Unfortunately, this job posting is expired.
Don't worry, we can still help! Below, please find related information to help you with your job search.
Some similar recruitments
Clinical Coordinator Jobs
Recruited by The US Oncology Network 9 months ago Address Germantown, KY, United States

Clinical Research Manager (Hybrid)

Company

Elligo Health Research

Address Paducah, KY, United States
Employment type FULL_TIME
Salary
Category Transportation, Logistics, Supply Chain and Storage
Expires 2023-06-02
Posted at 1 year ago
Job Description
Elligo Health Research is partnering with Aledade to find qualified candidates.


Aledade is a leader in population health that is using innovative, value based solutions to transform the way physicians interact with their patients. We are on a mission to change healthcare for the better and solve complex problems within the healthcare system.


We are growing the team with this newly created opportunity and searching for a dedicated and experienced Clinical Research Manager to join the team. This manager will be responsible for the daily and long-term operations of several clinical trials from start up through study close-out in the Kentucky Accountable Care Organization (ACO).


The Clinical Research Manager will help design, implement and refine a new model for delivering clinical research as part of care in primary care practices. In this role, the Clinical Research Manager will lead the way for providing everyone with easy access to clinical research as care to improve clinical quality, reduce disparities in research, increase patient access to new treatments, and support physicians in research participation.


Candidates must be located near Paducah, Kentucky. Regular local travel is required for this position.


Responsibilities


  • Manage multiple concurrent trials
  • Comply with Aledade, Clinic, Sponsor, and partner policies, standard operating procedures (SOPs) and guidelines
  • Collect and provide all documents required for research-related regulatory purposes
  • Assist with the screening, recruiting and enrollment of research subjects
  • Collect and maintains source documentation
  • Serve as the primary contact for clinical trials across the ACO to ensure appropriate communications, trial management, and meeting of timelines
  • Coordinate and conduct the informed consent process
  • Work closely with Aledade, practice leadership, and other partners to refine clinical trial approaches and identify strategies to bring clinical research as part of care to other Aledade markets
  • Ensure all research-required equipment is appropriately calibrated
  • Coordinate protocol related research procedures, study visits, and follow-up
  • Perform data entry and query resolution
  • Working closely with partners on all areas of clinical trials including start-up, vendor management, subject recruitment, protocol training, data entry, and reporting in compliance with sponsor requirements
  • Develop strong working relationships and maintain effective communication with study team members and key stakeholders
  • Maintain all trial-related training records as required
  • Adhere to an IRB approved protocol
  • Facilitate pre-study, site qualification, study initiation, monitoring visits, and study close out activities
  • Complete all protocol related training
  • Order supportive study supplies (e.g., contracts, IXRS, lab kits, nonclinical supply materials, imaging and laboratory handling manuals, etc.)
  • Other duties as assigned
  • Perform patient/research participant scheduling
  • Collect patient/research participant history
  • Communicate with internal teams, investigators, ACO board, and stakeholders
  • Support the collection and review of required essential study documents and reports
  • Support the safety of research subjects, report adverse events
  • Collect, process and ship laboratory specimens
Qualifications


  • Extensive knowledge of clinical research studies, protocols, etc.
  • BS/BA in Life Sciences or related discipline
  • Thinks beyond their immediate team and contributes to making Aledade holistically better (active engagement in D&I efforts, culture initiatives, facilitating training, leading roundtables, etc.)
  • 5+ years of clinical research coordinator experience
  • Exceptional interpersonal skills, the ability to work independently
  • Previous GCP training and certification
  • Self starter with the ability to run with things
  • Demonstrated proficiency with word processing, spreadsheet, database, and presentation software
  • Strong verbal and written communication skills
  • Ability to travel for clinical activities, attend investigator meetings or vendor visits/audits, as required
  • Demonstrated ability to build strong teams and relationships
  • Preferred: Nursing experience in a clinical setting
  • Strong organizational/prioritization skills for the management of multiple concurrent projects
All prospective hires will be required to demonstrate that they have been fully vaccinated, including booster shots, against COVID-19 with a COVID-19 vaccine for which the U.S. Food and Drug Administration has issued a license or an Emergency Use Authorization prior to mutually agreed upon start date at Aledade, unless they qualify for a medical or religious accommodation to this vaccination requirement.


If you are passionate about transforming the healthcare system into one that works better for patients, practices and society, we’d love for you to join us!


Who We Are:


Aledade, a public benefit corporation, exists to empower the most transformational part of our health care landscape - independent primary care.We were founded in 2014, and since then, we've become the largest network of independent primary care in the country - helping practices, health centers and clinics deliver better care to their patients and thrive in value-based care. Additionally, by creating value-based contracts across a wide variety of payers, we aim to flip the script on the traditional fee-for-service model. Our work strengthens continuity of care, aligns incentives, and ensures primary care physicians are paid for what they do best - keeping patients healthy.If you want to help create a health care system that is good for patients, good for practices and good for society - and if you're eager to join a collaborative, inclusive and remote-first culture - you've come to the right place.


What Does This Mean for You?


At Aledade, you will be part of a creative culture that is driven by a passion for tackling complex issues with respect, open-mindedness and a desire to learn. You will collaborate with team members who bring a wide range of experiences, interests, backgrounds, beliefs and achievements to their work - and who are all united by a shared passion for public health and a commitment to the Aledade mission.


In addition to time off to support work-life balance and enjoyment, we offer the following comprehensive benefits package designed for the overall well-being of our team members:


Flexible work schedules and the ability to work remotely are available for many roles


Health, dental and vision insurance paid up to 80% for employees, dependents, and domestic partners Robust time off plan 21 days of PTO in your first year 2 Paid Volunteer Days & 11 paid holidays


12 weeks paid Parental Leave for all new parents


6 weeks paid sabbatical after 6 years of service


Educational Assistant Program & Clinical Employee Reimbursement Program


401(K) with up to 4% match


Stock options


And much more!


At Aledade, we don’t just accept differences, we celebrate them! We strive to attract, develop, and retain highly qualified individuals representing the diverse communities where we live and work. Aledade is committed to creating a diverse environment and is proud to be an equal opportunity employer. Employment policies and decisions at Aledade are based on merit, qualifications, performance, and business needs. All qualified candidates will receive consideration for employment without regard to age, race, color, national origin, gender (including pregnancy, childbirth or medical conditions related to pregnancy or childbirth), gender identity or expression, religion, physical or mental disability, medical condition, legally protected genetic information, marital status, veteran status, or sexual orientation.


WORKING CONDITIONS


This job operates in a professional office environment. This role routinely uses standard office equipment such as computers, phones, and photocopiers.


Some flexibility in hours is allowed, but the employee must be available during the “core” work hours of 9:30 a.m. to 3:30 p.m. and must work a minimum of 37.5 hours each week to maintain full-time status. Occasional evening and weekend work may be required as job duties demand.


The above statements are intended to describe the general nature and level of work being performed by individuals assigned to this position. They are not intended to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel. More in-depth information can be found in SOP's, working guidelines, policies, etc.


Elligo is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at Elligo are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, national, social or ethnic origin, sex (including pregnancy), age, physical, mental or sensory disability, HIV Status, sexual orientation, gender identity and/or expression, marital, civil union or domestic partnership status, past or present military service, family medical history or genetic information, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. Elligo will not tolerate discrimination or harassment based on any of these characteristics. In addition, Elligo will provide reasonable accommodations for qualified individuals with disabilities.