Clinical Data Manager – Contract

Adverum Biotechnologies

Clinical Data Manager overseeing clinical data management activities across studies at Adverum Biotechnologies, Inc. Focused on ensuring high-quality data and adherence to regulatory standards in a high-growth environment.

Posted 4/14/2026contractRemote • California • 🇺🇸 United StatesMid-LevelSenior💰 $70 - $85 per hourWebsite

Tech Stack

Tools & technologies

Google Cloud PlatformOracle

About the role

Key responsibilities & impact

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.

Requirements

What you’ll need

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.

Benefits

Comp & perks

🌐 Worldwide Post a Job Affiliates ❌ Jobs You've Hidden ⭐️ Saved Jobs ✅ Applied Jobs Account Adverum Biotechnologies Website LinkedIn All Job Openings 51 - 200 employees Founded 2013 🧬 Biotechnology 💊 Pharmaceuticals 💰 $217M Post-IPO Equity on 2020-08 Biotechnology
Pharmaceuticals Adverum Biotechnologies is a company focused on developing gene therapies to treat debilitating ocular diseases. Their mission is to establish gene therapy as a new standard of care, particularly in treating conditions like wet age-related macular degeneration (wet AMD), which is a leading cause of blindness globally. The company is advancing their investigational gene therapy Ixo-vec, designed to provide a long-lasting treatment through a single in-office administration, which could replace the current standard of frequent and painful eye injections. By leveraging their proprietary adeno-associated virus (AAV) vector platform, Adverum aims to transform the standard of care, improve accessibility to treatment, and achieve significant societal impact by restoring vision and preventing blindness. Clinical Data Manager – Contract Job not on LinkedIn 🔥 21 minutes ago 🏄 California – Remote 💵 $70 - $85 / hour ⏳ Contract/Temporary 🟡 Mid-level 🟠 Senior 📊 Data Scientist 🦅 H1B Visa Sponsor Apply Now Find Hiring Managers Customize resume for this job ☆ Save ☑️ Mark as applied ❌ Hide Report problem 📋 Description
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. 🎯 Requirements
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. Apply Now 📊 Check your resume score for this job Improve your chances of getting an interview by checking your resume score before you apply. Check Resume Score Similar Jobs Data Scientist 🕒 4 days ago NOVALINK SOLUTIONS LLC 51 - 200 📡 Telecommunications Website LinkedIn All Job Openings Data Scientist creating in-depth analyses to empower IDOH and other partners in Indiana. Mentoring junior staff and engaging with stakeholders to drive data solutions. 🇺🇸 United States – Remote ⏳ Contract/Temporary 🟢 Junior 🟡 Mid-level 📊 Data Scientist 🦅 H1B Visa Sponsor Senior Data Scientist 🕒 April 3 Apogee Global RMS 1 - 10 🔒 Cybersecurity 🤝 B2B 🎯 Recruiter Website LinkedIn All Job Openings Senior Data Scientist at Apogee Global RMS designing and deploying machine learning solutions. Collaborating with teams to support product innovation and strategic decision-making. 🇺🇸 United States – Remote ⏳ Contract/Temporary 🟠 Senior 📊 Data Scientist Senior Data Science Engineer 🕒 April 1 RapidSoft Corp 11 - 50 Website LinkedIn All Job Openings Senior Data Science Engineer developing data solutions in collaboration with software engineering teams at RapidSoft. Overseeing scalable data processing platforms for analytics and mentoring junior engineers. 🇺🇸 United States – Remote ⏳ Contract/Temporary 🟠 Senior 📊 Data Scientist Data Scientist 🕒 March 20 SpaceBound, Parent Company of SpaceBound Solutions 11 - 50 Website LinkedIn All Job Openings Data Scientist at Match Consulting leveraging advanced analytics to improve business performance. Implementing machine learning solutions and collaborating with stakeholders on data-driven insights. 🇺🇸 United States – Remote ⏳ Contract/Temporary 🟡 Mid-level 🟠 Senior 📊 Data Scientist Data Scientist – Short-term Contract 🕒 March 18 Capstone Integrated Solutions 51 - 200 Website LinkedIn All Job Openings Data Scientist supporting hands-on analysis, data preparation, and feature exploration at Capstone Integrated Solutions. Collaborating with senior data science leadership on predictive modeling. 🇺🇸 United States – Remote ⏳ Contract/Temporary 🟡 Mid-level 🟠 Senior 📊 Data Scientist View More Data Science Jobs 🌐 Worldwide Built by Lior Neu-ner. I'd love to hear your feedback — Get in touch via DM or support@remoterocketship.com Search Search Jobs by country Search jobs by city Search jobs by job title Search entry-level jobs Search junior-level jobs Search senior-level jobs Search jobs by tech stack Search jobs by contract type Search remote internships Search remote part-time jobs Remote jobs Anywhere in the World Companies Hiring Anywhere in the World Companies Hiring Sales People Anywhere in the World Companies Hiring Software Engineers Anywhere in the World Resources Advice Tips for finding remote jobs Interview questions and answers Resume examples Cover letter examples Post a job Affiliates Privacy policy Terms of service Job board SEO course AI Apply Copilot OpenClaw job finder Jobs by Country Remote jobs anywhere in the world (Worldwide remote jobs) Remote jobs United States Remote jobs Australia Remote jobs Brazil Remote jobs Canada Remote jobs France Remote jobs Ireland Remote jobs Germany Remote jobs Netherlands Remote jobs Spain Remote jobs UK Popular Jobs Remote data analyst jobs Remote customer support jobs Remote executive assistant jobs Remote marketing jobs Remote product designer jobs Remote product manager jobs Remote project manager jobs Remote recruiter jobs Remote sales jobs Remote software engineer jobs Jobs by Type Remote full-time jobs Remote part-time jobs Remote contract jobs Remote internship jobs Remote entry-level jobs Remote jobs with no experience required Remote junior jobs (1-3 years of experience) Digital nomad jobs Remote jobs with no degree required Freelance remote jobs Temporary remote jobs Remote jobs hiring now Stay at home mom jobs

ATS Keywords

✓ Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools

data managementEDC developmentCRF developmentUser Acceptance Testingdata reconciliationdata validationclinical trial processesdata management processesSAS datasetsregulatory submission

Soft Skills

organizational skillsattention to detaileffective communicationinterpersonal skillsproblem-solvinginitiativeflexibilityjudgmentability to prioritizeteamwork