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Pharmapace, Inc.
Home
About Us
  • Leadership
  • Core Business
  • Therapeutic Experience
  • How We Manage Your Data
  • Privacy Cookie Statement
Services
  • Biostatistics
  • Data Management
  • Statistical Programming
  • CDISC (SDTM/ADaM)
  • Regulatory Submissions
  • Clinical Data Integration
  • ClinicalTrials.gov Submit
  • Medical Writing
  • FSP
  • BIMO
  • PK/PD Analysis
  • Project Management
Contact Us
Careers
  • Open Positions
News
  • Publications
  • Events & Impact
More
  • Home
  • About Us
    • Leadership
    • Core Business
    • Therapeutic Experience
    • How We Manage Your Data
    • Privacy Cookie Statement
  • Services
    • Biostatistics
    • Data Management
    • Statistical Programming
    • CDISC (SDTM/ADaM)
    • Regulatory Submissions
    • Clinical Data Integration
    • ClinicalTrials.gov Submit
    • Medical Writing
    • FSP
    • BIMO
    • PK/PD Analysis
    • Project Management
  • Contact Us
  • Careers
    • Open Positions
  • News
    • Publications
    • Events & Impact
  • Home
  • About Us
    • Leadership
    • Core Business
    • Therapeutic Experience
    • How We Manage Your Data
    • Privacy Cookie Statement
  • Services
    • Biostatistics
    • Data Management
    • Statistical Programming
    • CDISC (SDTM/ADaM)
    • Regulatory Submissions
    • Clinical Data Integration
    • ClinicalTrials.gov Submit
    • Medical Writing
    • FSP
    • BIMO
    • PK/PD Analysis
    • Project Management
  • Contact Us
  • Careers
    • Open Positions
  • News
    • Publications
    • Events & Impact

Clinical Data Manager II

About the job

Pharmapace welcomes qualified and motivated candidates to apply for  Clinical Data Manager II. Pharmapace is a fast growing and specialized consulting/outsourcing company serving the biotech and pharmaceutical companies in their clinical development programs. We offer a stimulating working environment and excellent career growth opportunity.


 Key Responsibilities

 

  • Lead and oversee all data management activities for assigned studies, ensuring compliance with GCP, ICH, and company standards.
  • Serve as the primary contact for sponsors, vendors, and sites on all data-related matters.
  • Manage database setup, design, and validation, including CRF/eCRF design, annotation, database specifications, and validation testing.
  • Oversee data integrity and quality through query management, data listings review, and discrepancy resolution.
  • Perform data management closeout activities including SAE reconciliation, medical coding, and database quality control through database lock.
  • Support and/or lead internal and sponsor meetings, providing clear updates and technical guidance on data management deliverables.
  • Contribute to business development activities, including participation in client meetings and proposal discussions.
  • Train and mentor junior data management staff, supporting their technical and professional growth.
  • Ensure adherence to project timelines, deliverables, and budget constraints, escalating risks or issues proactively.
  • Maintain proper study documentation and ensure compliance with trial master file requirements.
  • Contribute to process improvement initiatives and share best practices across the department.

 


Qualifications:

Education & Experience:

  • Associate’s degree with a minimum of 4 years of data management lead experience, or equivalent 4–6 years of industry experience.
  • BS/MS in Life Sciences or technical discipline with at least 3 years of data management lead experience preferred.
  • Proven experience managing moderate to complex projects across both paper and EDC studies; global project experience preferred.
  • Solid understanding of FDA, ICH, GCP, NDA, IND, and other regulatory guidelines.
     

Skills & Competencies:

  • Strong knowledge of clinical data management principles and systems.
  • Excellent oral and written communication skills with the ability to build rapport with sponsors, sites, and vendors.
  • Strong analytical, organizational, and problem-solving skills with high attention to detail.
  • Proven ability to lead data management tasks independently with minimal supervision.
  • Proficiency in Microsoft Office Suite; familiarity with SAS or other programming tools a plus.
  • Ability to manage multiple priorities, work effectively in a team environment, and mentor junior colleagues.
  • Professional demeanor, proactive mindset, and commitment to quality and accuracy.


Pharmapace offers competitive salaries plus stock options, 401K plan with company match, health/dental/vision insurances, and holiday/vacation benefits.  Pharmapace is an equal opportunity employer. We prohibit unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin/ancestry, age, disability, marital status, and veteran status.


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Pharmapace, Inc. 

10509 Vista Sorrento Pkwy, Ste 303, San Diego, CA 92121

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