Research Coordinator

Memorial Healthcare is hiring a Clinical Research Coordinator to support the Principal Investigator in conducting multiple clinical research studies in compliance with research protocols and applicable regulations. The role coordinates participant screening and care, study procedures and data, regulatory compliance, staff training, and collaboration with research teams and sponsors.

Responsibilities

Ensures human subject protections via diligence in research participant screening, recruitment, consenting, enrollment, randomization, monitoring of treatment, and follow-up procedures, ongoing risk assessment related to research interventions and protocol activities

Ensures ongoing research informed consent, addresses participant questions throughout study participation, and supports their goal for participating or terminating study participation

Coordinates research activities to minimize participant risk and ensure participant safety

Distributes study article (drugs, devices), and maintains study article accountability documentation

Provides patient education and medical information to study patients to ensure understanding of proper medication dosage, administration and disease treatment

Prepares, processes and ships biological samples per study protocols and International Air Transport Association (IATA) requirements

Ensures appropriate credentialing and training of the Memorial Healthcare staff as it relates to research and protocol requirements

Ensures scientific integrity of data and maintains participant privacy, confidentiality, and safety of patients enrolled in clinical trials

Develops source documentation forms and tools per study protocol requirements

Documents all study-related procedures/events via electronic data capture systems, case report forms, etc

Communicates effectively with research participants and their families, the research team, principal investigators, external study sponsors, primary care providers (e.g., clinical nurses, physicians, etc.), ancillary staff and the IRB to ensure protocol adherence, participant safety and regulatory compliance

Participates in study site activation activities, including regulatory documentation, training of research team and impacted departments

Participates in clinical study planning for Investigator Initiated Trials, Sponsored Research Agreements

Prepares and conducts training activities for assigned trials

Assists with internal and external site audits

Supports regulatory efforts in the maintenance of regulatory documents in accordance with Memorial Healthcare Standards of Practice and applicable regulations

Assists in the maintenance of clinicaltrials.gov information for Investigator Initiated Trials and Sponsored Research Agreements

Promotes research revenue cycle best practices through the communication of protocol coverage as outline in study#s Medicare Coverage Analysis (modifier codes, and secondary diagnosis etc.)

Maintains accurate documentation of study stipend and reimburse per study protocol informed consent and budget

Acts as a liaison between site, investigators, principal investigator, Memorial Healthcare, IRBs and study sponsors

Creates study related reports as requested

Participates in meetings and provides information regarding applicable clinical trials

Participates in continuing education activities related to research to improve knowledge for job performance

Ensures compliance with research protocols by providing ongoing quality control audits

Participates with the PI and study team to identify and prioritize the development of systems and infrastructure to maintain research quality and compliance

Maintains IATA, Good Clinical Practice and other certifications as required

Occasional travel to satellite sites and to attend sponsor study training meetings as required

Performs other duties as assigned

Preferred

Bachelor#s degree in a scientific, health related, or business administration program preferred

1-2 year experience with research related activities with clinical practice, ICH guidelines, FDA and OHRP regulations, IND, SAE reporting, and protection of human research participant standards, regulations and laws preferred

Clinical Research Certification CCRC/CCRP preferred, but not required

1-2 year experience with research related activities with clinical practice, ICH guidelines, FDA and OHRP regulations, IND, SAE reporting, and protection of human research participant standards, regulations and laws preferred.

Scientific Education

Health-Related Education

Business Administration Education

Clinical Research

Clinical Practice

ICH Guidelines

FDA Regulations

OHRP Regulations

Investigational New Drug (IND) Processes

Serious Adverse Event (SAE) Reporting

Human Research Participant Protection

Clinical Research Certification (CCRC/CCRP)

Company

Community hospital and healthcare system providing patient-centered care

Owosso, Michigan, USA

http://memorialhealthcare.org/

Founded in 1921

1001-5000 employees

Qualifications

At a minimum, a candidate must have a Bachelor#s degree with recent experience in a clinical setting

Minimum 2 year prior clinical experience or equivalent clinical trial experience

MS Word, Excel, Outlook, EMR experience required

BLS

Able to navigate computer systems and enter data into database

Use of Microsoft Office Products Computer and basic office equipment proficiency required

Motivated #self-starter# with ability to exercise initiative

Detailed oriented with strong written and verbal communication skills

Able to problem solve

Identifies and resolves problems in a timely manner

Gathers and analyzes information skillfully

Analytical, prioritization and planning of work activities

Adapts for changing conditions

Ability to manage multiple priorities

Can apply effective interpersonal skills to provide service

Comfortable working in a team environment as well as independently

Adapts to changes in the work environment

Bachelor#s degree in a scientific, health related, or business administration program preferred

1-2 year experience with research related activities with clinical practice, ICH guidelines, FDA and OHRP regulations, IND, SAE reporting, and protection of human research participant standards, regulations and laws preferred

Clinical Research Certification CCRC/CCRP preferred, but not required

Minimum 2 year prior clinical experience or equivalent clinical trial experience.

Required skills

Clinical Research, ICH Guidelines, FDA Regulations, OHRP Regulations, IND Management, Serious Adverse Event (SAE) Reporting, Human Research Participant Protection, Microsoft Word, Microsoft Excel, Microsoft Outlook, Electronic Medical Records (EMR), Basic Life Support (BLS), CCRC/CCRP Certification

Preferred skills

Owosso, Michigan, USA, http://memorialhealthcare.org/, Late Stage, Leadership Team, Brian L. Long, President/CEO, Recent News, EIN Presswire, 2026-04-30, mlive, 2026-01-19, 2026-01-16, Company data provided by, AI Tools, Customize Your Resume, Maximize your interview chances, Build Cover Letter, Make your application stand out, Analyze How Well You Fit, Understand your strength & weakness

Experience

2+ years