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Clinical Research Associate

4 months ago

Fort Worth, United States Randstad USA Full time
job summary:
As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you

 
location: Fort Worth, Texas
job type: Contract
salary: $71.43 - 85.71 per hour
work hours: 9 to 5
education: Bachelors
 
responsibilities:
Site Selection and Initiation:

Assist in the selection of investigative sites for clinical trials.Conduct site initiation visits to verify that site staff are properly trained and delegated to perform protocol assessments, are familiar with regulatory requirements, and understand proper handling and storage of ophthalmic drugs / devices.Ensure recruitment strategies are in place to meet enrollment targets.Confirm that site meets requirements to begin screening subjects. Monitoring and Site Management:

Conduct on-site and remote monitoring visits according to the protocol monitoring plan to ensure data quality and regulatory compliance.Review source documents, case report forms, and patient records.Verify the informed consent process is properly executed and adherence to the study protocol.Ensure that instruments / equipment used in the clinical trials are correctly calibrated, maintained, and utilized according to the study protocol and regulatory standards.Collaborate with Clinical Operations Lead and Clinical Trial Team (CTT) to identify and resolve site quality or study execution issues. Regulatory Compliance:

Ensure that the clinical trial sites are compliant with applicable regulatory requirements (e.g., FDA, ICH, GCP, ISO) regarding ophthalmic drugs / devices.Ensure that study sponsor and Investigator Site File is maintained and audit ready.Assists sites and CTT with internal and external audit / inspection-related activities including preparation, defining CAPAs, and ensuring CAPA targets are met. Investigational Product (IP) and Clinical Supplies Oversight:

Verify subject qualification and correct IP was dispensed / implanted.Ensure masking has been maintained, if applicable.Confirm full reconciliation of IP at the site level.Monitor drug / device-related safety and performance concerns and report them to the study sponsor.Ensure proper handling, storage, and accountability of investigational drugs and/or devices.Ensures appropriate clinical supplies are available, within expiry date and adequate for clinical trial. Data Management:

Verify data accuracy and completeness, including instrument / equipment-generated data. Ensure data is securely stored.Collaborate with data management team to resolve data-related issues. Safety Reporting:

Ensure all safety issues are communicated and managed by the Principal Investigator according to regulatory and protocol requirements. Close-Out Visits:

Conduct close-out visits to ensure study documentation is complete, finalize data collection, and ensure all study-related activities are completed in accordance with the study protocol and regulatory requirements.Review Investigator obligations. Documentation and Reporting:

Complete comprehensive and accurate monitoring reports, including site follow-up letters.Ensure CTMS and eTMF are up to date and audit ready.  
qualifications:
Bachelor's degree in a related field (life sciences, nursing, etc.).Previous experience as a Clinical Research Associate, preferably in ophthalmology or a related therapeutic area.Knowledge of ophthalmic diseases, treatments, and related medical terminology, including ophthalmic devices.Strong understanding of clinical research regulations and Good Clinical Practice (GCP) guidelines.Excellent communication and interpersonal skills.Attention to detail and the ability to work independently and as part of a team.Willingness to travel as needed for on-site monitoring visits.Certification as a Certified Clinical Research Associate / Professional (CCRA / CCRP) or similar credential is a plus. 
skills: CRF, Clinical research, MS-WORD, MS-EXCEL, MS-Powerpoint, GCP (Good Clinical Practice), COV (Close-Out Visit), CTMS (Clinical Trial Management Systems), EDC (Electronic Data Capture), PSV (Pre-Study Visit), RMV (Routine Monitoring Visit), SIV (Site Initiation Visit), ICH Regulations, TMF

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.

Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).

Applications accepted on ongoing basis until filled.