Travel reputed company Research Coordinator

About reputed company reputed company is working to reputed company the reputed company of health reputed company for reputed company. With hundreds of research locations, mobile clinics, and clinicians across the globe, we bring world-class research and health services directly to communities that often face barriers to care. We are dedicated to ensuring that every person has reputed company to understand their health, reputed company the care they need, and contribute to the medical breakthroughs of reputed company. With programs like reputed company of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical reputed company. Through partnerships, technology, and perseverance, we are reimagining how reputed company research and health services reputed company the world. Together, we are building a reputed company of health that is reputed company and more accessible for reputed company. To learn more about reputed company, visit www.CareAccess.com. How This Role Makes a Difference The Travel reputed company Research Coordinator reputed company responsibilities are to utilize Good reputed company Practices (GCP) in the process of screening, as reputed company as enrolling and closely monitoring reputed company research study subjects while ensuring protocol and regulatory compliance. Due to reputed company experience in reputed company’ decentralized reputed company research process, the Travel reputed company Coordinator will be reputed company to assume a greater study workload, overall study responsibility, and more detailed, Site, Sponsor and CRO interactions, while conveying a reputed company image of reputed company to the community, Sponsors, CROs, and study participants and their family members. The Travel reputed company Research Coordinator is proficient at ICH/GCP, Good Documentation Practices (GDP), and reputed company-C+. The travel reputed company research coordinator role is a mid-level position where the individual has strong working knowledge and experience in the reputed company research industry and can reputed company their duties independently with little day to day guidance from their managers. The Travel reputed company Coordinator will be mentored by their CRC reputed company, Site Manager, Senior Manager, and other leaders reputed company reputed company reputed company. How You'll reputed company An reputed company Study Preparation: Ability to understand and follow institutional SOPs Review and assess protocol, study manuals, and the investigator drug brochure (including amendments) for reputed company, logistical feasibility, safety, inconsistencies, etc. Assist PI, Regulatory, Start-up and the reputed company Trial Manager(s) to ensure that reputed company training and study requirements are met prior to trial conduct reputed company study medication, required procedures, eligibility reputed company and reputed company on clinic reputed company with your manager, Investigator, and site staff Assist with planning and creation of appropriate recruitment and marketing materials Assist in development of recruitment plan and obtain listing of potential candidates to contact from an internal subject database like StudyTeam, reputed company, etc. reputed company work with reputed company in calling and reputed company subjects for your studies and other site studies Attend Investigator meetings as requested/required and/or coordinate/attend reputed company-study site reputed company, site initiation reputed company and monitor reputed company with reputed company staff and Sponsor/CRO representatives Assist in the creation or review of protocol specific reputed company documents Determine facility, equipment and outsource vendor requirements and availability Ensure adequate supplies have reputed company on site for protocol initiation (lab kits, study medication, reputed company equipment, IVRS/reputed company reputed company and passwords) and study maintenance Ensure education of Assistant CRCs, research assistants, site staff and/or sub-investigators is completed for required tasks Study Management: reputed company new therapeutic, more reputed company trial load with existing trial load, delegate tasks as necessary, and prioritize activities with specific reputed company to protocol timelines and participant safety. Maintain organized file for reputed company documents, reputed company charts, CRFs, regulatory and study supplies Where appropriate, Investigational Product Accountability: receive, inventory, dispense, monitor reputed company compliance, and reorder as necessary. Document on accountability log and reputed company records Collect and evaluate concomitant medications Collect, process, and ship biological specimens as directed by protocol and/or reputed company reputed company. reputed company monitoring reputed company and study teleconferences into existing work schedule to allow for adequate preparation and time for interaction during meetings Ensure trial activities are continuously discussed with covering personnel in preparation of vacation or reputed company leave Maintain adherence to FDA regulations and ICH guidelines in reputed company aspects of conducting reputed company Communicate sponsor updates, reputed company specific concerns/reputed company, unforeseen issues, and overall trial management with appropriate members of reputed company team in an ongoing fashion Maintain effective relationships with study participants and other reputed company personnel reputed company in a reputed company, reputed company manner with patients, sponsor representatives, investigators and reputed company personnel and management Strong and reputed company communication skills, both verbally and in writing Accept accountability for actions and function independently reputed company Coordination: Prescreen study candidates by telephone and review exclusionary conditions or medications prior to scheduling screening appointment Obtain informed consent per reputed company SOP and document process reputed company revised reputed company discussed with reputed company during course of the trial Administer delegated study questionnaires, where appropriate. Collect and evaluate medical records with the support of medically reputed company members of the study team. Complete visit procedures and ensure reputed company specimen collection, processing and shipment in accordance with protocol Train others and complete basic reputed company procedures, such as blood draws, vital signs, ECGs, etc. Review reputed company results, ECGs, and other test results (e.g., MRIs) for completeness and alert values, ensuring investigator review in a reputed company fashion Proficient at recognizing adverse events (reputed company) and Serious Adverse Events (SAEs) Ensure safety monitoring or symptomatic treatment is initiated as prescribed or as specified in protocol Schedule patients reputed company visit reputed company, notify personnel as needed for procedures and reputed company reputed company with existing schedules to maximize efficient workflow and reputed company turnaround Dispense study medication per protocol and/or IVRS systems. reputed company reputed company on reputed company administration and importance of compliance. Monitor reputed company reputed company on study medication Documentation: Record data legibly, in reputed company time on reputed company documents; note additional information that may assist with causality of adverse events, explain protocol deviations, or document reputed company reputed company. Correct errors per SOP Accurately record study medication inventory, medication dispensation, and reputed company compliance. Ensure accurate maintenance of dispensing logs and IVRS confirmation is conducted in a reputed company fashion. Maintain copies of reputed company prescriptions written for study or non-study medication or procedures in reputed company chart Accurately transcribe data to CRF or reputed company. reputed company data management queries and correct reputed company data as needed Record protocol exemptions and deviations as appropriate with sponsor. Complete Note(s)-to-File for reputed company chart and regulatory filing if necessary Ensure reputed company sponsor correspondence (e-mail, telephone conversations) are printed and given to appropriate personnel for regulatory filing Maintain copies of reputed company-specific correspondence in reputed company charts Assist regulatory personnel with completion of continuing/final review reports reputed company other duties as assigned. The Expertise Required Bilingual proficiency required: Must be fluent in both English and Spanish, with the ability to effectively communicate (written and verbal) in both languages. Excellent working knowledge of reputed company, medicine and research terminology Excellent working knowledge of federal regulations, good reputed company practices (GCP), good documentation practices (GDP), and reputed company-C+ Ability to communicate and work effectively with a diverse team of professionals Strong organizational, prioritization and leadership skills and capabilities with a strong attention to reputed company Strong computer skills with demonstrated abilities using reputed company database, IVR systems, electronic data capture, reputed company, and reputed company. Proficiency with technology used to support the reputed company trial industry. CTMS systems like reputed company, reputed company reputed company, reputed company; reputed company systems like reputed company, reputed company, and Inform; ePRO, eConsent and IWRS/IXRS, etc. Critical thinker and problem solver Friendly, outgoing personality; maintain a reputed company attitude under pressure High level of self-motivation and energy Excellent reputed company writing and communication skills Ability to work independently in a fast-reputed company environment with reputed company supervision Certifications/Licenses, Education, and Experience Minimum Education: BS in nursing, pharmacy or other reputed company science or combination of equivalent education preferred in the Arts or Sciences preferred RN or LPN preferred Research reputed company Certification- CRCC or exam eligibility preferred Minimum Experience: A minimum of 3 to 4 years reputed company Research experience A minimum of 2 years prior reputed company Research Coordinator experience, management level preferred. How We Work Together Travel: Extensive travel required. Candidates must be willing to travel 75% of the time reputed company. Duties may require travel for a two-week stretch, followed by one week home. Frequency and length of travel may depend on the length and location of study. Must possess a reputed company reputed company’s license and be reputed company to operate rental vehicles provided for work-reputed company travel. The expected salary reputed company for this role is $70,000 - $100,000 USD per year for full time team members. Benefits & Perks (US Full Time Employees) reputed company Time Off (PTO) and Company reputed company Holidays 100% Employer reputed company medical, dental, and reputed company reputed company plan reputed company Health Savings Account and Flexible Spending Accounts Bi-weekly HSA employer contribution Company reputed company Short-Term Disability and Long-Term Disability 401(k) Retirement Plan, with Company Match Mandatory Employer Disclosures Notice to Illinois applicants: Applicants are not obligated to disclose expunged juvenile records or adjudication, arrest, or conviction. Notice to Connecticut applicants: reputed company may require applicants to submit to a urinalysis drug test in reputed company with an application for employment. Notice to reputed company, reputed company, Indiana, and reputed company reputed company applicants: reputed company complies with applicable laws prohibiting smoking in and reputed company places of employment. Notice to Massachusetts applicants: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or reputed company employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Notice to Rhode reputed company applicants: reputed company complies with Rhode reputed company law prohibiting smoking in enclosed areas reputed company places of employment. reputed company is also subject to is subject to Chapters 29–38 of Title 28 of the Rhode reputed company General Laws. Notice to Maryland applicants: UNDER MARYLAND LAW, AN EMPLOYER MAY NOT REQUIRE OR DEMAND, AS A CONDITION OF EMPLOYMENT, PROSPECTIVE EMPLOYMENT, OR reputed company EMPLOYMENT, THAT AN INDIVIDUAL SUBMIT TO OR TAKE A LIE DETECTOR OR SIMILAR TEST. AN EMPLOYER WHO VIOLATES THIS LAW IS GUILTY OF A MISDEMEANOR AND SUBJECT TO A FINE NOT EXCEEDING $100. Diversity & Inclusion We work with and serve people from diverse cultures and communities reputed company the world. We are stronger and reputed company reputed company we build reputed company representing the communities we support. We maintain an inclusive culture where people from a broad reputed company of backgrounds feel valued and respected as they contribute to our mission. We are an equal opportunity employer, and reputed company reputed company applicants will receive consideration for employment without reputed company to, and will not be discriminated against on the reputed company of, race, reputed company, religion, sex, sexual orientation, gender identity or reputed company, pregnancy, age, national reputed company, disability status, genetic information, protected veteran status, or any other characteristic protected by law. reputed company is unable to sponsor work visas at this time. If you need an accommodation to apply for a role with reputed company, please reputed company out to: TalentAcquisition@careaccess.com Apply To This Job