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Senior Clinical Data Manager

Remote: 
Full Remote
Salary: 
85 - 142K yearly
Experience: 
Senior (5-10 years)
Work from: 
California (USA), United States

Offer summary

Qualifications:

Bachelor’s Degree preferred, Minimum of 5 years experience in Clinical Data Management, including 2 years as Study Lead Data Manager., Experience with Electronic Data Capture (EDC) systems..

Key responsabilities:

  • Lead data management within study team
  • Manage ongoing data activities and oversee external data providers
  • Participate in data management trainings and industry standard implementation
  • Address operational issues, assist in department initiatives, and perform other relevant tasks
  • Travel approximately 10-20% domestic and international
Ionis Pharmaceuticals, Inc. logo
Ionis Pharmaceuticals, Inc. Research SME http://www.ionispharma.com/
501 - 1000 Employees
See more Ionis Pharmaceuticals, Inc. offers

Job description

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Your missions

Headquartered in Carlsbad, California, and with offices in Boston, Massachusetts, and Dublin, Ireland, Ionis has been at work for more than three decades discovering medical breakthroughs that have redefined life for people with serious diseases. We are pioneers in RNA-targeted medicines, and our platform continues to revolutionize drug discovery and transform lives for patients with unmet needs.  With five currently marketed medicines for serious diseases and an expansive late-stage pipeline, we continue to build upon our groundbreaking innovations in science and technology to provide greater value to patients; and we are well positioned financially to deliver on our strategic goals.

At Ionis, we pride ourselves on cultivating a challenging, motivating and rewarding environment that fosters innovation and scientific excellence. We know our success is a direct result of the exceptional talent and dedication of our employees.

With an unprecedented opportunity to change the course of human health, we look to add diverse individuals, skill sets and perspectives to our exceptional team. We continue to invest time, money, and energy into making our onsite and remote work environments a place where solid and lasting relationships are built and where our culture and employees can thrive.

We are building on our rich history, and believe our greatest achievements are ahead of us.  We invite you to apply and join us if you’re passionate about the opportunity to have meaningful impact on patients in need, our employees, and our organization.  Experience and contribute to our unique culture while you develop and expand your career!

 SENIOR CLINICAL DATA MANAGER

SUMMARY

The Senior Clinical Data Manager is responsible for all aspects of clinical database design and reporting. The Senior Clinical Data Manager executes on policies and procedures for gathering, analyzing, and reporting clinical data for clinical trials that are conducted in compliance with Good Clinical Practice (GCP) and regulatory requirements.

RESPONSIBILITIES

  • Acts as lead data manager within study team
  • Performs/oversees database development and management (e.g., CRF Specifications, Edit Check Specifications, User Acceptance Testing, open, clean and lock of databases)
  • Authors, reviews and/or approves various study related documents and plans (e.g., Data Management Plans, Data Transfer Agreements, CRF Completion Guidelines, Manual Review Guidelines)
  • Manages and performs ongoing data management activities including CRF review, query generation, receipt and reconciliation of external data, SAE reconciliation, data listing generation and production of CDM summary reports (e.g. metrics) within projected study timelines.
  • Performs medical coding of data using MedDRA & WHODrug dictionaries
  • Ensures clinical data management activities are executed in compliance with regulatory authority requirements and Good Clinical Practices (GCP)
  • Evaluates issues, recommend and implement solutions mitigation strategies as required
  • Assists or leads with vendor selection process for outsourced CDM activities
  • Oversees, as necessary, multiple External Service Provider (ESPs), contractors, or direct reports engaged to perform data management and EDC activities
  • Participates in governance of External Service Provider (ESPs) across studies
  • Participates in training of new hires and/or junior team members
  • Supports regulatory inspection activities
  • Oversees external data providers (e.g., IRT, central and specialty labs, patient diaries)
  • Presents at investigator’s meetings and other data management trainings for study
  • Escalates study related issues and communicates as appropriate with management and other functions
  • Represents Clinical Data Management at study team meetings and facilitates cross-functional activities (e.g. Clinical Data Listing Reviews, database lock activities)
  • Proactively addresses operational issues and clinical data questions
  • Provides updates on study timelines, vendor oversight and other study related activities
  • Liaises with the document specialists to ensure data management files are filed appropriately
  • Implements best practices and industry standards across all data management activities
  • Assists and leads department initiatives, process improvements, and cross functional initiatives
  • Performs other duties, as appropriate
  • Travel is variable and estimated at 10-20% domestic and international

 COMPETENCIES IDENTIFIED FOR SUCCESS

  • Excellent analytical and problem-solving skills
  • Outstanding organizational and time-management skills with ability to multitask and prioritize
  • Strong interpersonal and communication skills
  • Ability to effectively develop and manage relationships with internal and external stakeholders
  • Exceptional attention to detail
  • Flexible to changing priorities
  • Strong and positive work ethic

 EDUCATION, EXPERIENCE, AND OTHER REQUIREMENTS

  • Bachelor’s Degree (BA/BS) preferred
  • Minimum of five (5) years of direct Clinical Data Management experience, including at least 2 years of Study Lead Data Manager responsibilities.  
  • Experience with Electronic Data Capture (EDC) systems
  • Working knowledge of CDISC CDASH and CDISC SDTM standards/guidelines
  • Experience/training in the following areas: Good Clinical Practices (i.e. GxP Regulations; ICH Guidelines; Good Quality Practices), 21 CFR Part 11 and Computer Security (Part 11, Electronic Records; Electronic Signatures-Scope and Application; 21 CFR 11 and Industry Guidance; Computerized Systems Used in Clinical Trials), HIPAA, Drug Development and Approval Process, Data Management Overview
  • Proficiency in MS Office including Word, Excel, and PowerPoint required
  • SAS experience preferred but not required
  • Medical coding experience preferred but not required

Please visit our website, http://www.ionis.com, for more information about Ionis and to apply for this position; reference requisition #IONIS003496

Ionis offers an excellent benefits package! Follow this link for more details: Ionis Benefits

Full Benefits Link: https://www.ionis.com/careers/working-at-ionis/#:~:text=to%20Applicants%C2%A0%C2%BB-,Benefits,-Employees%20are%20rewarded

The pay scale for this position is $85,198 to $142,154

NO PHONE CALLS PLEASE. PRINCIPALS ONLY.

  Ionis Pharmaceuticals, Inc. and all its subsidiaries are proud to be EEO employers.

 

#LI-Remote

Required profile

Experience

Level of experience: Senior (5-10 years)
Industry :
Research
Spoken language(s):
Check out the description to know which languages are mandatory.

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