Syneos Health LLC
Per Diem Clin Research Coordinator II - Onsite in West Monroe, Louisiana
USA-LA-Remote · Mid
Sponsorship not specified$49k-$59kDetected 51 days ago
GCPExcelLogisticsProcess ImprovementPhotographyClinical TrialsClinical ResearchPharmacy PracticeMedical DevicesResearchCommunicationCollaborationProblem SolvingTime Management
About the role
- Per Diem Clin Research Coordinator II - Onsite in West Monroe, 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.
Requirements
- Registered Nurse and/ or University Degree such as Bachelor of Science Degree required.
- Required skills: problem solving, planning, and evaluation.
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.
- Good knowledge of regulations, ICH GCP, privacy, and applicable guidelines.
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.
- Additional Information:
- Tasks, duties, and responsibilities as listed in this job description are not exhaustive.
- 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.
- Further, nothing contained herein should be construed to create an employment contract.
Benefits
- Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description.
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.
- 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.
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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This listing is sourced directly from Syneos Health LLC's careers page and normalized into a canonical job model.