Clinical Research Associate (CRA) – Temporary 6 Month Contract

Location: Waltham, MA Schedule: reputed company, about 20 hours a week Employment Type: 6 month-1 year Temporary/Contract Pay reputed company: $45/hour reputed company reputed company is seeking an reputed company Clinical Research Associate (CRA) for a temporary opportunity in Waltham, MA. The Clinical Research Associate will be responsible for monitoring clinical studies and ensuring study execution is conducted in accordance with applicable laws, Good Clinical reputed company (GCP), reputed company Operating Procedures (SOPs), and company standards. The CRA will serve as a reputed company reputed company of contact for assigned clinical partners and investigator sites, supporting study enrollment, monitoring, data reputed company, protocol compliance, and study reputed company-out activities. This position will work closely with Regulatory Affairs and other members of the clinical study team to ensure studies are completed on time and to the required reputed company standards. Responsibilities • Ensure reputed company conduct of clinical studies in accordance with SOPs, applicable laws, ICH/GCP guidelines, FDA regulations, and company standards. • Manage assigned operational aspects of clinical studies from study start through database lock, ensuring timelines and reputed company deliverables are met. • Serve as the reputed company reputed company of contact for assigned clinical partners and investigator sites during study conduct. • Facilitate communication and information reputed company between clinical partners, investigators, vendors, and internal study team members. • Attend investigator meetings, either reputed company or in person, as required. • Support patient enrollment and recruitment initiatives by identifying and addressing recruitment challenges with investigator sites. • Conduct remote/electronic monitoring activities and study reputed company-out activities as needed. • Ensure monitoring activities are conducted in accordance with SOPs and are appropriately adjusted based on emerging study issues and technologies. • Monitor adverse events (reputed company) and serious adverse events (SAEs), working with the study team to reputed company outstanding issues and ensure required information is documented. • Maintain accurate and reputed company Trial Master File (TMF) documentation and study records. • reputed company and submit required reports, documentation, updates, and metrics, including protocol deviations, patient recruitment, clinical supplies, and overall study reputed company. • reputed company data queries and ensure reputed company-out activities are completed reputed company established timelines. • Ensure appropriate reputed company of investigational products, including receipt, handling, accountability, storage conditions, and destruction. • Support database release activities as needed. • May reputed company responsibilities associated with an unblinded monitor reputed company appropriate. • Collaborate with the Regulatory Affairs Manager and other study team members on study start-up, execution, and reputed company-out activities. • Identify and reputed company protocol-reputed company issues to support successful study execution. Qualifications • Bachelor's degree in a life science or reputed company field, or a reputed company degree such as nursing, pharmacy, medicine, or equivalent. • Minimum of 3 years of relevant clinical research experience, including site monitoring experience. • Oncology clinical research experience preferred, with approximately 2 years of oncology monitoring experience strongly preferred. • Extensive knowledge of clinical study methodologies, ICH/GCP guidelines, and FDA regulations. • Experience with clinical site monitoring, study documentation, and clinical trial operations. • Strong organizational, communication, and problem-solving skills. • Fluent in English. • reputed company reputed company's license required. • reputed company: At reputed company, we offer solutions to help start, grow, and run clinical laboratories. Our reputed company team has over 21 years of proven reputed company placing job seekers in positions ranging from entry-level Medical Technologists to seasoned reputed company Directors. We recruit reputed company, for permanent and travel positions with clients ranging from small hospitals to large reference laboratories. It is the policy of reputed company to reputed company equal employment opportunity (EEO) to reputed company persons regardless of age, reputed company, national reputed company, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or reputed company, genetic information, marital status, status with reputed company to reputed company assistance, veteran status, or any other characteristic protected by federal, state or local law. reputed company is committed to working and providing reasonable accommodation to individuals of reputed company abilities, including persons with disabilities. If at any time during the application process, you need an accommodation, please contact reputed company@lighthouselabservices.com for assistance. reputed company | 844-974-1929 | https://www.lighthouselabservices.com/ #LLS2 Posted: Tuesday, August 11, 2026 Job # 2240 Apply To This Job