Full Time
Farmington Hills, MI, Michigan, Southfield, MI, Troy
Posted 3 years ago
Unique opportunity to make an Impact in the healthcare industry…
IMPROVE THE FUTURE AS OUR CLINICAL RESEARCH COORDINATOR!
The professional we select for Revival Research Institute will have an overall responsibility to enhance our operational efficiency, market presence, affiliated partnerships, and staff development/performance.
The qualified candidate we are looking for should be genuinely respectful of diverse points-of-view and strive for an environment in which inclusiveness drives productivity and results.
Other requirements include:
- Bachelor’s degree with a Masters in a science-related field highly desired, or extensive experience in Clinical Research
- 2+ years of increasingly responsible management experience in the healthcare sector that includes strategy development, positive retention results, and creative problem-solving
- Strong analytical skills with the ability to assess current operational effectiveness and needs
- Engaging verbal/written communication skills and ability to comfortably interact with people from all kinds of backgrounds
- Powerful professional interpersonal skills with the ability to establish/nurture connections
- Successful background in healthcare and/or clinical research
- Proven ability to coach and motivate team members to reach new levels of accomplishment and professional fulfillment
- Must possess proficiency with modern technology
- Availability for some travel (domestic)
- Oversight of clinical trials
- Collection of data and timely entry
- Communicate with the study monitor
- Informing participants about study objectives
- Administering questionnaires as needed per study
- Monitor participants to ensure adherence to study rules
- Follow GCP guidelines and other regulatory standards
- Participate in subject recruitment efforts
- Obtaining informed consent of participants
Along with competitive base salary, there is potential for performance-based rewards. Committed to work/life balance, Revival Research Institute, LLC is invested in our staffs personal development and offer a number of opportunities for growth. If this position is of interest to you, we here at Revival Research would love to see your resume.
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Job Features
| Job Category | Clinical Research |
Unique opportunity to make an Impact in the healthcare industry… IMPROVE THE FUTURE AS OUR CLINICAL RESEARCH COORDINATOR! The professional we select for Revival Research Institute will have an overa...
Full Time
Southfield, MI
Posted 3 years ago
Join our community
Revive Research Institute has an excellent opportunity available within our Clinical Research Department as a Research Regulatory Coordinator. If you are looking for challenging work and meaningful advancement, then you should consider a career with Revive Research Institute.
Where you fit in
The Research Regulatory Coordinator leads, coordinates and oversees regulatory processes across multiple studies of different therapeutic areas and phases, in accordance with appropriate regulations, institutional policies, Standard Operating Procedures (SOPs), and study specific protocols/plans and processes independently. Studies may be large, nationwide, or moderately complex involving multiple sites and/or assessments/interventions.
Duties:
- Manages regulatory activities for all stages of clinical trials for assigned department (s). Prepares and submits regulatory documents to Sponsor and IRB and works with clinical research team to ensure submission documents are up-to-date.
- Maintains a working knowledge of all federal, state, and institutional guidelines regarding clinical trials. Provides guidance and training to research staff to ensure compliance with rules and regulations associated with clinical research studies.
- Completes industry registrations and study feasibility questionnaires including receipt, tracking and correspondence with Sponsor/CRO/ARO
- Prepare and submit start-up regulatory packets to Sponsor and IRB
- Oversee study start-up activities to including reporting and communicating with stakeholders on a regular basis
- Serve as a liaison to Sponsors/CRO/IRB/Investigators assuring continuity of service and problem resolution
- Monitor approval status of open studies by completing timely reviews
- Maintain master files of all regulatory-related documents
- Assist in submission of Investigational New Drug (IND) applications including amendments and reporting
- Coordinate schedules of on-site visits including introductions, tours, EMR access and Sponsor/CRO/ARO requests, and monitoring visits
- Associate Degree/Bachelor's Degree: Bachelor’s or Associate degree in a related field. An applicable degree may be nursing, life sciences, business administration, or health care administration or research administration. (Required)
- 1-2 years: Minimum of one (1) yeas of clinical research experience required. Prior regulatory experience preferred.
- Ability to be detail oriented
- Ability to be organized
- Ability to perform basic computer functions
- Ability to use customer service skills to provide an exceptional experience
- Ability to work effectively within a team environment
- Must be able to prioritize tasks; work well under stress, meet aggressive timelines, and problem solve to quickly and tactfully manage
- challenging situations concerning customer groups
- Must be willing to work flexible hours if needed
- Must demonstrate intermediate competency in the use of the Internet and the following Microsoft applications: Word, Excel, Outlook
- Personal Characteristics
- Ability to communicate effectively both orally and in writing
Job Features
| Job Category | Clinical Research |
Join our community Revive Research Institute has an excellent opportunity available within our Clinical Research Department as a Research Regulatory Coordinator. If you are looking for challenging wor...
The Clinical Research Medical Assistant, under the guidance and supervision of the Clinical Research Coordinator and Principal Investigator (PI), ensures the integrity and quality of clinical trials are maintained and conducted in accordance w/ federal, state, and local regulations, Institutional Review Board (IRB) approvals, and other policies, and procedures. This position is primarily responsible for the accurate completion of visit procedures and collection of information for study patients according to protocols, and for protecting the health, safety, and welfare of research participants.
Essential Functions:
- Lab Processing, handling & shipping
- Ensuring compliance with research protocols by reviewing all protocol requirements to confirm implementation of appropriate methods, practices, and procedures for all clinical
- Participating in recruitment and selection of study participants by interviewing and documenting medical history to determine compliance with eligibility
- Performing Clinical assessments including, but not limited to, vital sign EKGs & Venipuncture.
- Administering study medications and performing patient assessment during study visits to determine presence of side effects to medication; notifies principal investigator of findings/issues.
- Providing patient education and medical information to study patients to ensure understanding of proper medication dosage, administration, and disease
- Documenting medical data in subject chart to ensure availability of timely records for decision
- Phlebotomy Experience REQUIRED
- Valid MA license from the State of Texas (Preferred)
- Minimum of a high school diploma required
- Two (2) years of recent clinical experience in a hospital, clinic, or similar health care setting. (Preferred)
- One (1) year clinical research experience (Preferred)
- Must be proficient in Microsoft Office Word and Excel, electronic health systems and databases used in research environment, or willingness to learn and demonstrate proficiency within three months of hire
- Effective written, verbal, and interpersonal communication
- Excellent attention to detail
- Ability to manage multiple tasks w/ time deadlines.
- Ability to be flexible, organized, detail oriented and tenacious in follow-through.
- Possess the ability to work well under pressure
- Prioritization and organizational
- Proficient in medical terminology
- Problem-solving mindset
- Clinical competency skills per scope of practice (i.e., performing vital signs, clinical assessments, performing ECG/EKG, giving injections, etc.)
- Knowledge of GCP, federal, state, and local regulations, including HIPAA policies
- CPR-certification preferred
Job Features
| Job Category | Clinical Research |
The Clinical Research Medical Assistant, under the guidance and supervision of the Clinical Research Coordinator and Principal Investigator (PI), ensures the integrity and quality of clinical trials a...
Full Time
Kingman, AZ
Posted 3 years ago
Unique opportunity to make an Impact in the healthcare industry…
IMPROVE THE FUTURE AS OUR MEDICAL ADMINISTRATIVE ASSISTANT!
Revival Research Institute, LLC is a Clinical Research organization with multiple sites located nationally throughout the United States. Established in 2015 and headquartered in the Metro-Detroit Region, Revival Research Institute now has a presence in Texas, Illinois, Arizona, and North Carolina, with experience in multiple different indications. Nationally acknowledged for our diligence to provide the highest quality of data for our clinical studies.
Importantly the Medical Assistant we select for Revival Research Institute will have an overall responsibility to enhance our operational efficiency, clinical presence, partnerships, and staff development/performance.
The qualified candidate we are looking for should be genuinely respectful of diverse points-of-view and strive for an environment in which inclusiveness drives productivity and results.
Requirements include:
- Phlebotomy Experience REQUIRED
- Lab Processing, handling & shipping
- Utilizing Good Clinical Practice, the medical assistant provides nursing care to research study patients by:
- Ensuring compliance with research protocols by reviewing all protocol requirements to confirm implementation of appropriate methods, practices, and procedures for all clinical
- Participating in recruitment and selection of study participants by interviewing and documenting medical history to determine compliance with eligibility
- Performing Clinical assessments including, but not limited to, vital sign EKGs & Venipuncture.
- Administering study medications and performing patient assessment during study visits to determine presence of side effects to medication; notifies principal investigator of findings/issues.
- Providing patient education and medical information to study patients to ensure understanding of proper medication dosage, administration, and disease
- Documenting medical data in subject chart to ensure availability of timely records for decision
- As a clinical team member, identify and prioritize the development of systems and infrastructure to maintain research quality with no supervisory
- Other duties as needed
- Willing to abide by Good Clinical Practice Guidelines and all FDA requirements
- CPR-certification preferred
- Valid MA license from the State of Arizona (Preferred)
- Minimum of a high school diploma required, advanced education preferred
- Two (2) years of recent clinical experience in a hospital, clinic, or similar health care setting. (Preferred)
- One (1) year clinical research experience (Preferred)
- Phlebotomy experience (REQUIRED)
- Must be proficient in Microsoft Office Word and Excel, electronic health systems and databases used in research environment, or willingness to learn and demonstrate proficiency within three months of hire
- Effective written, verbal, and interpersonal communication
- Excellent attention to detail
- Ability to manage multiple tasks w/ time deadlines.
- Ability to be flexible, organized, detail oriented and tenacious in follow-through.
- Possess the ability to work well under pressure
- Prioritization and organizational
- Proficient in medical terminology
- Basic drug calculation
- Problem-solving mindset
- Clinical competency skills per scope of practice (i.e., performing vital signs, clinical assessments, performing ECG/EKG, giving injections, etc.)
- Knowledge of GCP, federal, state, and local regulations, including HIPAA policies
Job Features
| Job Category | Clinical Research |
Unique opportunity to make an Impact in the healthcare industry… IMPROVE THE FUTURE AS OUR MEDICAL ADMINISTRATIVE ASSISTANT! Revival Research Institute, LLC is a Clinical Research organization with...
Are you looking for an unpaid or paid internship? Revive Research Institute is looking for college students for a three month internship opportunity located in Southfield, MI. Interns will have an opportunity to learn oncology research, dermatology research and more!
What’s the difference between unpaid and paid?
An unpaid internship is to give a general overview of clinical research such as learning regulatory, clinical, and management. A paid internship will be a focused internship where the intern will only work in either the clinical or regulatory department but will not have experience in another department.
To be eligible
- Must be an undergraduate college student
- Be able to work 15-16 hours a week
- A car to travel to different clinical sites
Job Features
| Job Category | Intern |
Are you looking for an unpaid or paid internship? Revive Research Institute is looking for college students for a three month internship opportunity located in Southfield, MI. Interns will have...