What are the responsibilities and job description for the Senior Clinical Trial Specialist position at Alector?
At Alector, our mission is to develop therapies that empower the immune system to combat neurodegeneration. Our team is solely focused on developing treatments for some of the most challenging diseases facing our society. We are supported in this mission by experienced and accomplished scientists and clinicians, leading healthcare investors, and pharma company partners who share in our commitment to bettering the lives of patients.
Would you like to take part in developing new therapies that really make a difference in patients' lives? Do you desire both autonomy and collaboration in taking on scientific challenges that interest you? Are you interested in joining a talented team where everyone has a voice?
The Senior Clinical Trial Specialist (Sr. CTS), works closely with the Clinical Operations team to support clinical trial execution. Key accountabilities include the coordination of activities associated with the start-up and management of a clinical trial in compliance with SOPs, regulations, and ICH/GCP guidelines. The Sr. CTS interacts with the program and study trial managers, Director of Clinical Operations, Regulatory, and other key functions both internally and externally to support activities and project deliverables within the required time frame and budget.
At Alector, we believe that hard-working teams include people from a wide variety of backgrounds and experiences who can challenge each other’s assumptions with fresh perspectives and bring creative ideas to the table. We are committed to building an open, diverse, and inclusive environment for all employees. We do not discriminate on the basis of race, religion, color, national origin, sex, gender, sexual orientation, age, marital status, veteran status, or disability status, or any other characteristics protected under applicable federal, state, or local laws.
Alector is a phenomenal place to learn and experiment. If you excel in a dynamic environment where everyone is committed to finding a treatment, where you’ll drive growth, this is the role for you. There is no limit to how far you can go with us.
Benefits
While we’ve focused on what to look forward to during the first year and beyond, Day One is great, too: committed and driven colleagues, a bold and important company goal, brand-new brightly-lit offices in the heart of the biotech area, competitive compensation and benefits. But these matter only if you’re excited to build and own something great, and tackle these challenges with us. Come join us.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
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