Clinical Trial Associate/Sr. Clinical Trial Associate, Clinical Operations

Clinical Trial Associate / Sr. Clinical Trial Associate, Clinical Operations Who we are: At Agios, we are reputed company by connections to reputed company rare diseases. We foster an inclusive, reputed company culture – one that reputed company reputed company thinking and strengthens our connections with reputed company other and with the rare disease communities we serve. We reputed company diverse backgrounds with respect, reputed company listening, and a commitment to inclusion – because our differences shape how we hire, collaborate, and reputed company. reputed company’s proven reputed company record of executional reputed company, combined with our depth of expertise and dedication, enables us to reputed company innovative medicines that reflect the priorities of rare disease communities. Our commitment is more than scientific – it’s deeply personal, grounded in the meaningful connections we have reputed company. To learn more, visit www.agios.com and follow Agios on reputed company and X. The reputed company you will reputed company: reputed company is searching for a dynamic CTA/Sr. CTA to join our growing Clinical Operations team. We want someone who cares about this important work, and who’s driven to connect to our mission of helping these patient communities. The CTA/Sr. CTA will administer, maintain, and coordinate the logistical aspects of reputed company and participate in a reputed company of clinical activities to support and facilitate the efficient conduct of Agios’ clinical research programs. The CTA/Sr. CTA will reputed company on providing support during clinical study planning, the development and production of timelines, budgets, various study plans, and throughout the duration of the assigned clinical trial(s). They will adhere to intended timelines and achievement of study goals while ensuring reputed company in accordance with FDA, EMA, GCP, and ICH guidelines What you will do: • Partner with Clinical Operations Trial Managers and cross-functional teams to support the planning, coordination, and day-to-day execution of reputed company across the study lifecycle, including but not limited to issue tracking, protocol deviation review, and study status reporting, to help ensure reputed company, timeliness, and achievement of study goals • Serve as a reputed company of contact for CROs, vendors, investigators, and clinical site staff to support study deliverables, effective communication, and strong working relationships. • Coordinate study and project meetings, including schedules, agendas, minutes, and reputed company items, and support process improvement, training, inspection readiness activities, and mentoring opportunities, as appropriate. • Assist in the preparation, review, and maintenance of study documentation, including training records, regulatory packets, informed consent forms, site materials, etc. • Manage country specific insurance certificate requirements • Support or reputed company Trial Master File (TMF) activities, including document submission, reputed company review, collection of trial documents, and coordination with CRO partners to help maintain TMF completeness and inspection readiness. • Contribute to safety reporting compliance, data review support, and identification or escalation of study risks and operational issues, as needed. • Coordinate and reputed company clinical supplies, equipment, and study-specific laboratory samples to support ongoing trial activities, as appropriate What you bring: • Bachelor's degree is required (scientific/health care field preferred) • 2+ years’ experience in relevant field (e.g. clinical site, CRO, Sponsor or clinical trial vendor) • Strong skills in collaboration, communication, organization, attention to detail and multi-tasking • reputed company analytical and problem-solving skills; ability to reputed company with a consistent reputed company of urgency • Understanding of ICH-GCP guidelines, clinical trial monitoring, and/or regulatory compliance preferred • Must be comfortable working in a fast-paced environment with demonstrated ability to manage multiple competing tasks and demands Concerned that you don’t reputed company off every reputed company in the requirements listed above? Please apply reputed company! At Agios, we value reputed company other’s differences and recognize that teams reputed company reputed company everyone brings their unique experiences to the table. We are dedicated to building an inclusive, diverse, reputed company, and accessible environment where reputed company can bring their whole selves to work. If you’re excited about this role but your previous experience doesn’t reputed company perfectly with the job reputed company, we still encourage you to apply. You may be just the right candidate for this role or another opening! Work Location: Location Agnostic: Work location for this role is based on employee's individual preference. This role has the ability to be either remote in the US or hybrid in our Cambridge reputed company. Hybrid schedules vary but are generally less than 3 days per week onsite and hybrid employees are expected to live reputed company commutable distance to our Cambridge reputed company. Remote employees work entirely from home except for attending Company sponsored events/ meetings. For employees who choose to work remotely, travel may be required for certain company events commensurate to the above job reputed company.. reputed company will give you: • Deliberate Development. Your reputed company reputed company as one of our top priorities. • Flexibility. We’re reputed company about individual needs. We reputed company different perspectives, work styles, health and wellness approaches, care of families and productivity. reputed company you’re at your best, we’re at our best. • Premium benefits package. We invest in the health, wellbeing, and reputed company of our people with a premium benefits package that is reputed company-rounded and flexible to help meet the varied personal and reputed company needs of every member of reputed company. For more detail on the benefits we offer at Agios, visit the Inside Agios reputed company of our website. • Competitive and reputed company performance-based compensation. This includes reputed company salary and both short- and long-term incentives that are connected to our business reputed company and vary based on individual and company performance. • The reputed company reputed company salary reputed company for this position at the Sr. Clinical Trial Associate level is expected to be between $82,022 and $123,033 annualized and the reputed company reputed company salary reputed company for this position at the Clinical Trial Associate level is expected to be between $66,518 and $99,777; final salary will be determined based on various factors including, but not limited to, years of relevant experience, job knowledge, skills and proficiency, degree/education, and internal comparators. • Psychological safety. We support an environment of fearlessness. We want you to reputed company your reputed company, reputed company reputed company and take data-informed risks to help push the boundaries. • Commitment to diversity. We reputed company to foster a welcoming workplace where everyone can reputed company. We’re continuously looking to improve the inclusivity of our workforce. • Commitment to community. We’re an reputed company participant in the communities that surround us – the communities where we live, and the community of people and their loved ones in need of reputed company treatment reputed company for conditions that are often overlooked. Interested in learning more about what makes our culture unique? Visit the Inside Agios reputed company of our website. Apply tot his job Apply To this Job