$23 - $30.50/hr
Consults with the Site Manager and virtual Clinical Research Coordinator to ensure compliance with ... guidelines * Reviews the medical and social history of members * Assist in building the community ...
$23 - $30.50/hr
Consults with the Site Manager and virtual Clinical Research Coordinator to ensure compliance with ... guidelines * Reviews the medical and social history of members * Assist in building the community ...
Garden City, MI · On-site
$23 - $30.50/hr
Consults with the Site Manager and virtual Clinical Research Coordinator to ensure compliance with ... guidelines * Reviews the medical and social history of members * Assist in building the community ...
Garden City, MI · On-site
$23 - $30.50/hr
Consults with the Site Manager and virtual Clinical Research Coordinator to ensure compliance with ... guidelines * Reviews the medical and social history of members * Assist in building the community ...
We are seeking a highly experienced Science Hiring Manager with a strong track record of hiring for research laboratories, clinical trial teams, and bench-based scientific environments. This role ...
We are seeking a highly experienced Science Hiring Manager with a strong track record of hiring for research laboratories, clinical trial teams, and bench-based scientific environments. This role ...
Clinical Research (RN position - Detroit) Scheduled Bi-Weekly Hours: 80 Shift: Full-Time Days Daily ... Responsible for managing patient standard of care needs as well as participant and protocol needs ...
Clinical Research (RN position - Detroit) Scheduled Bi-Weekly Hours: 80 Shift: Full-Time Days Daily ... Responsible for managing patient standard of care needs as well as participant and protocol needs ...
Department: Clinical Research (RN position - Detroit) Scheduled Bi-Weekly Hours: 80 Shift ... Responsible for managing patient standard of care needs as well as participant and protocol needs ...
Department: Clinical Research (RN position - Detroit) Scheduled Bi-Weekly Hours: 80 Shift ... Responsible for managing patient standard of care needs as well as participant and protocol needs ...
Department: Clinical Research (RN position - Detroit) Scheduled Bi-Weekly Hours: 80 Shift ... Responsible for managing patient standard of care needs as well as participant and protocol needs ...
Department: Clinical Research (RN position - Detroit) Scheduled Bi-Weekly Hours: 80 Shift ... Responsible for managing patient standard of care needs as well as participant and protocol needs ...
Ann Arbor, MI · On-site
$23.75 - $31.50/hr
As a clinical research Intermediate for The Mary H. Weiser Food Allergy Center (MHWFAC) we expect ... Managing purchase of supplies, coordinating purchases with research and administrative staff as ...
Ann Arbor, MI · On-site
$23.75 - $31.50/hr
As a clinical research Intermediate for The Mary H. Weiser Food Allergy Center (MHWFAC) we expect ... Managing purchase of supplies, coordinating purchases with research and administrative staff as ...
Southfield, MI · On-site
$60K - $72K/yr
Clinical Research Coordinator in Southfield, MI (48075) Overview: We are seeking a detail-oriented ... Manage all aspects of study coordination including participant recruitment, informed consent, visit ...
New
Southfield, MI · On-site
$60K - $72K/yr
Clinical Research Coordinator in Southfield, MI (48075) Overview: We are seeking a detail-oriented ... Manage all aspects of study coordination including participant recruitment, informed consent, visit ...
New
$24 - $32/hr
Liaising with Laboratory team, Data team, Administrative staff, Clinical Investigators, Research Participants and Sponsor/CRO representatives, under the direction of the Site/Study Management Team ...
$24 - $32/hr
Liaising with Laboratory team, Data team, Administrative staff, Clinical Investigators, Research Participants and Sponsor/CRO representatives, under the direction of the Site/Study Management Team ...
Ann Arbor, MI · On-site
$45K - $55K/yr
Our Clinical Research Coordinators are responsible for executing and revising a set of protocols ... Managing and maintaining subject and laboratory study data * Troubleshooting and solving routine ...
New
Ann Arbor, MI · On-site
$45K - $55K/yr
Our Clinical Research Coordinators are responsible for executing and revising a set of protocols ... Managing and maintaining subject and laboratory study data * Troubleshooting and solving routine ...
New
Almont, MI · On-site
$19.50 - $26.48/hr
... with supporting clinical research and research studies at Intermountain Healthcare. A key ... Sample Management: Assist in the collection, preparation, shipment, and evaluation of laboratory ...
Almont, MI · On-site
$19.50 - $26.48/hr
... with supporting clinical research and research studies at Intermountain Healthcare. A key ... Sample Management: Assist in the collection, preparation, shipment, and evaluation of laboratory ...
Clinical Research QA Education Project Manager This role sits within the Quality team supporting the Cancer, Clinical Trials and Translational Research Office and focuses on designing, delivering ...
Quick apply
Clinical Research QA Education Project Manager This role sits within the Quality team supporting the Cancer, Clinical Trials and Translational Research Office and focuses on designing, delivering ...
Be Seen First
Kalamazoo, MI · On-site
$44/hr
Research documents * Clinical trial documents * Operating and maintenance instructions * Procedure ... managed service programs.
Quick apply
Be Seen First
Kalamazoo, MI · On-site
$44/hr
Research documents * Clinical trial documents * Operating and maintenance instructions * Procedure ... managed service programs.
Some responsibilities will include coordinating and managing multiple studies. They are also ... other clinical staff, with any study related tasks as follows but not limited to: * Research ...
Quick apply
Some responsibilities will include coordinating and managing multiple studies. They are also ... other clinical staff, with any study related tasks as follows but not limited to: * Research ...
Some responsibilities will include coordinating and managing multiple studies. They are also ... other clinical staff, with any study related tasks as follows but not limited to: * Research ...
Some responsibilities will include coordinating and managing multiple studies. They are also ... other clinical staff, with any study related tasks as follows but not limited to: * Research ...
Department: Clinical Research (RN position - Detroit) Scheduled Bi-Weekly Hours: 80 Shift ... Responsible for managing patient standard of care needs as well as participant and protocol needs ...
Department: Clinical Research (RN position - Detroit) Scheduled Bi-Weekly Hours: 80 Shift ... Responsible for managing patient standard of care needs as well as participant and protocol needs ...
Department: Clinical Research (RN position - Detroit) Scheduled Bi-Weekly Hours: 80 Shift ... Responsible for managing patient standard of care needs as well as participant and protocol needs ...
Department: Clinical Research (RN position - Detroit) Scheduled Bi-Weekly Hours: 80 Shift ... Responsible for managing patient standard of care needs as well as participant and protocol needs ...
Responsible for managing patient standard of care needs as well as participant and protocol needs ... Provides clinical research support staff with the documentation needed to determine eligibility and ...
Responsible for managing patient standard of care needs as well as participant and protocol needs ... Provides clinical research support staff with the documentation needed to determine eligibility and ...
Ann Arbor, MI · On-site
$23.75 - $31.50/hr
... Management and Informatics 7. Leadership and Professionalism 8. Communication and Teamwork The research assistant will support all aspects of the research process including: * Administer ...
Ann Arbor, MI · On-site
$23.75 - $31.50/hr
... Management and Informatics 7. Leadership and Professionalism 8. Communication and Teamwork The research assistant will support all aspects of the research process including: * Administer ...
Clinical Research RN Under the supervision of the Director of Clinical Research, the Clinical ... management, and drug/device accountability. Coordinate and perform study specific regulatory ...
Clinical Research RN Under the supervision of the Director of Clinical Research, the Clinical ... management, and drug/device accountability. Coordinate and perform study specific regulatory ...
The most popular types of Clinical Research Informatics jobs in Michigan are:
For Manager Clinical Research Informatics jobs in Michigan, the most frequently searched job titles are:
The top searched job categories for Manager Clinical Research Informatics jobs in Michigan are:
Cities in Michigan with the most Manager Clinical Research Informatics job openings:
$23 - $30.50/hr
Part-time
Medical, Dental, Vision, Retirement, PTO
Re-posted 9 days ago
5.0
Based on 10 frontline employees who took The Breakroom Quiz
Put your talents to work at PCM! Whether you work in our Home Care, Clinical Research, Impairments, or Catastrophic Care division, you will support our mission to deliver care and other services that enhance the quality of life of our clients. Be a part of our dynamic client-focused team and make a difference in your career!
As an on-site Clinical Research Coordinator (CRC), you will provide technical and administrative support to your assigned clinical operations team in the field as well as direct patient care of research study participants. You work with a high attention to detail, reviewing documentation, coordinating clinical study project details, and maintaining data systems - all with a sense of urgency aligned with that of our customers. The position will involve the conduct of trial coordinator activities for EmVenio Research' decentralized network. This will include assessing and following trial participants along with other trial protocol-related activities. In this role the CRC is accountable for the regulatory compliance and performance of assigned mobile clinics and clinician teams conducting decentralized trials as well as patient engagement, and screening. Additional focus will be on timely and accurate EDC data entry and query resolution.QUALIFICATIONS
Proven ability to communicate effectively within an interdisciplinary team to ensure safe, efficient, quality patient care, both in-person and virtually.
Excellent organizational skills and strong attention to detail, with proven ability to handle multiple tasks efficiently and effectively.
Ability to effectively analyze project specific data/systems to ensure accuracy and efficiency.
Flexibility to reprioritize workload to meet changing project timelines.
Responsible for adhering to FDA Good Clinical Practices, FDA regulations, EmVenio Research/Client Standard Operating Procedures and Working Practice Documents regulations for all non-clinical/clinical aspects of project implementation, execution, and closeout.
Ability to successfully complete EmVenio Research clinical training program.
Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.
Must have strong interpersonal skills to be able to interact with multiple people on many different levels.
May be responsible for basic clinical assessments.
ESSENTIAL FUNCTIONS/AREAS OF ACCOUNTABILITY
Complete study tasks as outlined by trial protocol
Ensures documentation is accurate according to EmVenio guidelines and protocols is required
Achieves EmVenio standards for quality, customer service, productivity and teamwork through participation in Risk and Quality Improvement programs, clinical meetings and other meetings as required
Works collaboratively with nurses, physicians, nurse practitioners, physician assistants, clinical research specialists, leaders, family members, key care givers and any ancillary medical personnel as appropriate
Communicates with key stakeholders such as the Principal Investigator, clinical trials team and quality department, regulatory
Certain assignments may require provider to perform ECGs, draw blood (Phlebotomy), process and ship lab specimen, etc.
Consults with the Site Manager and virtual Clinical Research Coordinator to ensure compliance with guidelines
Reviews the medical and social history of members
Assist in building the community research site network and developing relationships within that community
Participates in recruitment of participants to include personally engaging the general public face to face in local across hard-to-reach communities, attending community events, speaking with physicians and people across diverse cultures and backgrounds to support meeting participant enrollment targets
Documenting recruiting efforts and outreach progress
Facilitates conversations with potential participants through both inbound and outbound calls sometimes serving as their first introduction to research
Participates in all mandatory compliance, patient engagement and other training programs, seeks guidance for compliance-related concerns and adheres to all applicable laws, regulations and EmVenio policies and procedures
Maintains positive control of all PHI information
Participates in required training and education programs
Ensures adherence to clinical trial protocols and supports the clinical trials team in ensuring that trials are conducted and comply with all regulatory, state, national and internationally accepted guidelines for Good Clinical Practice (ICH GCP).
Ensures timely and accurate data collection and completion of case report forms relevant to clinical trials or research projects.
Assists in liaising with monitors of clinical trials and available to monitor and/or audit when required, with full patient documentation available.
Assists in educating EmVenio Research staff and participants regarding the designated clinical trial and procedures and relevant investigations associated with the designated clinical trial and to raise the profile of research throughout the EmVenio Research.
Any other duties needed to help drive EmVenio's purpose, fulfill our mission, and abide by our core values.
Individual base pay depends on various factors, in addition to primary work location, complexity and responsibility of role, job duties/requirements, and relevant experience, skills and other market-based factors.
Available Benefits Include
Professional Case Management is an Equal Opportunity Employer.
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Since 1997, Professional Case Management (PCM) has been providing quality, nationwide in-home nursing services to sufferers of chronic diseases. We are the nation's premier healthcare provider for nuclear weapons workers, uranium miners, millers and haulers suffering from illnesses contracted in the course of their employment. Our mission is to deliver quality care to enhance patient outcomes in the privacy and comfort of their homes.
Health care and social assistance
201 - 500 Employees
Denver, CO, US
1986
