Clinical Research Assistant
REVA Medical
Summary of Essential Duties and Responsibilities
The primary function in this position will be to provide departmental administrative support in the area of Clinical Affairs, including:
- Perform quality checks, uploads and tracking of required regulatory documents to populate the electronic Trial Master File (TMF) for designated studies. Generate reports of missing documents and upcoming expiration dates. Communicate with sites and/or study team to obtain required documents. Ensure the TMF is audit-ready in support of regulatory filings.
- Obtain safety-related source documents and images from clinical sites in preparation for Clinical Event Committee and Data Safety Monitoring Board meeting packages. Work with translation vendors as needed.
- Track device inventory and prepare shipments to sites, ensuring device integrity is maintained (i.e., temperature control and expiration dates). Process returned/expired devices.
- Assist with the distribution and tracking of clinical study supplies to Contract Research Organizations (CROs) and clinical centers (e.g. study binders, case report form worksheets, study devices and misc. materials)
- Interface with CROs to obtain study-related documentation and follow up on action items
- Assist with site invoicing and payment tracking
- Assist with organization and filing of study related materials
- Assist in the organization and execution of Investigator meetings
- Provide general administrative support as needed
Education and/or Experience
- Undergraduate degree
- 2-3 years of relevant clinical trial experience
Required Knowledge/Skills
- Minimum of 1-2 years of clinical study electronic Trial Master File experience
- Proficient with basic computer programs such as Microsoft Word, Excel PowerPoint and Adobe Acrobat
- Detail oriented in document review and error checking
- Effective communication skills
Desired Knowledge/Skills
- Minimum of 1-2 years of Sponsor or CRO experience
- Working knowledge of CDISC TMF Reference Model
Physical Demands/Working Environment
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this job, the employee is frequently required to sit or stand for prolonged periods of time, frequently in front of a computer.
#J-18808-Ljbffr$66.5k - $68.65k
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...Hybrid Introduction: Xencor is a public, clinical-stage biopharmaceutical company located... ...excellent opportunity for an Sr. Clinical Research Associate to join our team. This is a... ...language interpreter or other personal assistance) with the application process upon your...SuggestedFull timeWork at officeRemote work2 days per week$74.5k - $197.5k
...Clinical Research AssociateTo be eligible for this position, you must reside in the same country where the job is located.Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol...Full timePart timeLocal areaImmediate startWorldwide$38 - $65 per hour
...Clinical Research AssociateKey Responsibilities:Independently conduct pre-study, initiation, routine monitoring and closeout visits and ensures... ...non-compliance to the CTM and/or head of clinical operations.Assists the Clinical Team Lead and/or department leads of Clinical...Contract workTemporary workLocal areaImmediate startRemote work- ...Clinical Research Associate (CRA), Medical DeviceBased fully onsite in San Diego CA with some domestic clinical site travel I'm partnering with a fast-moving, commercial stage medical device company running investigational device studies. The research here moves toward...Interim role
$26 - $30 per hour
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...Job Title: Clinical Research Associate Key Responsibilities: Independently conduct pre-study, initiation, routine monitoring and... ...compliance to the CTM and/or head of clinical operations. Assists the Clinical Team Lead and/or department leads of Clinical Operations...Contract workTemporary workLocal areaImmediate startRemote work$110k - $135k
About Artiva:Artiva is clinical-stage, publicly-traded biotechnology company focused on developing... ..., visit .Job Summary:The Sr. Clinical Research Associate (CRA) supports moderately... ...(GCP) and relevant SOP's. The CRA may assist with vendor oversight and management. They...Contract workLocal areaWorldwideFlexible hours$24 - $29 per hour
Orso Health is a leading organization in clinical research, dedicated to advancing healthcare through innovative studies. We are committed to... ...and Director of Research Operations, the CRA will assist with subject scheduling, data entry, biospecimen coordination...Hourly payFor contractors- ...study training to sites Managing investigational product and clinical supplies at assigned sites Ensuring appropriate collection,... ...sciences or a nursing degree ~5+ years of relevant clinical research/healthcare experience ~ At least 2 years of direct field-monitoring...Remote work
$65 - $90 per hour
C-Clinical is looking for an experienced Senior Clinical Research Associate to support clinical trials across the San Diego region. This opportunity is ideal for professionals who enjoy working closely with investigative sites while maintaining strong oversight of complex...Hourly payRemote work$100k - $130k
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$1,768 - $1,976 per week
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$18.4 per hour
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$26 per hour
$26/hrAssay Development & BioinformaticsPosition SummaryThe Research Associate I supports cross-functional molecular diagnostics research... ...in laboratory notebooks and electronic data management systems.Assist with data compilation, quality checks, and preparation of...Work at office$27.85 - $33.22 per hour
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