New · posted Nov 10
Relay Therapeutics · Biotechnology
Associate Director, Clinical Data Management
- Cambridge, MA
- On-site
- Full-time
- Director
The role
As Associate Director, Data Management, you will be accountable for delivery, integrity, and quality of Relay’s clinical data across the clinical studies. You will be an integrated member of the Relay Tx Clinical Data Management Team, responsible for the in-house data management expertise for the execution of clinical studies that will translate Relay’s innovative science into impactful medicines for patients. You will report to the Executive Director, Clinical Data Management.
What you need
What you'll do
Your Role
- You will be responsible for oversight and execution of data management activities for the assigned clinical study including data timelines and key deliverables.
- You will work directly with and oversee CROs and vendors for outsourced Data Management activities. Is responsible for CRO performance and data management metrics for assigned programs.
- You will lead database development and eCRF design, UAT, data import specifications, Case Report Form completion guidelines, data entry guidelines and related operations manuals.
- You will lead data validation specifications and programs for assuring the accuracy of clinical trial data, e.g., manual data review guidelines, computerized edit check programs, Data Management Plans (DMP).
- You will be responsible for executing or overseeing data cleaning activities through to database lock: includes generating and managing clinical trial data queries, data review listings, reconciling serious adverse events, coding, central and local lab data, and external data.
- You will collaborate with a dynamic Relay cross-functional team to ensure timeliness and quality of data deliverables.
- You will ensure compliance with global regulatory requirements and quality standards.
- You will contribute to data standards including CRF and participate in data system development initiatives and database integration projects.
- You will participate in SOP development, training of junior data managers, process mapping, and other departmental activities.
Pay
$147,000 – $210,000 a year
Employer providedYour Background
- You should ideally have 7+ years of experience in the pharmaceutical / biotechnology industry as a Data Manager. Sponsor experience is strongly preferred.
- You have advanced experience with data collection and cleaning covering Phase I, II and III studies. Oncology experience is preferred.
- You have experience in executing clinical studies across various phases is desirable. Expertise in oncology drug development is preferred.
- You have a strong and current knowledge in global regulatory and compliance requirements including but not limited to US CFR, EU CTD, ICH GCP, and CDISC.
- You have experience in CRO and vendor oversight.
- You are a motivated self-starter who is capable of flourishing in a fast-paced small company environment and able to work independently.
- You are a creative problem-solver with excellent communication and public speaking skills.
- 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: [$147,000 - $210,000].
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.
Where you'll work
Cambridge, MAOn-siteOpen in Maps (opens in a new tab)
More jobs in Cambridge, MA
From the posting
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!
Job intelligence
The context around this role
Live data · November 10, 2026
Salary intelligence
How the pay compares
This role's midpoint is 20% below the US median for Clinical Data Management roles at this level.
This roleEmployer provided
Director roles in the US13 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $147,000 | — | $210,000 |
| All US (middle half) | $196,000 | $223,000 | $244,000 |
This role: Relay Therapeutics's own published range. Comparisons: the base pay employers published on open Clinical Data Management roles at the same level on Regulatory Jobs, November 10, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Clinical Data Management
The general path across 63 open Clinical Data Management roles on Regulatory Jobs, with the titles they carry most. Not Relay Therapeutics's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 10 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Documentation and SOPs5
- Data and digital systems5
- Clinical trial conduct5
- Collaboration and leadership5
- GMP and compliance1
- Validation and qualification1
Regulatory intelligence
The rules, regulations and standards behind this role
The regulations, guidance and standards that govern Clinical Data Management work in biotechnology, each linked to the agency or standards body that publishes it.
- CDISCCDISC standards(official source, opens in a new tab)SDTM, ADaM and CDASH, the clinical data standards FDA and PMDA require
- FDAFDA study data standards(official source, opens in a new tab)Required data standards and technical conformance for clinical study data
- ICHICH E6(R3) good clinical practice(official source, opens in a new tab)The international standard for the design, conduct and reporting of clinical trials
- FDA21 CFR Part 11(official source, opens in a new tab)FDA rules for electronic records and electronic signatures
- ICHICH E9 and E9(R1)(official source, opens in a new tab)Statistical principles for clinical trials and estimands
- ICHMedDRA(official source, opens in a new tab)The ICH medical terminology for coding adverse events and medical history
- HHSHIPAA Privacy Rule(official source, opens in a new tab)Federal protections for individually identifiable health information
- EUGDPR (Regulation 2016/679)(official source, opens in a new tab)The EU General Data Protection Regulation for personal data, including health data
- FDA21 CFR Part 312(official source, opens in a new tab)Investigational New Drug applications and sponsor duties in drug trials
- EUEU Clinical Trials Regulation 536/2014(official source, opens in a new tab)How clinical trials of medicines are authorized and run in the EU, through CTIS
- FDA21 CFR Part 50(official source, opens in a new tab)Protection of human subjects: informed consent in FDA-regulated trials
- NIH42 CFR Part 11(official source, opens in a new tab)Clinical trial registration and results reporting on ClinicalTrials.gov
- FDAFDA Bioresearch Monitoring (BIMO)(official source, opens in a new tab)FDA inspections of clinical investigators, sponsors, IRBs and GLP labs
- ICHICH E3(official source, opens in a new tab)Structure and content of clinical study reports
- ICHICH E2A to E2F(official source, opens in a new tab)Clinical safety data management, expedited reporting and periodic safety reports
- FDAFDA Electronic Submissions Gateway(official source, opens in a new tab)The agency-wide gateway for receiving electronic regulatory submissions
Company hiring pulse
Relay Therapeutics on Regulatory Jobs
- 4
- Open roles
- 4
- Distinct roles
- 1
- Locations
By discipline
- Regulatory2 50%
- Clinical2 50%
By level
- Director4 100%
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Associate Director, Clinical Data Management at Relay Therapeutics
Open until filled. $147K–$210K a year, employer provided.