Syneos Health LLC
Per Diem Clin Research Coordinator II - Onsite Lafayette, Louisiana
USA-LA-Client · Mid
Sponsorship not specified$49k-$59kDetected 167 days ago
GCPExcelLogisticsProcess ImprovementPhotographyClinical TrialsClinical ResearchPharmacy PracticeMedical DevicesResearchCommunicationCollaborationProblem SolvingTime Management
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odds of building a lasting career here
37Risky
Cap-exempt (no lottery)0
Sponsors this role80
Entry-level history0
PERM / green-card track0
Lottery odds (Level I)39
Fits your clock70
Thin sponsorship signal and lottery-bound (~15% per draw). A low-probability bet with your clock running. Prioritize cap-exempt roles and proven entry-level sponsors first.
Lottery odds assume a STEM candidate.
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About the role
- Per Diem Clin Research Coordinator II - Onsite Lafayette, Louisiana Illingworth Research Group provides a range of patient focused clinical services to the pharmaceutical, healthcare, biotechnology and medical device industries.
- These include mobile research nursing, patient concierge, medical photography and clinical research services.
- Illingworth are experts with experience across all study phases and in a diverse range of therapeutic areas.
Responsibilities
- Further, nothing contained herein should be construed to create an employment contract.
- The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
- Prepare and maintain the Investigator Site File and/ or Trial Master File (TMF) for the study.
- Support the Principal
Requirements
- Registered Nurse and/ or University Degree such as Bachelor of Science Degree required.
- Good knowledge of regulations, ICH GCP, privacy, and applicable guidelines.
- Required skills: problem solving, planning, and evaluation.
- Occasionally, required skills/experiences for jobs are expressed in brief terms.
- Take the lead and/or overall coordination of all required start-up activities including, but not limited, to the following:
- Confirms all required regulatory and contractual documentation is present prior to study start.
Nice to have
- Clinical Research certification preferred.
- A minimum of 1 year experience in clinical research required, preferably in coordination of clinical research projects.
- 2+ years preferred.
Skills
- Possess good time management, detail-oriented, and able to multi-task.
- Knowledge of SOP writing.
- Ability to anticipate problems and provide solutions in a timely manner.
- Ability to coordinate multiple clinical research projects with competing deadlines.
- Proficiency in computer software programs (e.g. Word, Excel, Power Point).
- Proficiency in use of various clinical trial EDC software preferred.
- problem solving, planning, and evaluation.
- The hourly rate will be disclosed during the recruitment process and will comply with all relevant federal, state, and local wage laws"
Compensation
- The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on various factors such as the candidate's qualifications, skills, competencies, and proficiency for the role.
Company info
- The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities.
- The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above.
Visa & Work Authorization
- Participate in creation and review of timelines and start-up meetings (Investigator Meeting/SIV, Sponsor discussions, or other related meetings)
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