Syneos Health

CRC II (Onsite) - Marietta, GA

USA-GA-Client · Mid

Sponsorship not specified$68k-$115kDetected 28 days ago

GCPExcelLogisticsProcess ImprovementPhotographyClinical TrialsClinical ResearchPharmacy PracticeMedical DevicesResearchCommunicationCollaborationProblem SolvingTime Management

About the role

CRC II (Onsite) - Marietta, GA 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.
Perform all study activities following Good Clinical Practices (GCP).
Manage multiple clinical trials simultaneously.
Develop patient rapport to explain research protocols and minimize protocol violations.
Develop rapport with study team to educate team on study procedures and minimize protocol violations.
Take the lead and/or overall coordination of clinic activities including, but not limited to:
Review and manage clinic updates, Adverse Event (AE) or Serious Adverse Events (SAEs) reporting, study logs and tracker, quality control, and Monitor findings.

Requirements

Registered Nurse and/ or University Degree such as Bachelor of Science Degree required.
Good knowledge of regulations, ICH GCP, privacy, and applicable guidelines.
Take the lead and/or overall coordination of all required start-up activities including, but not limited, to the following:
Preparation, review, and/or finalization of clinic source documents, time and events tables, and other required study materials
Confirms all required regulatory and contractual documentation is present prior to study start.
Occasionally, required skills/experiences for jobs are expressed in brief terms.
Coordinate and monitor screening activities; provides support as required.
Submit data in required timeframe.
Respond to inquiries by auditors for data clarification or additional data in required timeframe.
Supervises clinic visits (admission, dosing and randomization, discharge, and follow-up) as required and provides on-call support when applicable.

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.

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.

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's careers page and normalized into a canonical job model.