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New · posted Oct 31

Tango Therapeutics · Biotechnology

Senior Clinical Data Manager

  • Boston, MA
  • Hybrid
  • Full-time
  • Manager
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EmploymentFull-time
DeadlineOpen until filled

The role

The Senior Manager, Clinical Data Management serves as the Data Management lead for assigned clinical trials and is responsible for the planning, oversight, execution, and delivery of data management activities from study startup through database lock and study closeout. The role provides sponsor oversight of outsourced data management activities, ensures high-quality and inspection-ready clinical data, and collaborates with cross-functional stakeholders to support trial execution, regulatory compliance, and clinical development objectives.

What you need

What You Bring

  • Bachelor's degree in Computer Science, Life Sciences, Mathematics, Health Sciences, or related field
  • 5+ years of Clinical Data Management experience within the biotechnology, pharmaceutical, or CRO industry
  • Experience leading Data Management activities for clinical trials in a regulated environment
  • Experience managing outsourced Data Management activities and providing vendor oversight
  • Experience managing clinical systems (incl. IRT/ eCOA) configurations and implementations, enhancements, integrations, and technology vendors;
  • Experience leading User Acceptance Testing (UAT)
  • Experience supporting database build, data cleaning, external data integrations, medical coding, database lock, and submission readiness activities
  • Experience working within global clinical development organizations
  • Experience supporting audits, inspections, and inspection-readiness activities preferred
  • Experience using electronic data capture (EDC) platforms and clinical data technologies
  • Oncology clinical development experience preferred
  • Strong knowledge of Clinical Data Management processes and the clinical trial data lifecycle
  • Strong knowledge of ICH-GCP, FDA regulations, EU Clinical Trial Regulation (CTR), data integrity principles, and other applicable regulatory requirements
  • Knowledge of CDISC standards, including CDASH and SDTM, and associated clinical data requirements
  • Proficiency with EDC systems, IRT, eCOA, and related clinical technologies
  • Knowledge of medical coding dictionaries, including MedDRA and WHODrug
  • Familiarity with data visualization, analytics, and reporting tools
  • Strong understanding of risk-based quality management and critical-to-quality (CtQ) principles
  • Strong vendor management and sponsor oversight capabilities
  • Strong project management, organizational, and prioritization skills
  • Excellent collaboration skills with cross-functional stakeholders, including Biostatistics, Statistical Programming, Pharmacovigilance, Clinical Operations, and Regulatory Affairs
  • Strong analytical thinking, problem-solving, and decision-making capabilities
  • Excellent written and verbal communication skills

We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

What you'll do

Your Role

  • Serve as the Data Management representative within the Clinical Trial Team (CTT) and provide oversight of Data Management activities throughout the clinical trial lifecycle
  • Provide sponsor oversight of CRO and external data vendors, ensuring Data Management, IRT and eCOA activities and deliverables are executed in accordance with study requirements, quality standards, timelines, budgets, contractual obligations, and regulatory requirements
  • Ensure timely delivery of complete, accurate, reliable, and inspection-ready clinical data through effective oversight of outsourced Data Management activities, including EDC, IRT and eCOA system build, validation and maintenance, data collection, data cleaning, medical coding, external data integration and reconciliation, database/system lock, and submission readiness
  • Review and approve key Data Management deliverables, including CRF/eCRF, IRT, eCOA specifications, edit checks, Data Management Plans, CRF completion guidelines, data transfer specifications, external data reconciliation plans, and other study-specific documentation
  • Establish and monitor data quality metrics, KPIs, and data review strategies to ensure data integrity, consistency, and compliance throughout the study lifecycle
  • Lead oversight of external data integrations, transfers, reconciliations, and vendor-managed data streams to ensure completeness, quality, and regulatory compliance
  • Partner with CTT, CRO and external vendors to support effective planning, integration, review, and reporting of clinical trial data
  • Identify data-related risks and issues and lead the development, implementation, and monitoring of mitigation and contingency plans
  • Participate in audits, inspections, and inspection readiness activities and ensure timely assessment, response, and resolution of Data Management-related findings
  • Contribute to regulatory submissions, health authority responses, and other regulatory deliverables, as required
  • Support the development and implementation of Data Management standards, processes, technologies, and continuous improvement initiatives

Pay

$144,800 – $217,200 a year

Employer provided
How this compares

$144,800—$217,200 USD

Where you'll work

Boston, MAHybridOpen in Maps (opens in a new tab)

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From the posting

About Tango Therapeutics

Tango Therapeutics is a biotechnology company dedicated to discovering novel drug targets and delivering the next generation of precision medicine for the treatment of cancer.

Using an approach that starts and ends with patients, Tango leverages the genetic principle of synthetic lethality to discover and develop therapies that take aim at critical targets in cancer.

This includes expanding the universe of precision oncology targets into novel areas such as tumor suppressor gene loss and their contribution to the ability of cancer cells to evade immune cell killing.

Tango’s labs and offices are located at 201 Brookline Avenue, in the vibrant Fenway area of Boston, Massachusetts.

Tango Therapeutics company page · 7 open roles
Equal opportunity, accessibility and legal noticesTango Therapeutics's statements, word for word

We are an equal opportunity employer and value diversity at our company.

Job intelligence

The context around this role

Live data · October 31, 2026

Salary intelligence

How the pay compares

This role's midpoint is level with the US median for Clinical Data Management roles at this level.

This roleEmployer provided

$144,800 to $217,200 a year

Manager roles in the US11 roles publishing pay

Middle half $164,500 to $181,000, median $181,000
Annual base pay
Annual base payLowMedianHigh
This role$144,800—$217,200
All US$164,500$181,000$181,000

This role: Tango Therapeutics's own published range. Comparisons: the base pay employers published on open Clinical Data Management roles at the same level on Regulatory Jobs, October 31, 2026. Nothing is estimated.

Career trajectory

Where this role sits in Clinical Data Management

The general path across 29 open Clinical Data Management roles on Regulatory Jobs, with the titles they carry most. Not Tango Therapeutics's own promotion track.

  1. Earlier

    Associate & Specialist

    Often: Associate, Clinical Data Systems · Clinical Data Associate

  2. One step back

    Senior & Principal

    Often: Clinical Data Manager · eCOA

    $148K median8 open
  3. This role

    Manager

    Often: Senior Manager, Clinical Data Systems · Senior Manager, Clinical Data Management

    $181K median13 open
  4. Next step

    Director

    Often: Associate Director, Clinical Data Management · Director, Clinical Data Management

    $196K median6 open

Skills DNA

What this role leans on

How many of the posting's 36 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

GMP and compliance: 7 linesLab testing and methods: 2 linesDocumentation and SOPs: 2 linesValidation and qualification: 1 lineRegulatory submissions: 3 linesQuality systems and risk: 2 linesData and digital systems: 14 linesClinical trial conduct: 14 linesCollaboration and leadership: 6 linesGMPLab testingDocumentationValidationSubmissionsQuality systemsData systemsClinical trialsTeamwork
  • Data and digital systems14
  • Clinical trial conduct14
  • GMP and compliance7
  • Collaboration and leadership6
  • Regulatory submissions3
  • Lab testing and methods2
  • Documentation and SOPs2
  • Quality systems and risk2
  • Validation and qualification1

Company hiring pulse

Tango Therapeutics on Regulatory Jobs

7
Open roles
7
Distinct roles
1
Locations

By discipline

  • Clinical4 57%
  • Quality3 43%

By level

  • Director4 57%
  • Manager2 29%
  • Senior & Principal1 14%
See all 7 Tango Therapeutics roles

More roles at Tango Therapeutics

All 7 Tango Therapeutics roles

Similar Clinical Data Management roles elsewhere

Senior Clinical Data Manager at Tango Therapeutics

Open until filled. $145K–$217K a year, employer provided.

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