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Contract Clinical Data Manager Jobs (NOW HIRING)

Belcan

Clinical Data Manager

Durham, NC · On-site

$55 - $65/hr

Clinical Data Manager Location ... Durham, NC Duration: 09 Months contract(Potential temp to Perm) Payrate: $55/hr. - $65/hr ...

Belcan

Clinical Data manager

Durham, NC · On-site

$55 - $65/hr

Right Away Contract: 9 months Keywords: #DurhamJobs; #ClinicalDatamanagerJobs; Job Summary: The Clinical Data Manager will apply his or her knowledge of Clinical Research, therapeutic areas and ...

TalentBurst, Inc.

Clinical Data manager

Durham, NC

Title: Clinical Data manager Location: Durham, NC 27709 Duration: 9 Months Job Summary: The ... We specialize in Contract and Contract to Permanent roles across many industries and have direct ...

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Pharmaron

Clinical Data Manager

Somerset, NJ · On-site

$60K - $75K/yr

Clinical Data Manager FLSA Status: Exempt Location ... Onsite (Somerset, New Jersey) Salary: $60,000 - $75,000 Pharmaron is a global CRO (Contract ...

Pharmaron

Clinical Data Manager

Somerset, NJ · On-site

$60K - $75K/yr

Clinical Data Manager FLSA Status: Exempt Location ... Onsite (Somerset, New Jersey) Salary: $60,000 - $75,000 Pharmaron is a global CRO (Contract ...

Sumitomopharma

OR

$130.40K - $163K/yr

Execute and manage all in house clinical data management activities for assigned oncology trials in accordance with ICH/GCP, regulatory requirements, and internal SOPs. * Support and contribute to ...

CYNET SYSTEMS

Clinical Data Manager

Sunnyvale, CA · On-site

$70 - $75/hr

Support clinical data review requirements from Lead data manager. * Create customise data review listings for study per specifications from lead data manager. * Provide clinical data management ...

Sumitomo Pharma

Clinical Data Manager

$130.40K - $163K/yr

Execute and manage all in house clinical data management activities for assigned oncology trials in accordance with ICH/GCP, regulatory requirements, and internal SOPs. * Support and contribute to ...

Faeth Therapeutics

Clinical Data Manager

San Francisco, CA · 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 ...

Faeth Therapeutics

Clinical Data Manager

San Francisco, CA · On-site

$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 ...

MapLight Therapeutics

Clinical Data Manager

Burlington, MA · On-site

$145K - $160K/yr

We are seeking a highly skilled and motivated Clinical Data Manager to join our Clinical Data Management team. Reporting to the Associate Director, the Clinical Data Manager, will play a pivotal role ...

ImmunityBio, Inc.

Clinical Data Manager

Position Summary The Clinical Data Manager is an expert in clinical data management with demonstrated capability in building and maintaining clinical trial databases. They contribute to process ...

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How much do contract clinical data manager jobs pay per hour?

As of May 28, 2026, the average hourly pay for contract clinical data manager in the United States is $57.17, according to ZipRecruiter salary data. Most workers in this role earn between $45.19 and $68.03 per hour, depending on experience, location, and employer.

What is a Contract Clinical Data Manager job?

A Contract Clinical Data Manager is a temporary or freelance professional responsible for overseeing and managing clinical trial data for pharmaceutical, biotech, or CRO companies. They ensure data integrity, compliance with regulatory standards, and support database design, data cleaning, and reporting. Contract roles offer flexibility and typically involve working on specific projects or trials for a set duration.

What are the key skills and qualifications needed to thrive in the Contract Clinical Data Manager position, and why are they important?

To thrive as a Contract Clinical Data Manager, you need strong expertise in clinical data management, a background in life sciences, and familiarity with regulatory guidelines such as FDA or ICH-GCP. Proficiency in database systems like Medidata Rave or Oracle Clinical, coupled with knowledge of CDISC standards and, in many cases, a CCDM certification, is highly valued. Excellent attention to detail, strong organizational skills, and effective communication help distinguish top performers in this role. These abilities are crucial for ensuring compliant, high-quality data that supports successful clinical trials on a contractual or project basis.

What does a typical day look like for a Contract Clinical Data Manager?

A Contract Clinical Data Manager typically spends their days overseeing data collection, validation, and entry processes, ensuring that clinical trial data meets quality and regulatory standards. This role often involves close collaboration with data entry teams, biostatisticians, and clinical project managers to resolve discrepancies and maintain data integrity. Daily responsibilities may include designing case report forms, conducting data reviews, managing database queries, and preparing data for interim or final analyses. Working on a contract basis, you may manage multiple projects concurrently and must be adaptable to varying timelines and sponsor requirements.
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Contract Clinical Data Manager jobs near you
Clinical Data Manager (Contract)

Clinical Data Manager (Contract)

Adverum Biotechnologies, Inc.

Redwood City, CA

Contractor

Posted 14 days ago

Job description

Adverum Biotechnologies, Inc., a wholly owned subsidiary of Eli Lilly and Company is a mission-driven clinical-stage company that aims to establish gene therapy as a new standard of care for highly prevalent ocular diseases with the aspiration of developing functional cures to restore vision and prevent blindness. Leveraging the research capabilities of its proprietary intravitreal (IVT) platform, Adverum is developing durable, single-administration therapies designed to be delivered in physicians' offices to eliminate the need for frequent ocular injections to treat these diseases. By overcoming the challenges associated with current treatment paradigms for these debilitating ocular diseases, Adverum aspires to transform the standard of care, preserve vision, and create a profound societal impact around the globe.
 
The Clinical Data Manager (CDM) is responsible for data management activities across one or more studies from study start-up through study closure to ensure completion per established project team goals and objectives, including oversight of the CRO DM Vendor, if the project is outsourced. The CDM / Senior CDM will report to the Head of Clinical Data Management and will work closely with a cross-functional team in a fast-paced high growth environment team to ensure that clinical data are complete, high quality and delivered on time and budget.
 
This is a 6-12 month contract.  
 
Note to Recruiters and Agencies
All recruiter and agency inquiries must go through Adverum's internal Talent Acquisition team.  Unsolicited resumes sent to Adverum will be considered property of Adverum.   Agencies must be expressly engaged by Adverum's Talent Acquisition team for any requisition.  Direct contact with hiring managers by agencies will not be tolerated and may affect your ability to work with Adverum in the future.
What you'll do:
  • Responsible for compliance with regulatory and ICH guidelines, GCPs, company guidelines and Standard Operating Procedures, and CDM best practices.
  • Independently serves as the lead point of contact for all data management study-related communications.
  • Independently leads EDC development, including CRF development, EDC specification process, edit check development and User Acceptance Testing including test scripts and execution logs, issue logs, and UAT summary reports.
  • Reviews and assists in the development of study documents drafted by CROs such as Data Management Plans, Data Validation Specifications, eCRF Completion Guidelines, Data Review Plans, Data Transfer Agreements, and other cross-functional study documents that may require data management input.
  • Ensures the quality of clinical data within the EDC and other databases through regular data review and external data reconciliation processes and communicates any outstanding issues to the cross-functional teams.
  • Monitors and tracks the quality of all data management deliverables.
  • Leads data deliverables including snapshots for DMC, investor relations, publications, etc., and interim and final database locks, in collaboration with the CRO DM Vendor.
  • Effectively oversees contracted vendors, or vendor groups within CRO, to ensure data are complete, accurate and delivered within agreed on timelines.
  • Leads and facilitates Data Review Meetings with the cross-functional team, presenting metrics, trends, risks, and or issues.
  • Actively participates in team meetings - DM or cross-functional.
  • Coordinates transfers of SAS datasets or external data transfers from CROs.
  • Support TFL reviews, yearly regulatory submission requirements, compilation of CSRs, etc.
  • Responsible for TMF maintenance of data management-related study documents.
  • Responsible for archiving trial(s) and associated documentation upon trial(s) completion.
About You:
  • Bachelor's degree or equivalent in life science, computer science, or related discipline.
  • 5+ years (CDM) / 8+ years (Sr. CDM) of experience working within a pharmaceutical or CRO environment, with experience in managing Phase I, II and/or III studies, from start-up through closure.
  • Demonstrated proficiency in various EDC Systems within the last 3 years.
  • Demonstrated proficiency in data management processes, clinical trial processes, and applicable regulatory requirements.
  • Good working knowledge of ICH, FDA, and GCP regulations and guidelines.
  • Experience with web-based Electronic Data Capture (EDC such as iMedidata Rave, Oracle InForm, etc.), clinical data management systems - eCOA, IRT, and industry wide thesauri, such as MedDRA and WHO Drug.
  • Experience in managing CRO Data Management vendors.
  • Knowledge of industry standards (CDISC, CDASH, SDTM, etc.).
  • Demonstrated proficiency in Microsoft Word, Project, PowerPoint, Office, and Excel.
  • Excellent organizational skills and attention to detail.
  • Effective communication (verbal/written) and interpersonal skills.
  • Able to set priorities and juggle multiple projects and demands.
  • Able to think critically and independently and be a proactive problem-solver.
  • Able to lead and work independently while exercising initiative, flexibility, and sound judgment.
  • Comfortable working in a fast-paced environment with different levels of the company including senior level management.
  • Proven ability to work both independently and in a team setting.
$70 - $85 an hour
This is a 6-12 month contract position.  The hourly rate is from $70-85 per hour, depending on the experience level.  
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