduct of clinical studies: • Filing and office organization • Patient/research participant scheduling • Patient/research participant history • Data collection • Data entry • Data management • Laboratory procedures Research Study Compliance • Adhere to an IRB approved protocols • Comply with Institutional policies, SOPs and guidelines • Comply with federal, state, and sponsor policies May be called upon to: • Consent subjects, with appropriate authorization and training. • Document and Report adverse events • Maintain study source documents • Complete case report forms (paper and electronic data capture) Required Education: Associates Degree or active enrollment in a Bachelor’s Degree Program Required Experience: One (1) year of relevant clinical research experience. Preferred Education: Bachelor’s Degree in related field Additional Technical Requirements • Familiarity with IRB and human subject protection. • Able to perform tasks independently • Able to work accurately and pay strict attention to detail. • Able to work in collaboration with other professionals and staff. • Must have strong writing, organizational, and analytical skills.   To apply, please submit a resume and cover letter to Shawn O'Connor,  oconnors1@chop.edu .