# Clinical Research Coordinator (CRC) at A.P.R., Inc.…

> Source: https://confidential.careers/job-detail/clinical-research-coordinator-crc-a-p-r-inc-alphaprotemps-kalamazoo

# Clinical Research Coordinator (CRC)

A.P.R., Inc. (AlphaProTemps) 

** Kalamazoo, United States ** Full Time ** Healthcare Jobs ** United States ** New

[Apply Now](https://confidential.careers/go/14171689) ** Save 

## Job Description

### Job Description

Job Description 3 - 6 Month Contract

Potential (Temp-to-Hire)

Fully Onsite

Monday - Friday

8:00 am - 5:00 pm

M-F 8am-5pm
FULLY On-site
Temp to hire

**Qualifications & Requirements:**

- Must have previous experience with COG
- Bachelor's degree in a scientific or healthcare field, or equivalent experience in Data entry, Research, Healthcare administration education in the protection of human research participants and Good Clinical Practices required.

**Current clinical licensure and board certifications:**

- SOCRA (preferred)
- ACRP (preferred within 4 years of hire)
- CITI training
- Human protections training
- IATA certification for shipping infectious substances and diagnostic specimens.

**Ability to read and interpret:**

- Research documents
- Clinical trial documents
- Operating and maintenance instructions
- Procedure manuals
- Strong written and verbal communication skills.
- Excellent interpersonal and relationship-building skills.

**Ability to work effectively with:**

- Physicians
- Physician offices
- Sponsors
- Hospital employees
- Strong analytical and problem-solving abilities.

**Ability to work efficiently under:**

- Tight deadlines
- High workloads
- Frequent interruptions
- Strong attention to detail and adherence to clinical trial requirements.

**Clinical Research Coordinator – Key Responsibilities**

- Prepare, submit, and monitor documentation for research programs.
- Ensure compliance with research regulations and protocols through audits.
- Advise caregivers on program design, treatment administration, and patient follow-up.
- Organize study files, including regulatory binders and source documentation.
- Maintain and update study files and records according to sponsor and institutional requirements.
- Review, edit, and update informed consent documents for clinical trials.
- Collaborate with the Principal Investigator (PI) to prepare IRB and regulatory submissions.
- Assist in reviewing eligibility criteria for participant enrollment.
- Coordinate enrollment of participants into Children's Oncology Group (COG) studies.
- Develop familiarity with COG protocols and specimen submission guidelines.
- Collect study data and ensure timely completion of Case Report Forms.
- Coordinate audits with the central COG office and maintain audit readiness.
- Perform additional duties as assigned.

**Physical & Work Environment Requirements**

- Work is mentally and visually demanding for more than 90% of the work time.
- Requires considerable standing and walking.
- Requires lifting light objects (up to approximately 20 pounds).
- May involve assisting with lifting or moving patients.
- Requires maintaining potentially fatiguing positions and performing repetitive physical movements.

**Clinical Research Coordinator (CRC):**

- For all new Trials, confirm if DTL must be created and if slide deck training is required
- Take primary responsibility for early specimen/x-ray/lab submission for RAPID EARLY Review
- Obtain parental consent for APEC14B1 (parental DNA and part B if needed)
- Maintain BMH compliance Spreadsheets with updates (quarterly, on SharePoint)
- Track patients on study and in follow-up
- Maintain Outlook Calendar for upcoming time points/appointments
- Complete all CRFs for Baseline, Reporting Period and Follow-up folders for all patients.
- Monitor SADD list weekly
- Attend daily check-in and chemotherapy rounds
- Collect all patient documents for diagnosis and treatment courses
- Prepare AE flow sheets for each therapeutic trial
- Attend CRCWM Pediatric Protocol reviews first Thursday every month at 0700
- Know investigational agents and how to get them (drug ordering)
- Prepare charts for AUDIT, attend COG meetings

**Clinical Research Coordinator (CRC) and Clinical Research Assistant (CRA):**

- CITI training/Human Protections training
- Dangerous Goods training
- Patient Registration
- Confirming eligibility/ Fast Facts reviewed
- Review all consents for correct signatures/initials on day signed
- Attend weekly COG working group meetings
- Attend Teams meetings with Helen DeVos Children’s Hospital every 2 weeks

**Maintain active account access and training for:**

- iMedidata/Rave
- COG/eRDS
- CTSU/OPEN
- Redcap*
- TRIAD*
- CRCWM

\nCompany Description AlphaProTemps is specialized in providing "best-in-class" professional staff augmentation services. These recruiting directives include temporary labor, contract sourcing, professional & technical niches, vendor-on-site, and managed service programs.

### Company Description

AlphaProTemps is specialized in providing "best-in-class" professional staff augmentation services. These recruiting directives include temporary labor, contract sourcing, professional & technical niches, vendor-on-site, and managed service programs.

Posted August 17, 2026