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61 Merck Clinical Data Manager Jobs Hiring Near You

Trident Consulting

Clinical Data Manager

Aliso Viejo, CA · On-site

$48.65/hr

Clinical Data Manager Location: Aliso Viejo, CA - Onsite Type: W2 Contract Rate: $48.65/Hr on w2 The Clinical Data Manager II is responsible for study Data Management activities from study start up ...

Faeth Therapeutics

Clinical Data Manager

Austin, TX · Remote

$125K - $175K/yr

Faeth Therapeutics is seeking an experienced Clinical Data Manager to support clinical data management activities across two active clinical trials. This individual will play a critical role in ...

Katalyst

Clinical Data Manager

Austin, TX

The Clinical Data Manager (CDM) is responsible for the oversight, integrity, and quality of clinical trial data from collection through database lock * The CDM ensures that data is accurate ...

AccuScan Sciences

Clinical Data Manager

Milpitas, CA

Position Summary The Clinical Data Manager (CDM) is responsible for the end-to-end management, quality control, and analysis of clinical cohort data. This role ensures data integrity, identifies and ...

AccuScan Sciences

Clinical Data Manager

Milpitas, CA · On-site

Position Summary The Clinical Data Manager (CDM) is responsible for the end-to-end management, quality control, and analysis of clinical cohort data. This role ensures data integrity, identifies and ...

AccuScan Sciences

Clinical Data Manager

Milpitas, CA · On-site

Position Summary The Clinical Data Manager (CDM) is responsible for the end-to-end management, quality control, and analysis of clinical cohort data. This role ensures data integrity, identifies and ...

Katalyst

Clinical Data Manager

South Plainfield, NJ

Provide support and oversight for the CRO Data Management team. * Collaborate with the team on study design, protocol development, CRF design, statistical planning, and CSRs. * Review clinical study ...

Collabera

Clinical Data Manager

Irvine, CA

Clinical Data Manager Location: Irvine, CA USA 92618 Duration: 12 months (Strong Possibility of Extension) Employment Type: W2 Contingent Worker SUMMARY OF POSITION: As a key member of the Global ...

Katalyst

Clinical Data Manager

Boulder, CO

Develop and manage standard operation procedures (SOP and CLPs) for clinical investigation data management; Data Management Plans (DMP), eCRFs, user acceptance testing (UAT) plans and scripts; EDC ...

TScan Therapeutics

Clinical Data Manager

Waltham, MA · On-site

$130K - $150K/yr

Reporting to our Senior Clinical Data Manager the ideal candidate should have relevant experience in leading internal and external data management activities in oncology clinical studies and enjoy ...

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Clinical Data Manager

Clinical Data Manager

Trident Consulting

Aliso Viejo, CA • On-site

$48.65/hr

Other

Posted 15 days ago

Job description

Trident Consulting is seeking a "Clinical Data Manager” for one of our clients in "Aliso Viejo, CA - Onsite” a global leader in medical technology and pharmaceutical Industry.

Job Title: Clinical Data Manager

Location: Aliso Viejo, CA - Onsite

Type: W2 Contract

Rate: $48.65/Hr on w2

The Clinical Data Manager II is responsible for study Data Management activities from study start up to close out. Providing input into the data cleaning strategy and leading data cleaning efforts supporting Clinical Studies. This individual must possess strong project management and analytical skills and have the ability to review data using various reporting and analytics tools

Responsibilities:

  • Assist with writing, reviewing and management of key documents such as Data Management Plan, Project Plan, CRF completion guidelines, edit check specifications, data review guidelines.
  • Manage the User Acceptance Testing (UAT) of clinical databases including EDC.
  • Facilitate cross-functional Data Management meetings and discussions with Study Managers, Clinical Study Teams, Project Managers, Programming and Regulatory.
  • Oversee delivery of EDC study deliverables.
  • Oversee and support data cleaning efforts and perform regular data review across Glaukos studies. Perform data review to identify quality issues, data trends/outliers and generate queries as necessary.
  • Represent Data Management in study team meetings, providing data status metrics and providing guidance on issues related to data management
  • Perform review of study SAS and SDTM datasets.
  • Provide input and review of clinical data from external sources and assist in data reconciliation.
  • Work with programming to produce customized reports or data listings to facilitate data review and cleaning (e.g. safety reviews).
  • Generate reports or data listings for study teams as needed.
  • Assist medical coding, AE/SAE reconciliation.
  • Assist with CDM project documentation including vendor files in an audit- ready manner
  • Assist in the monitoring of enrollment information as collected in the database, provide status update to the study team.
  • Assist with the preparation of Data Management training materials used for Investigator meetings, in-house personnel and site staff.
  • Contribute to the development of departmental processes and procedures.

Requirements:

Work Experience:

  • 2-5 years of relevant industry experience
  • Experience working in Pharmaceutical/ Medical Device/ Biotechnology/ CRO industry in Clinical Data Management is required
  • Preferred experience in Ophthalmology Therapeutic area.
  • In-depth knowledge of FDA/ICH guidelines and industry/technology standard practices
  • In-depth knowledge of Data Management Practices and other regulatory guidelines specific to data management
  • Hands-on working knowledge of Electronic Data Capture (EDC) systems (e.g. Inform, RAVE, iMedNet, etc.), database design and database concepts required
  • Hands-on ability to review data and ability to use various data review tools
  • Project Management experience
  • Experience writing Data Management documentation (E.g. DMP, edit check specifications etc.)
  • Excellent verbal and written communication skills
  • Experience working with CDISC Standards (CDASH, SDTM)
  • Experience with SQL, SAS, Excel or other programming language a plus
  • BS or higher in biological science, nursing or other health-related discipline preferred

About Trident Consulting

Trident Consulting is an award-winning staffing and consulting firm headquartered in San Ramon, CA. Since 2005, we've partnered with Fortune 500 and high-growth companies to deliver high-quality talent across technology, engineering, business operations, and professional services.

We specialize in contract, contract-to-hire, and direct hire placements, supporting roles across IT, data & analytics, cloud, cybersecurity, finance & accounting, HR, operations, and more. With a strong focus on hard-to-fill and niche positions, our global recruiting engine enables us to deliver speed, quality, and scale.

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About Trident Consulting

Sourced by ZipRecruiter

Trident Consulting is a certified 100% woman- and minority-owned staffing company, incorporated in 2005. Some of our achievements include making it to the Inc. 5000 list and Bay Area's list of Top 100 fastest growing companies.

Industry

It services

Company size

51 - 200 Employees

Headquarters location

Dublin, CA, US

Year founded

2005

Social media

Twitter

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