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

Remote, USAFull-timePosted 2026-07-28

reputed company 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 reputed company to have a remarkable reputed company 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, reputed company, Instagram, YouTube, reputed company and reputed company. Job reputed company 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 reputed company 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. reputed company 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 reputed company 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 reputed company Operating Procedures (SOPs), and to reputed company standards in conducting clinical research, ensuring safety and protection of study subjects.
  • Customize site engagement reputed company for assigned study (ies) under supervision. reputed company local/site insights and utilize site engagement tools such as the Customer Relationship Management (CRM) tool, to report/reputed company reputed company and measure reputed company of that reputed company.
  • 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 reputed company.

reputed company solid knowledge of therapeutic area, asset and clinical landscape / patient reputed company 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 reputed company plans are put into reputed company, as needed, to mitigate risk and promote compliance using a customer reputed company approach.
  • Identifies, evaluates and recommends new/potential investigators/sites under supervision and support from more reputed company CRAs.
  • Ensures reputed company of data submitted from study sites and assures reputed company 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.
  • reputed company 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 reputed company and deadlines

  • Ability to reputed company technology, tools and resources to reputed company customer reputed company 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, reputed company listening and presentation skills, with ability to establish and reputed company site relationships and trusted partnerships through engagement, motivation, and training.
  • Acts with reputed company in accordance with reputed company reputed company of business conduct and leadership values. Self-motivated individual reputed company on delivering reputed company and reputed company reputed company in a fast-paced environment.

Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:

  • The compensation reputed company described below is the reputed company of possible reputed company pay compensation that reputed company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation reputed company reputed company this reputed company will depend on many factors including geographic location, and we may ultimately pay more or less than the posted reputed company. This reputed company may be modified in the reputed company.
  • We offer a comprehensive package of benefits including reputed company time off (vacation, holidays, reputed company), medical/dental/reputed company insurance and 401(k) to eligible employees.
  • This job is eligible to participate in our short-term incentive programs.

Note: No reputed company of pay is considered to be wages or compensation until such reputed company is reputed company, reputed company, and determinable. The reputed company and availability of any bonus, commission, incentive, benefits, or any other reputed company of compensation and benefits that are allocable to a particular employee remains in reputed company's sole and absolute discretion unless and until reputed company and may be modified at reputed company's sole and absolute discretion, consistent with applicable law. reputed company is an equal opportunity employer and is committed to operating with reputed company, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit https://www.reputed company.com/join-us/equal-employment-opportunity-employer.reputed company US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.reputed company.com/join-us/reasonable-accommodations.reputed company Apply tot his job Apply To this Job

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