Clinical Research Associate Jobs

One of our clients is seeking a talented and highly motivatedClinical ResearchAssociate. Pleasesend your resumeif you would like to pursue this opportunity and authorize Infosoft to represent you for this position.

Here are the job position details for your review:

Job Title:Clinical ResearchAssociate

Pay Rate: $45 to49.50/Hr

Duration:12 Months

Location:Orange County, CA (onsite)

Our Client is aGlobal Medical Device Manufacturer.

We are looking for aClinical ResearchAssociate.As the Clinical ResearchAssociate, you will be responsible for providing project management of dynamic and high-volume core lab projects across allglobal clinical studiesto ensure the accurate and timely transfer of images fromstudy sitesto Independent Core Labs, andclinical datafrom Independent Core Labs to clients' data management teams to ultimately provide unbiased study results.

Coming from a Clinical Analyst background, lots oftrialswill be conducted, working will different cross-functional team, working with Core Labs and vendors for image gathering, a good job for someone who enjoys working with people, and will work on something different every week, will require a lot of thinking, and it is a great team and they are growing in the department!

• Analyze the clinical output of moderately complex studies and provide a high-level summary with supporting details ofstudy trial status(e.g., Core Lab image perspective) to stakeholders and clinical management
• Provide guidance and represent the department to communicate risk and impact to study the core team's key milestones and deliverables
• Assist in the development of training material content in collaboration with clinical stakeholders for clinical sites and clinical field staff
• Develop basic timeline assessment and/or work with senior-level team members on complex timeline assessment (e.g., clinical site through Image workflow vendor to Independent Core Lab) in collaboration with clinical stakeholders in order to meet key study milestones and deadlines
• Identify, develop, recommend, and implement moderately complex process development and process improvement solutions to optimize global trial workflow timelines, (e.g., open information requests, aging issues, the status of the image analysis from Core Labs to study database, etc.)
• Identify technical and data issues and collaborate with appropriate team members to bring them to resolution; assist in the determination of root cause and recommend and implement corrective actions

Minimum Requirements:

• Bachelor's Degree in a related field
• 3 years of previous hands-onclinical researchexperience

Additional Skills:

• Good problem-solving, organizational, analytical, and critical thinking skills
• Must be able to work in a team environment, including inter-departmental teams and representing the organization on specific projects
• Good computer skills in usage of MS Office Suite including MS Project and excellent Excel skills required
• Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of the environment and prevention of pollution under their span of influence/control
• Ability to manage competing priorities in a fast-paced environment
• Excellent written and verbal communication skills and interpersonal relationship skills
• Solid knowledge of human anatomy and physiology
• Ability to interact professionally with all organizational levels
• Strict attention to detail
• Solid understanding and knowledge of principles, theories, and concepts relevant to clinical trial management