Senior Clinical Project Associate
Relay Therapeutics is hiring a Senior Clinical Project Associate in Cambridge, United States. It pays $69k-$99k a year and Level rates it ; you can apply on Level.
Level's read on this job
- Little AI ●○○○ is how Level rates this role: aI is not part of the work.
- Tools and skills the posting cites include Ms Office, Ms Project and Excel.
- Level files it as a senior role.
- Level lists 15 other open roles at Relay Therapeutics.
- The role was posted in the last few days.
AI in this role
Coordinate clinical trial execution, study start-up, and regulatory compliance as a Senior Clinical Project Associate.
The Opportunity:
As Senior Clinical Project Associate, you will be accountable for providing clinical trial coordination
support, along with implementing operational plans in accordance with regulatory guidelines and
ICH/GCP standards. You will be an integrated member of the Relay Tx Clinical Development Operations
team making key contributions to the execution of clinical trials that will translate Relay’s innovative
science into impactful medicines for patients.
Your Role:
- You will support the day-to-day operations of clinical trial execution, with a focus on site start-up,
study participant enrollment, clinical monitoring, drug supply planning, defining clinical supply
logistics, GCP and protocol compliance, from the clinical sites, CROs and vendors. - You will coordinate with the CRO and the Relay Tx Clinical Operations Lead to support planning from
study initiation through study closure. - You will maintain study trackers and provide metrics as needed.
- You will review and contribute to key study documents including, but not limited to, informed
consent forms, case report forms, and study plans. - You will assist with the preparation and distribution of meeting agendas and minutes as well as
actively participate in team meetings providing updates on your key responsibilities. - You will help to ensure the Trial Master File is up-to-date and inspection ready.
- You will support inspection readiness by collaborating with CROs and providing support to clinical
sites to prepare for and respond to audit/inspection findings conducted by internal QA and external
regulatory agencies. - You will actively participate in the development of department initiatives; contribute ideas to
department initiatives that will make a difference to the efficiency and effectiveness of Clinical
Operations.
Your Background:
- You have 2-3 years of experience in clinical trial experience. CRO or Sponsor experience is strongly
preferred. - You are familiar with GCP and ICH Guidelines and the application to the conduct of clinical trials
- You are a motivated self-starter who is capable of flourishing in a fast-paced small company
environment. - You are a creative problem-solver with excellent communication and public speaking skills.
- You are familiar with MS Office products (MS Project, Excel and Power Point)
- You have strong interpersonal and organizational skills, with a high degree of attention to detail.
- You are pragmatic and able to manage multiple projects and needs effectively
Estimated Salary Range: [$69,000 - $99,000].
The range provided above is based on what we believe to be a reasonable estimate for this job at the time of posting. Actual base salary will depend on a number of factors, including but not limited to, a candidate’s education, experience, skills and location.
#BP1
About Relay Therapeutics
Relay Therapeutics is a clinical-stage precision medicines company transforming the drug discovery process with the goal of bringing life-changing therapies to patients. Built on unparalleled insights into protein motion and how this dynamic behavior relates to protein function, we aim to effectively drug protein targets that have previously been intractable, with an initial focus on enhancing small molecule therapeutic discovery in targeted oncology. Our Dynamo platform integrates an array of leading-edge experimental and computational approaches to provide a differentiated understanding of protein structure and motion to drug these targets. We have built a world-class team of leading experts from each of these disciplines, and they are driven by a deep collaboration at every step of our drug discovery process.
Our team is equal parts fearless and relentless, with a shared passion for working collaboratively in intellectually stimulating environments. If you’re excited by the challenge of putting protein motion at the heart of drug discovery and passionate about making a difference in the lives of patients, join us!
How we rate this
Senior Clinical Project Associate at Relay Therapeutics rates 0 out of 100 for how much of the daily work is AI. That makes it Little AI (AI Level 1 of 4). The level is about AI in the job, not seniority.
Little AI. AI is not part of the work.
- ●●●● Builds AI80 to 100
- ●●●○ Works on AI60 to 79
- ●●○○ Uses AI40 to 59
- ●○○○ Little AI0 to 39
Levels come from how often the tools, models and workflows of the role are named in the posting itself. Open the description and count.
Prepare for this job
Built from this posting and from similar jobs on Level.
Skills and AI tools this role asks for
Questions you could be asked
- Tell me about a project where clinical operations was part of your work. What did you do?
- Tell me about a project where clinical trials was part of your work. What did you do?
- Tell me about a project where google cloud was part of your work. What did you do?
- Tell me about a project where compliance was part of your work. What did you do?
- Walk me through how you've used Ms Office in your day-to-day work.
Adapt your resume
- List these exact terms on your resume: Clinical Operations, Clinical Trials, Google Cloud, Compliance, and Ms Office. An applicant tracking system matches the wording, not the idea.
- Attach one line of real, concrete experience to at least one of them. A tool named with nothing behind it rarely survives a human read.
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