13915 clinical research coordinator jobs found

Summary The Clinical Research Coordinator II is a Research Administration Office (RAO) team member responsible for assisting with the planning and implementation of clinical research studies. The CRC works closely with members of the research team to ensure protocol expectations are executed appropriately. Qualifications: Bachelor’s degree with 2 years of research experience or an equivalent combination of education and experience from which comparable knowledge and abilities can be acquired (i.e. a high school degree and 6 years of relevant research experience). Knowledge of medical terminology required. Knowledge of the principles of clinical research and federal regulations required. Competency in basic computer skills required - word processing, spread sheets. Excellent written, oral and team communication skills are essential. Attention to detail, organization, and self-motivation required. Licensure, Registration, and/or Certification:...

Summary The Clinical Research Coordinator (CRC) is a Research Administration Office (RAO) team member responsible for assisting with the planning and implementation of clinical research studies. The CRC works closely with members of the research team to ensure protocol expectations are executed appropriately. Qualifications: Bachelor’s degree with 0-1years of research experience or an equivalent combination of education and experience from which comparable knowledge and abilities can be acquired (i.e. HS degree and 4-5 years of relevant research experience). Knowledge of medical terminology required. Knowledge of the principles of clinical research and federal regulations required. Competency in basic computer skills required - word processing, spreadsheets. Excellent written, oral and team communication skills are essential. Attention to detail, organization, and self-motivation required. BLS required. PALS recommended. Additional...

Summary The Research Nurse Coordinator implements designated research trials and provides skilled clinical research nursing care to patients and families. Works closely with Principle Investigators to maintain high quality coordination of research through compliance with sponsor specific and regulatory guidelines. The Research Nurse Coordinator will deliver research nursing care to patients and families with a team-orientation, an emphasis on good customer relations, sound clinical judgment, and appropriate decision-making abilities that take into consideration evidenced based practice in line with the research protocol. Education & Experience Associates Degree plus RN required. Minimum 3 years of nursing experience required with 2 years research experience or an equivalent combination of education and experience from which comparable knowledge and abilities can be acquired (i.e. BSN and RN plus 3 years of nursing experience). Position requires an individual...

Abiomed is a pioneer and global leader in healthcare technology and innovation, with a mission of Recovering Hearts & Saving Lives . With corporate headquarters in Danvers, Massachusetts, and offices in Baltimore, MD, Woburn, MA, Aachen & Berlin, Germany and Tokyo, Japan, Abiomed's 2,000 employees form one of the fastest growing medical device companies in the world. We attract and retain exceptional talent with our collaborative culture, passion for our work, and a strong commitment to employee professional development. Patients First | Innovation | Winning Culture | Heart Recovery We are looking for a strong clinical scientist to support the development and design of Abiomed's global clinical studies with the focus on sound clinical evidence generation to drive better patient outcomes with the use of Abiomed products. The Senior/Clinical Research Scientist will provide scientific support for clinical studies within the Clinical and Regulatory Affairs...

Company DescriptionOur mission to find therapies for neurological and rare diseases is a unique focus within our industry and this shared purpose is what connects us as a team. We work together to overcome obstacles and to follow the science. We are resilient as we strive to make an impact on our patients' lives and on changing the course of medicine.Together, we pioneer. Together, we thrive.Job DescriptionAbout This Role The Real World Evidence Study Lead leads Study Management Teams (SMTs), provides clinical study management expertise and oversight for the execution of post- approval drug research. In this role, the successful candidate will act as the operational partner in driving data generation program planning and execution. Working across late-stage development and marketed products, the incumbent will drive operations for Phase 4 Observational studies, patient registries, outcomes research, and real-world evidence programs. Activities include study and program planning and...

Summary The Research Nurse Coordinator implements designated research trials and provides skilled clinical research nursing care to patients and families. Works closely with Principle Investigators to maintain high quality coordination of research through compliance with sponsor specific and regulatory guidelines. The Research Nurse Coordinator will deliver research nursing care to patients and families with a team-orientation, an emphasis on good customer relations, sound clinical judgment, and appropriate decision-making abilities that take into consideration evidenced based practice in line with the research protocol. Education & Experience Associates Degree plus RN required. Minimum 3 years of nursing experience required with 2 years research experience or an equivalent combination of education and experience from which comparable knowledge and abilities can be acquired (i.e. BSN and RN plus 3 years of nursing experience). Position requires an individual...

The primary function of this position is to provide project management support for Convergence projects. With oversight from project team leader or director, you will be responsible for managing multiple projects in the area. In addition to projects, this role will also have the responsibility of assisting in the operations activities as required. Responsibilities: Primary responsibility is to provide project management for 2-3 projects depending on complexity (agenda, minutes, action item follow up) Work with stakeholders to manage expectations for the projects. Stakeholders are cross functionals teams within Research and Development Collaborate with different partners (suppliers, procurement, etc) to align on any contractual agreements needed to support the respective projects and ensure agreements are executed via Abbvie processes Establish and maintain strong working relationships with all stakeholders Evaluate ways of working for the Convergence team...

Company: KARL STORZ Endoscopy-America, Inc. (KSEA) Job Code: 13272 Pay Grade: US-C11 Salary Range: $21.78 - $33.82 Description KARL STORZ SE & Co. KG based in Tuttlingen, Germany, is a family-owned, global company committed to benefiting humanity by advancing medical technology through innovation and education. For more than 75 years, KARL STORZ has been dedicated to earning its international reputation as a leader that designs, engineers, manufactures, and markets all its products with an emphasis on visionary design, precision craftsmanship, and clinical effectiveness. KARL STORZ is currently seeking a Credit and Collections Coordinator to join the Credit & Collections Department. As a Credit and Collections Coordinator, you will serve as a key member of the F&A team and will report to the Credit and Collections Supervisor. This position collects, manages and provides resolution of outstanding invoices from past due accounts. This person...

Summary Cook Children’s Health Care System (CCHSC) in Fort Worth, Texas, has a dynamic opportunity for a full-time board eligible/board certified Neonatologist. The successful candidate will have a passion for the NICU graduate/survivor population, and will be working in our NEST Developmental Follow-up Clinic. While developmental follow-up is our primary mission, we serve to address many of the social determinants of health that impact this population, and their developmental outcomes long-term. We view ourselves as a medical home for these families, and a resource to help them navigate the complexities of life after NICU discharge. Position Specifics: Performing standardized neurological assessments, as well as administration of validated developmental assessments and screeners. Working collaboratively with neurologists, developmental pediatrician, developmental psychologist, nurse coordinator, social workers, dietitians, parent liaison, medical assistants,...

Site Name: Upper Providence, RTP Posted Date: Feb 9 2023 Associate Director / Manager, Pharmacovigilance QA (Quality Assurance) Audit The purpose of this role is to provide PV Quality Assurance within GSK R&D, by (1) providing input into the development, management, and implementation of strategies and initiatives, policies and procedures to support the PV audit program across GSK R&D, (2) Identifying compliance issues, monitoring trends and (3) being accountable for driving quality improvements back into Global Safety and improve PVQA processes. The successful applicant will lead holistic QA activities by supporting the business, being involved in PV regulatory inspections and building solid working relationships with Global Safety stakeholders to build network of contacts while maintaining knowledge of local regulatory frameworks and global regulatory reporting requirements. In this role you will Assist in the development, management, and implementation of...

Site Name: UK - Hertfordshire - Stevenage, RTP, Upper Providence, Wavre Posted Date: Feb 9 2023 Associate Director / Manager, Pharmacovigilance QA (Quality Assurance) Audit The purpose of this role is to provide PV Quality Assurance within GSK R&D, by (1) providing input into the development, management, and implementation of strategies and initiatives, policies and procedures to support the PV audit program across GSK R&D, (2) Identifying compliance issues, monitoring trends and (3) being accountable for driving quality improvements back into Global Safety and improve PVQA processes. The successful applicant will lead holistic QA activities by supporting the business, being involved in PV regulatory inspections and building solid working relationships with Global Safety stakeholders to build network of contacts while maintaining knowledge of local regulatory frameworks and global regulatory reporting requirements. In this role you will Assist in the...

Site Name: Korea - Seoul Posted Date: Jan 11 2023 Why GSK? GSK is a global biopharma company with a special purpose - to unite science, technology and talent to get ahead of disease together - so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns - as anorganisationwhere people can thrive.Getting ahead means preventing disease as well as treating it, and we aim to impact the health of 2.5 billion people around the world in the next 10 years. Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves - feeling welcome, valued and included. Where they can keep growing and look after their wellbeing.So, if you share our ambition...

Site Name: Poznan Grunwaldzka, Warsaw Cirrus Posted Date: Jan 5 2023 GSK is a global biopharma company with a special purpose - to unite science, technology and talent to get ahead of disease together - so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns - as an organization where people can thrive. Getting ahead means preventing disease as well as treating it, and we aim to impact the health of 2.5 billion people around the world in the next 10 years. Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves - feeling welcome, valued and included. Where they can keep growing and look after their wellbeing.So, if you share our...

Site Name: Poznan Business Garden Pastelowa, Warsaw Posted Date: Nov 21 2022 GSK is a global biopharma company with a special purpose - to unite science, technology and talent to get ahead of disease together - so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns - as an organization where people can thrive. Getting ahead means preventing disease as well as treating it, and we aim to impact the health of 2.5 billion people around the world in the next 10 years. Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves - feeling welcome, valued and included. Where they can keep growing and look after their wellbeing.So, if you...

Job Description Westat is an employee-owned corporation providing research services to agencies of the U.S. Government, as well as businesses, foundations, and state and local governments. Westat's research, technical, and administrative staff of more than 2,000 is located at our headquarters in Rockville, Maryland, near Washington, DC. Westat is committed to building a diverse workforce and a culture of inclusivity, belonging and equity for all. We believe that our greatest strength draws on the different backgrounds, cultures, perspectives and experiences of our employees. Westat seeks a Lead Research Associate to contribute to nationally significant maternal and child health research funded by HRSA, CDC and NIH. In this role you will assist in managing the day-to-day activities of ongoing research projects involving project planning and implementation, protocol, and materials development, liaising with clinical sites and external investigators, and the collection,...

The Scientific Director oversees the direction, planning, execution, and interpretation of Medical Affairs initiatives for US Dermatology. Participates in cross-functional teams to generate, deliver, and interpret high-quality clinical data supporting overall product scientific and business strategy. Key responsibilities include: Provides scientific strategic and operational execution excellence of core medical affairs activities such as: building out training plan for new disease areas of focus, MSL decks, interactive medical aids and medical educational initiatives and Advisory boards. Support program governance and cross-functional teams, including interacting and coordinating appropriate scientific and medical activities with internal stakeholders (i.e., commercial, HEOR, clinical operations, discovery, statistics, regulatory, etc.) as they relate to medical affairs. Develops, reviews and follows up on clinical studies and medical projects initiated within the...

The Position The Field Implementation Specialist - WEST is an entry-level, national position that serves as the primary liaison representative providing post-sales customer support during the installation, implementation, training, and maintenance of clinical chemistry and immunoassay platforms and processes, such as cobas Pro and cobas 8000. As an entry-level specialist, you will be mentored to provide highly visible, self-supervised, self-directed, and extensive onsite advisory customer support. Some job duties may be performed remotely and independently following standard practices and procedures. Duties are generally routine but may include non-routine tasks. This is a field-based, national role. Ideal candidates should currently reside within 50 miles of a major metropolitan airport in the US in the following cities: Phoenix, AZ Salt Lake City, UT Los Angeles, CA San Diego, CA This position requires 95% travel to client sites. Due to our...

Jazz Pharmaceuticals plc (NASDAQ: JAZZ) is a global biopharmaceutical company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases - often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines and novel product candidates, from early- to late-stage development, in neuroscience and oncology. We actively explore new options for patients including novel compounds, small molecules and biologics, and through cannabinoid science and innovative delivery technologies. Jazz is headquartered in Dublin, Ireland and has employees around the globe, serving patients in nearly 75 countries. For more information, please visit www.jazzpharmaceuticals.com and follow @JazzPharma on Twitter. This Job Description provides a summary of the duties and/or characteristic of work performed and is not inclusive of every detail of the job for every...

Janssen/J&J is recruiting for a Senior Scientific Director, Pathobiology within the Preclinical Safety Translational Sciences organization. This position can be located in either Spring House, PA or Beerse, Belgium. The Senior Scientific Director of Pathobiology, Preclinical Safety Translational Sciences (PSTS) will work with other leaders in Preclinical Sciences and Translational Safety organization as well as interface with Therapeutic Area scientific leaders to provide strategic and scientific input to multidisciplinary Project Teams across the pipeline from discovery through post-registration and advise on regulatory readiness and interactions, as well as issue resolution. The incumbent is expected to have sufficient drug development experience to consult with senior leaders on the development of novel therapeutics spanning various therapeutic areas and modalities including small molecules, biologics, siRNA, gene therapy, vaccines, and other novel modalities. The...

MEDICAL SCIENTIFIC LIAISON Location: Gauteng Contract: Permanent The responsibilities & the impact YOU will have: Job Purpose: To be a therapeutic area scientific expert, responsible for discussing our products, patients' treatment trends and studies in the therapeutic areas in which we are involved, on a peer-to-peer basis with a defined audience of Leading Specialists (Physicians, Pharmacists, Hospital Managers, Board Members of Scientific Societies, and other stakeholders) and to be considered a trusted scientific counterpart and partner. To maximize company product value through high scientific quality communication with Leading Specialists on a peer-to-peer basis. Through activities in line with the Medical Affairs Plan, the MSL is jointly responsible for the realization of short-term and long-term company goals. The main duties and responsibilities of the position are: To keep abreast of medical and scientific knowledge....