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Senior Clinical Trial Manager

Employer
Alumis Inc.
Location
South San Francisco, California
Start date
May 29, 2024

View more

Discipline
Clinical, Clinical Research, Clinical Trials
Required Education
Bachelors Degree
Position Type
Full time
Hotbed
Biotech Bay

Job Details

Alumis Inc. is a precision medicines company with the mission to transform the lives of patients with autoimmune diseases. Even with treatment innovations of the last two decades, many patients with immunologic conditions continue to suffer - our goal is to fundamentally change the outcomes for these patients.


As a Senior Clinical Trial Manager at Alumis, you will be responsible for executing clinical studies to the highest quality standards. You will ensure the integrity of clinical data, adhere to schedules, and manage budgets for Phase I-IV clinical trials by overseeing and managing vendors and contractors. By embracing our core values—We Elevate, We Challenge, We Nurture—you will play a pivotal role in driving the success of our clinical programs and advancing innovative treatments.


 

Essential Responsibilities

  • Manage all day-to-day execution of global clinical studies on one or more clinical programs from initial study synopsis through final project deliverables (study set-up, enrollment, conduct, database lock, final TLFs, CSR, etc.).  May sit on the Clinical Development Team (if functioning as a study lead). 
  • Oversee aspects of clinical trials from start-up through completion 
  • Facilitate the development and review of protocols, informed consent documents, and clinical sections of Investigator Brochures. 
  • Conduct vendor feasibility, capabilities, selection, management, and oversight activities. 
  • Ensure on-time execution and conduct of clinical studies, including tracking the development of budget items, milestones, and timelines. 
  • Coordinate cross-functional study team members (e.g. biostats, contracts, quality assurance, regulatory, clinical pharmacology, data management, medical monitors) and stakeholders (study vendors) to ensure initiation and execution of clinical study deliverables within approved budget and timelines. 
  • Manage risk and mitigation, prioritizing competing tasks and issues to ensure program/study objectives are successfully accomplished. 
  • Contribute to or lead the systems set-up/management including EDC, IRT, Central Laboratories, specialty services (ePRO, eDiary, etc.).  
  • Ensure data integrity through routine data reviews, query resolution, and consistency checks. 
  • Critically assess data to detect trends, outliers, and responsively direct resources and attention to correct problems early.  
  • Track and communicate program/study progress to Senior Management, creating and updating detailed dashboards, trackers and presentation materials. 
  • Ensure timely submission of documents to TMF and provide oversight to ensure TMF completeness and quality. 


Professional Experience / Qualifications: 

  • Demonstrated experience in initiating and managing Phase I-IV clinical trials. 
  • Proven experience in managing CROs and selecting vendors. 
  • Willingness to be hands-on and perform tasks within tight turnaround times. 
  • Excellent interpersonal and communication skills with developing leadership attributes. 
  • Success working in a matrixed environment. 
  • Experience in the application of US and Global Regulations and Guidance (SOPs, ICH-GCP, FDA-CFR, ethical standards). 
  • Expertise in data collection, monitoring, cleaning, and analysis throughout clinical development (Phase I-IV). 
  • Ability to multitask in a fast-paced environment. 
  • Strong ability to build cooperative relationships with coworkers. 
  • Capable of authoring complex documentation with minimal supervision. 
  • High degree of attention to detail. 
  • Comfortable with travel and able to travel up to 25% of the time as needed. 

 

Preferred Education

B.S. or advanced degree in biological sciences or a related discipline.


Preferred Experience

At least 8 years of relevant experience, including previous experience managing clinical trials at a biopharma company or a Contract Research Organization (CRO).


Preferred Computer Skills

Proficiency in Microsoft Office (Word, Excel, Outlook), Smartsheet, electronic TMF, and electronic clinical technologies.

 

Alumis Values


  • Elevate
  • Challenge
  • Nurture

 

This position is located in South San Francisco, CA, with the expectation of being in the office 3 days a week, Tuesday through Thursday. At this time we are not considering remote applicants.

 

The salary range for this position is $ 185,000 USD to $195,000 USD annually. This salary range is an estimate, and the actual salary may very based on the Company’s compensation practices.

 

Alumis Inc. is an equal opportunity employer. 

Company

Alumis Inc. is a precision medicines company with the mission to transform the lives of patients with autoimmune diseases. Our experienced leadership team brings a proven track record in precision drug development of groundbreaking therapies.

Even with treatment innovations of the last two decades, many patients with immunologic conditions continue to suffer.

With a unique precision analytics platform and an unwavering commitment to advancing our understanding of immunologic diseases, Alumis Inc. will rewrite the autoimmune treatment playbook by developing the right medicine for each patient.
 

Company info
Website
Location
611 Gateway Blvd
Suite 820
South San Francisco
California
94080
US

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