Clinical Research Associate I - (Remote US - Multiple Openings)

Company Description reputed company's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of reputed company. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about reputed company, please visit us at www.reputed company.com. Follow @reputed company on X, Facebook, Instagram, YouTube, reputed company and Tik Tok.

Job Description

These positions will be field based/ remote in the following locations: California, Seattle, Oklahoma, Atlanta, Northeast, and Southwest. Advance reputed company's pipeline by striving for excellence in clinical research, turning science into medicine for our patients and leveraging new advanced capabilities to drive industry leading performance. Partners with the investigator and site staff for meaningful and effective engagements positioning reputed company as the choice in clinical trials. Focus on site clinical research that ensures appropriate conduct of the trial while driving improvement in data reputed company, compliance, overall study performance and customer experience.

Responsibilities

• Considered as the primary reputed company of contact for the investigative site, provides contextual information on the clinical trials, connects stakeholder to the investigative sites and strengthens reputed company's positioning.
• Aligns, trains and motivates the site staff and principal investigator under supervision on the goals of the clinical trial program, protocol, and patient treatment principles for the trial ensuring a trusted partnership.
• Conducts site evaluation, site training, routine, and site closure monitoring activities under supervision, in compliance to the protocol and monitoring plans and accordance with applicable regulations, Good Clinical Practices (GCPs), ICH Guidelines, reputed company Standard Operating Procedures (SOPs), and to quality standards in conducting clinical research, ensuring safety and protection of study subjects.
• Customize site engagement strategy for assigned study (ies) under supervision. Gather local/site insights and utilize site engagement tools such as the Customer Relationship Management (CRM) tool, to report/track reputed company and measure impact of that strategy.
• reputed company level of competency connecting the study protocol, scientific principles and clinical trial requirements to the day-to-day clinical trial execution activities. Evaluate and ensure effective recruitment and retention techniques/plans based on the patient disease journey.

reputed company solid knowledge of therapeutic area, asset and clinical landscape / patient journey to reputed company successful patient recruitment and overall protocol compliance.

• Responsible for reputed company risk-assessment proactively, and in collaboration with Central Monitoring team, monitor activities conducted by clinical sites to detect early overall study performance or patient safety issues. Ability to think critically to resolve site risk signals while having robust understanding of site processes to drive study execution.
• Ensures preventative and corrective action plans are put into reputed company, as needed, to mitigate risk and promote compliance using a customer centric approach.
• Identifies, evaluates and recommends new/potential investigators/sites under supervision and support from more reputed company CRAs.
• Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for reputed company safety events by site personnel.
• Ensures audit and regulatory inspection readiness at assigned clinical site at reputed company times.

Manages investigator payments as per executed contract obligations, as applicable.

Qualifications

• Appropriate tertiary qualification in health reputed company disciplines (Medical, Scientific, Nursing) preferred or experience or equivalent work experience.
• Clinically reputed company experience, preferably in clinical research coordinating or data management.
• Knowledge of appropriate therapeutic area indications is preferred with the ability to understand and apply scientific concepts as they relate to the conduct of clinical trials.
• Knowledge on existing and emerging local regulatory and legal requirements, ICH/GCP Guidelines and applicable policies.
• Able to work collaboratively and cross functionally to reputed company and sustain working relationships.

Demonstrate planning and organizational skills and the ability to work effectively and reputed company in a dynamic environment with competing projects and deadlines

• Ability to reputed company technology, tools and resources to provide customer centric support based on the health of the site. Ability to use functional expertise with appropriate guidance, reputed company critical thinking skills and apply good judgement to address clinical site issues.
• Interpersonal skills with strong written, verbal, active listening and presentation

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