Site Monitor

About Discovery Life Sciences:Discovery Life Sciences (Discovery) is a leading provider of highly characterized human biospecimens and cellular starting materials to advance cell and gene therapy and precision medicine programs for cancer, infectious disease, and other complex conditions. We routinely manage hundreds of studies and expertly test thousands of biospecimens simultaneously. Leading biopharma, diagnostic and academic institutions trust us to quickly deliver high-quality biospecimens and reliable, reproducible biomarker data, so they can outpace their competition and push the leading edge of innovation using our Science at your Service TM business model. Position Summary:The Site Monitor, Clinical Affairs contributes to our mission by monitoring our clinical site network which supports data quality and integrity and ensures adherence to procedures and protocols. This individual will collaborate with other members of the Clinical Affairs team to monitor while working cross-functionally with internal and external stakeholders to execute processes for maximum effective and efficient performance. A Day in the Life of a Manager, Clinical Affairs at Discovery Life Sciences:Conduct and Document Site Monitoring: Perform regular remote or on-site monitoring visits to ensure compliance with clinical protocols, resolve outstanding issues, and compile detailed monitoring reports.Partner with Clinical Teams: Collaborate with Clinical Affairs Managers and site personnel to ensure accurate regulatory documentation, data integrity, and protocol adherence across clinical trial sites.Proactively Address Site Issues: Identify and resolve site-specific challenges—supporting retraining, corrective actions, and continuous process improvements to maintain quality standards.Stay Organized and Travel-Ready: Manage timelines and documentation across multiple sites while traveling up to 50% of the time to support ongoing clinical trials and site performance. Must-Have Qualifications (Education, Skills, Experience):5+ years of experience in clinical trial research with monitoring oversight preferred3-5 years of comparable or related medical experience Experience in a clinical research organization or oncology/infectious disease/autoimmune therapeutic specialties with familiarity of principles, concepts, standards of care and clinical study designHighly developed organizational and analytical skills with the ability to multitask, prioritize time-sensitive activities and work both independently and as part of a team in a matrix environmentExcellent presentation, communication and relationship-building skillsThrive in a challenging and results-oriented work environmentDemonstrate ability to develop trust and maintain integrity with external clinical and scientific experts, institutions, peers, and othersProven ability to analyze problems, develop and implement strategic solutions to optimize and maximize systems Ability to work independently as well with interdisciplinary teams (internal and external) Strong proficiency with MS SuiteSalesForce.com and MediaLab experience is desirable but not requiredAbility to travel to clinical sites up to 50% of the timePreferred home base near an international airportExperience with electronic medical records (EMR) is desirable but not required Key Responsibilities:Manage, coordinate, and support clinical site monitoring activitiesConduct visits and partner with the Clinical Affairs Manager to schedule the visit, obtain proper access, and complete the overall Monitoring plan. This includes preparing reports and all applicable correspondencePerform general monitoring functions of review data according to monitoring guidelines, ensure all documentation is present, and compile findingsMonitor on client projects as required by researchers, biopharmaceutical, etc., including enrollment updatesResolve issues from previous visits, address protocol questions, and ensure outstanding documents are completed properlyCollect regulatory documentation, file properly, and ensure accuracyUpdate site specific filesPartner with Quality and the site’s Clinical Affairs Manager on promptly reportable incidents (PRIs)Resolve site and/or monitoring issues including appropriate retraining, issue escalation, and implementation of corrective actions to prevent recurrence, as neededReview monitoring reports and protocol deviations to identify site- and study-level trendsProactively develop study materials that aid the Clinical Affairs team and site. Mitigate risk by assisting in the improvement of current study documents.Travel to clinical sites at a minimum of an annual basis when remote monitoring option is not availableMaintain and grow collaborative relationships with all Discovery personnel Participate and take initiative in process improvement activities for departmentStay abreast of industry-accepted procedures and educate fellow team members of standards/policyCollaborate with team members to develop improved methods of tracking study informationMaintain accurate data in SalesForce database and utilize communication toolsRespect the privacy of the personal information of patients, co-workers, and all individuals with whom the company interacts Compensation and Benefits:Discovery Life Sciences is committed to fair and equitable compensation practices, and we strive to provide employees with total compensation packages that are market competitive. For this role, the anticipated base pay range is $50,000-$75,000. The exact base pay offered for this role will depend on various factors, including but not limited to the candidate's qualifications, skills, and experience. Your annual salary is only one part of your total compensation package. Other benefits:Competitive salary and benefits package options including medical, dental, vision, life, and disability which start on your first day of employment!401(k) match program which starts on your first day of employmentTime away from work (Generous vacation and paid time off, paid parental leave, paid family leave, etc.).Professional development opportunities and reimbursement for relevant certifications.Collaborative and inclusive work environment that values diversity.Team-building activities and social events.Employee Referral Program and Colleague Recognition Program Location, work hours, and application details:Remote - United StatesUp to 50% domestic travel for mandatory site meetings and trainingsMonday - Friday, start time between 7am and 9am local timeApplications for this position will be accepted until the role has been filled We are actively seeking motivated, dedicated individuals like you to join our thriving organization. As a leader in our industry, we offer unparalleled opportunities for professional growth and success.The Discovery Life Sciences Talent Acquisition team proudly manages and represents all Discovery recruitment activities. We respectfully request that third party staffing agencies refrain from submitting candidates or soliciting meetings to discuss recruiting services.We are unable to sponsor or take over sponsorships of any applicant work visas at this time. Apply Now to join our team! Visit dls.com/careers for more details. Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.