Clinical Research Coordinator
Wyoming, Michigan, United States · ਪੂਰਾ ਸਮਾਂ
ਅਰਜ਼ੀ ਦੇਣ ਵਾਲੇ ਪਹਿਲੇ ਵਿਅਕਤੀ ਬਣੋ
- ਅਨੁਭਵ
- Up to 5 yrs
- ਤਨਖਾਹ
- —
- ਖੁੱਲ੍ਹਣ ਵਾਲੀਆਂ ਥਾਵਾਂ
- 1
- ਪੋਸਟ ਕੀਤਾ ਗਿਆ
- 3 ਘੰਟੇ
- ਕੰਮ ਮੋਡ
- ਦਫ਼ਤਰ ਵਿੱਚ
- ਸਿੱਖਿਆ
- ਬੈਚਲਰ ਡਿਗਰੀ
- ਯੋਗਤਾ
- Candidates with a background in life sciences or related healthcare fields and 0–5 years of relevant experience can apply. Preference is given to applicants who can demonstrate clinical research exposure, regulatory knowledge, and, where applicable, certification readiness or prior experience in me…
- ਰੈਜ਼ਿਊਮੇ
- ਅਰਜ਼ੀ ਦੇਣ ਲਈ ਲੋੜੀਂਦਾ ਹੈ
ਤੁਸੀਂ ਕਿੱਥੇ ਕੰਮ ਕਰੋਗੇ
ਕੰਮ ਦਾ ਵੇਰਵਾ
About the Role
We are looking for a highly organized Clinical Research Coordinator to run the day-to-day activities of clinical trials. This role is the key connection point between the study site, sponsors, and regulatory authorities, with responsibility for maintaining strong patient safety, data quality, and compliance with standards such as ICH-GCP and FDA 21 CFR.
Core Responsibilities
- Handle the operational flow of clinical studies, including participant recruitment, screening, enrollment, and scheduled follow-up visits.
- Keep Essential Document files complete and current, and make sure all study work follows IRB/IEC expectations and internal SOPs.
- Enter study information accurately into Electronic Data Capture systems and follow ALCOA+ data integrity principles.
- Track participant safety, and report adverse events and serious adverse events quickly to sponsors and oversight bodies.
- Prepare and maintain source records, and support internal and external audits to help meet GxP and cGMP standards.
- Act as the main contact for Clinical Research Associates during monitoring visits.
Qualifications
A bachelor’s degree in Life Sciences, Nursing, Biomedical Sciences, or another related healthcare discipline is required. The role calls for 0 to 5 years of experience in clinical research, healthcare administration, or academic laboratory settings.
Applicants should have a solid grasp of ICH-GCP, human subject protection, clinical trial management tools, EDC systems, and 21 CFR Part 11 requirements for electronic records and signatures. Strong medical writing and documentation ability is also needed.
Preferred qualifications include eligibility for or certification in CCRC (ACRP) or CCRP (SoCRA), experience with medical device trials under ISO 14155, and familiarity with phlebotomy or basic clinical assessment tasks.
What We Offer
This opportunity includes focused placement support with hiring managers in the Life Sciences and MedTech sectors, help in rebuilding your resume to showcase clinical and regulatory strengths, and interview coaching covering behavioral questions and compliance-based case scenarios.
Application Note
Interested candidates should send an updated resume to [email protected].