Syneos Health LLC

Syneos Health LLC

CRC II (Onsite) - Memphis, TN

USA-TN-Client · Mid

Sponsorship not specified$68k-$115kDetected 163 days ago
GCPExcelLogisticsProcess ImprovementPhotographyClinical TrialsClinical ResearchPharmacy PracticeMedical DevicesResearchCommunicationCollaborationProblem SolvingTime Management

Stay score

odds of building a lasting career here

47Sponsors, lottery-bound
Cap-exempt (no lottery)0
Sponsors this role80
Entry-level history0
PERM / green-card track0
Lottery odds (Level II)66
Fits your clock70

Sponsors, but it's cap-subject — you still face the weighted lottery (~30% per draw at Level II). Good if you win; have a cap-exempt backup on your list.

Lottery odds assume a STEM candidate.

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About the role

  • CRC II (Onsite) - Memphis, TN 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.
  • 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.
  • Syneos complies with all applicable federal, state, and municipal paid sick time requirements.

Compensation

  • $67,700.00 - $115,100.00
  • 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)

This listing is sourced directly from Syneos Health LLC's careers page and normalized into a canonical job model.