Research Regulatory Assistant
Found in: Resume Library US A2 - 2 weeks ago
Retina Consultants of Texas (RCTX) is seeking an individual who is passionate about research and the regulatory field. The candidate will be primarily responsible for assisting in creation, completion, and maintenance of regulatory study start-up. This individual should be detailed oriented, have the ability to multi-task, and willing to learn. This position will be based from our Bellaire/Newcastle clinic.
Candidate must be able to work shift anytime between 6:30 am -5 pm, Monday-Friday. Schedules are provided by your leader and can be discussed further during the interview process.
RCTX offers the following competitive benefits for full-time eligible employees after the introductory period:
Medical Insurance Plans
Vision Insurance Plan
Dental Insurance Plan
401K Contribution
Life Insurance
PTO and Vacation Pay
Rewards and Recognition Program
Certification Opportunities
Retina Consultants of Texas (RCTX) is one of the largest and most respected retina-only ophthalmology practices in the United States, committed to Preserving the Patient's Vision. RCTX has three certified research centers and is home to the Greater Houston Retina Research Center, one of the country’s leading sites for retinal research. All Retina Consultants of Texas physicians are board certified by the American Board of Ophthalmology and specialize exclusively in diseases and surgery of the retina, vitreous, and macula. In addition, RCTX has an ocular oncology division, which focuses on cancer treatments for the eye. Our surgeons have studied at some of the most renowned institutions in the nation and all have graduated at the very top of their classes.
Retina Consultants of Texas (RCTX) is part of Retina Consultants of America (RCA), the largest network of leading retina specialists with the mission of saving sight and improving patient lives through innovation and the highest quality care. Through RCA's physician-centered practice management model, physicians continue to drive clinical and practice culture while benefiting from the available business expertise, resources and shared best practices.
Retina Consultants of Texas follows all CDC and local authority protocols to ensure the safety and well-being of the patients, providers, employees and communities.
Retina Consultants of Texas is proud to be an Equal Employment Opportunity and an Affirmative Action Employer. We are committed to creating an inclusive work environment that celebrates diversity.
Responsibilities:
Duties and Responsibilities:
Compiles and prepares materials for submission to regulatory agencies
Reviews clinical protocols to ensure collection of data needed for regulatory submissions
Identifies relevant guidance documents
Occasional travel to other Retina Consultants of America Research clinics for regulatory support
Assists in communicating study requirements to all individuals involved in the study
Assists with creation and distribution study documentation to the internal RCTX Research study team in accordance with sponsor requirements and RCTX Research policies and procedures including, but not limited to, study protocols, financial disclosure forms, FDA 1572 forms, study site logs and other essential documents.
Assists with completion of study documentation of study files to the Sponsor and/or CRO in accordance with sponsor requirements and RCTX Research policies and procedures including, but not limited to, study protocols, financial disclosure forms, FDA 1572 forms, study site logs and other essential documents.
Assists with maintaining electronic files in Clinical Trial Management System (RealTime) and any other sponsor portals where electronic files may be kept (i.e., Medpace, PPD, Activate/GoBalto, VeevaVault, DrugDev, CLIX, etc.).
Continuously updates the internal study progress tracker.
Assists with maintaining effective and ongoing communication with sponsor, research team, Directors, and PI during the course of the study.
Assists with ensuring protection of the rights and welfare of all human research participants involved in research in accordance with Federal regulations.
Other duties as assigned
Qualifications:
Skills/Competencies:
Knowledge regarding GCP, FDA
Knowledge of medical terminology and clinical research
Takes initiative
Goal-driven mindset
Strong customer service skills
Strong analytical and problem-solving skills
Excellent organizational skills, detail oriented, efficient, and able to multi-task and prioritize effectively
Excellent interpersonal skills· Strong written and verbal communication skills
Ability to competently use Microsoft Office, including Word, PowerPoint, Excel, TEAMS, (url removed) and appropriate practice management software.
Education Requirements:
Bachelor’s Degree and/or 2+ years’ experience in Research in lieu of degree
Experience Requirements:
Applicant must have “hands-on” research experience and working knowledge of FDA regulations, OHRP regulations, ICH and GCP guidelines, and document review.
Physical Demands:
Must be able to sit for long periods of time
Must be able to write
Must be able to communicate via telephone and email
Must be able to read medical charts
-
Research Regulatory Assistant
1 week ago
Houston, United States Retina Consultants Of Texas Full timeOverview: Retina Consultants of Texas (RCTX) is seeking an individual who is passionate about research and the regulatory field. The candidate will be primarily responsible for assisting in creation, completion, and maintenance of regulatory study start-up. This individual should be detailed oriented, have the ability to multi-task, and willing to learn....
-
Research Assistant
1 day ago
Houston, United States EVOLUTION RESEARCH GROUP Full timeJob DetailsJob LocationLOC010 HDR Memorial Hermann Village inc HHH - Houston, TXResearch Assistant (PRN)Title: Research Assistant Location: Houston, TXAbout us:ERG is a leading U.S. based, privately held, independent clinical research site company, and provider of clinical development services with expertise in early and late-stage neuroscience drug...
-
Research Assistant
1 day ago
Houston, United States EVOLUTION RESEARCH GROUP Full timeJob DetailsJob LocationLOC010 HDR Memorial Hermann Village inc HHH - Houston, TXResearch Assistant- NIGHTSTitle: Research Assistant, PRN NightsLocation: Houston, TXAbout us:ERG is a leading U.S. based, privately held, independent clinical research site company, and provider of clinical development services with expertise in early and late-stage neuroscience...
-
Clinical Research Assistant
1 week ago
Houston, United States SCLA Management Full time**Overview**: As a Clinical Research Administrative Assistant, you will play a key role in providing administrative support to our research team and ensuring the smooth operation of clinical trials and research studies. You will work closely with research coordinators, operations, regulatory, investigators, and study participants to facilitate the execution...
-
Regulatory Accountant
2 weeks ago
Houston, United States The Burchell Group Inc. Full timeJob DescriptionJob DescriptionJob Title: Regulatory AccountantType: Direct Hire Location: Houston, TX - HybridExperience: 3 years Our client in Downtown Houston is looking for a Regulatory Accountant to partner with Regulatory, Land, and Revenue teams to research, prepare and file necessary regulatory accounting filings. This position will report to the...
-
Regulatory Specialist
6 hours ago
Houston, United States SageTech Resources Full timeOur client is seeking an experienced Regulatory Specialist who will encompass overseeing regulatory and technical matters pertinent to offshore shallow-water oil and gas production endeavors. This position involves meticulous document preparation and addressing regulatory challenges. Key Responsibilities: Preparing regulatory documentation essential for...
-
Regulatory Specialist
Found in: Appcast Linkedin GBL C2 - 1 day ago
Houston, United States SageTech Resources Full timeOur client is seeking an experienced Regulatory Specialist who will encompass overseeing regulatory and technical matters pertinent to offshore shallow-water oil and gas production endeavors. This position involves meticulous document preparation and addressing regulatory challenges.Key Responsibilities:Preparing regulatory documentation essential for...
-
Regulatory Specialist
Found in: Appcast US C2 - 1 day ago
Houston, United States SageTech Resources Full timeOur client is seeking an experienced Regulatory Specialist who will encompass overseeing regulatory and technical matters pertinent to offshore shallow-water oil and gas production endeavors. This position involves meticulous document preparation and addressing regulatory challenges.Key Responsibilities:Preparing regulatory documentation essential for...
-
HSE Environmental
Found in: beBee S US - 2 weeks ago
Houston, Texas, United States Petroplan Full timePetroplan is seeking an HSE Enviornmental & Regulatory Supervisor to join an industry-leading independent oil and natural gas exploration and production company local to Texas. Job Summary The Environmental and Regulatory Supervisor oversees compliance efforts for our clients operations in the US Onshore-Eagle Ford Shale (EFS) region, ensuring adherence...
-
Senior Coordinator, Regulatory Affairs
Found in: beBee S US - 3 weeks ago
Houston, United States Baylor College of Medicine Full timetendersglobal.net Summary This role provides administrative support functions to the Office of Clinical Research Initiatives, coordinates office communications and correspondence; creates and maintains regulatory documentation systems.This role will primarily be responsible for the daily administrative functions of the Office of Clinical Research...
-
Senior Coordinator, Regulatory Affairs
Found in: beBee jobs US - 2 weeks ago
Houston, Texas, United States Baylor College of Medicine Full timeSummaryThis role provides administrative support functions to the Office of Clinical Research Initiatives, coordinates office communications and correspondence; creates and maintains regulatory documentation systems.This role will primarily be responsible for the daily administrative functions of the Office of Clinical Research Initiatives and oversee...
-
Senior Regulatory Affairs Associate
Found in: beBee jobs US - 3 weeks ago
Houston, Texas, United States Baylor College of Medicine Full timeSummaryThis role will primarily be responsible for the overall implementation and management of clinical studies that are regulated under the European Union General Data Protection Regulation or GDPR, and specifically, how GDPR information must be provided to research subjects, including privacy notices and consent forms, as well as managing studies under...
-
Houston, United States P.O.&G. Resources, LP Full timePO&G Resources is a rapidly growing, twenty-three-year-old private oil and gas company located in the Galleria/Uptown area of Houston, TX. With the ongoing expansion of our operations across multiple areas in the US and the launch of a second investor fund, the company is seeking a key individual to fill the position of Regulatory Compliance and Production...
-
Regulatory Compliance and Production Assistant
Found in: Appcast Linkedin GBL C2 - 3 weeks ago
Houston, United States PO&G Resources, LP Full timePO&G Resources is a rapidly growing, twenty-three-year-old private oil and gas company located in the Galleria/Uptown area of Houston, TX. With the ongoing expansion of our operations across multiple areas in the US and the launch of a second investor fund, the company is seeking a key individual to fill the position of Regulatory Compliance and Production...
-
Regulatory Compliance and Production Assistant
2 weeks ago
Houston, United States PO&G Resources, LP Full timePO&G Resources is a rapidly growing, twenty-three-year-old private oil and gas company located in the Galleria/Uptown area of Houston, TX. With the ongoing expansion of our operations across multiple areas in the US and the launch of a second investor fund, the company is seeking a key individual to fill the position of Regulatory Compliance and Production...
-
Senior Regulatory Affairs Associate
Found in: beBee S US - 3 weeks ago
Houston, United States Baylor College of Medicine Full timetendersglobal.net Summary This role will primarily be responsible for the overall implementation and management of clinical studies that are regulated under the European Union General Data Protection Regulation or GDPR, and specifically, how GDPR information must be provided to research subjects, including privacy notices and consent forms, as well as...
-
Senior Regulatory Compliance Specialist
1 week ago
Houston, United States CareerBuilder Full timeAt Houston Methodist, the Senior (Sr.) Regulatory Compliance Specialist position is responsible for leading, coordinating and performing study specific regulatory processes such as local IRB submissions in compliance with Good Clinical Practices (GCP) and all local, state, and federal laws, regulations, guidance, policy and procedure developed by Houston...
-
Research Assistant
2 days ago
Houston, United States The Prelude Network Full timeThe Research Assistant is responsible for gathering accurate, credible data on every research participant and summarizing their findings to support senior team members' research. The duties include browsing archives for information, completing literature reviews and conducting research interviews. Specifically, to coordinate and conduct all data collection...
-
Regulatory Compliance Analyst
Found in: Resume Library US A2 - 3 weeks ago
Irving, Texas, United States 7-Eleven, Inc. Full timeOverview: ▶ Who we are Imagine working in a place where continuous improvement and innovation is celebrated and rewarded; where fast-paced, high-impact teams come together to positively drive results for one of the largest & most iconic brands in the world. As the only rapidly growing retailer, you may know us as your friendly neighborhood store. You...
-
Research Assistant
1 day ago
Houston, United States Prelude Fertility Full timeThe Research Assistant is responsible for gathering accurate, credible data on every research participant and summarizing their findings to support senior team members' research. The duties include browsing archives for information, completing literature reviews and conducting research interviews. Specifically, to coordinate and conduct all data collection...