Clinical Research Associate II - Oncology & Neurology (WA, OR, ID, MT, WY, CO)

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Clinical Research Associate (Level II) - Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. As part of our global team, you will perform and coordinate all aspects of the clinical monitoring and site management process. As a Clinical Research Associate (Level II), you will conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation. You will manage procedures and guidelines from different sponsors and/or monitoring environments (i.e., FSO, FSP, Government, etc.). Acting as a site processes specialist, you will ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, well-being, and data reliability. You will ensure audit readiness and develop collaborative relationships with investigational sites. The task matrix outlines detailed responsibilities for your role. This is an opportunity for experienced CRAs with explicit on-site monitoring experience. Oncology and/or Neurology therapeutic experience is highly preferred. Candidates must be located in WA, OR, ID, MT, WY, CO within 60 miles of the nearest major airport. Up to 80 percent travel is expected. Must be legally authorized to work in the United States without sponsorship. Must be able to pass a comprehensive background check, which includes a drug screening. Essential Functions Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis, critical thinking and problem-solving skills to identify site process failures and corrective/preventive actions to bring the site into compliance and decrease risks. Ensures data accuracy through SDR, SDV and CRF review as applicable through on-site and remote monitoring activities. Assesses investigational product through physical inventory and records review. Documents observations in reports and letters in a timely manner using approved business writing standards. Escalates observed deficiencies and issues to clinical management expeditiously and follows all issues through to resolution; maintains regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, previously identified issues are being resolved and the data is being recorded in a timely manner. Conducts monitoring tasks in accordance with the approved monitoring plan. Participates in the investigator payment process. Ensures a shared responsibility with other project team members on issues/findings resolution; investigates and follows up on findings as applicable. Participates in investigator meetings as necessary; identifies potential investigators in collaboration with the client company to ensure the acceptability of qualified investigative sites. Initiates clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted. Performs trial close out and retrieval of trial materials. Ensures that required essential documents are complete and in place, according to ICH-GCP and applicable regulations. Conducts on-site file reviews as per project specifications. Provides trial status tracking and progress update reports to the Clinical Team Manager as required. Ensures study systems are updated per agreed study conventions (e.g. Clinical Trial Management System). Facilitates effective communication between investigative sites, the client company and the PPD project team through written, oral and/or electronic contacts. Responds to company, client and applicable regulatory requirements/audits/inspections. Maintains and completes administrative tasks such as expense reports and timesheets in a timely manner. Contributes to the project team by assisting in preparation of project publications/tools and sharing ideas/suggestions with team members. Contributes to other project work and initiatives for process improvement, as required. Education and Experience Requirements Bachelor's degree in a life sciences related field or a Registered Nursing certification or equivalent and relevant formal academic or vocational qualification. Previous experience that provides the knowledge, skills, and abilities to perform the job comparable to 1 year as an on-site clinical research monitor or completion of PPD Drug Development Fellowship. Oncology and/or Neurology therapeutic experience is highly preferred. Valid driver's license where applicable. Candidates must be located in WA, OR, ID, MT, WY, CO within 60 miles of the nearest major airport. Up to 80 percent travel is expected. In some cases, an equivalency consisting of a combination of appropriate education, training and/or directly related experience may be considered sufficient to meet the requirements of the role. Knowledge, Skills and Abilities Proven clinical monitoring skills. Demonstrated understanding of medical and therapeutic area knowledge and medical terminology. Demonstrated ability to attain and maintain a working knowledge of ICH GCPs, applicable regulations and procedural documents. Well-developed critical thinking skills, including a critical mindset, in-depth investigation for appropriate root cause analysis and problem solving. Ability to manage Risk Based Monitoring concepts and processes. Good oral and written communication skills, with the ability to communicate effectively with medical personnel. Ability to maintain customer focus through utilization of good listening skills, attention to detail and the ability to perceive customers' underlying issues. Good organizational and time management skills. Effective interpersonal skills. Attention to detail. Ability to remain flexible and adaptable in a wide range of scenarios. Ability to work in a team or independently as required. Good computer skills: solid knowledge of Microsoft Office and ability to learn appropriate software. Good English language and grammar skills. Good presentation skills. Working Conditions and Environment Work is performed in an office, laboratory, clinical and/or home office environment with exposure to electrical office equipment. Frequent travel to site locations; generally 60 to 80 percent but more for some individuals; may also include extended overnight stays. Exposure to biological fluids with potential exposure to infectious organisms. Personal protective equipment required such as protective eyewear, garments and gloves. Exposure to fluctuating and/or extreme temperatures on rare occasions. Salary Transparency This is a salaried role that will also be eligible to receive a variable annual bonus based on company, team and/or individual performance results in accordance with company policy. Compensation will be initially discussed during the screening period, with actual compensation confirmed in writing at the time of offer. We offer a comprehensive Total Rewards package that our United States colleagues and their families can count on, which generally includes: Choice of national medical and dental plans and a national vision plan. Wellness program and valuable health incentive opportunities for company contributions to Health Reimbursement Accounts or Health Savings Account. Tax-advantaged savings and spending accounts and commuter benefits. Employee assistance programs. At least 120 hours paid time off, 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, short and long-term disability. Retirement and savings programs such as a competitive 401(k) retirement savings plan. Compensation and Benefits The salary range estimated for this position based in Oregon is $66,800 to $125,000. More Information on Benefits For more information on our benefits, please visit #J-18808-Ljbffr Remote Jobs