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 ...

62 Biogen Clinical Data Manager Jobs Hiring Near You
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 ...
Clinical Data Manager
Maple Grove, MN · On-site
Clinical Data Manager Job Location: Maple Grove, MN 55311 Contract: 6+ Months (High possibility of conversion) Shift: 8 AM - 4 PM CST 100% Onsite Role Job Role: The Clinical Data Manager is ...
New
Clinical Data Manager
Maple Grove, MN · On-site
Clinical Data Manager Job Location: Maple Grove, MN 55311 Contract: 6+ Months (High possibility of conversion) Shift: 8 AM - 4 PM CST 100% Onsite Role Job Role: The Clinical Data Manager is ...
New
Clinical Data Manager
Maple Grove, MN · On-site
Clinical Data Manager Job Location: Maple Grove, MN 55311 Contract: 6+ Months (High possibility of conversion) Shift: 8 AM - 4 PM CST 100% Onsite Role Job Role: The Clinical Data Manager is ...
New
Clinical Data Manager
Maple Grove, MN · On-site
Clinical Data Manager Job Location: Maple Grove, MN 55311 Contract: 6+ Months (High possibility of conversion) Shift: 8 AM - 4 PM CST 100% Onsite Role Job Role: The Clinical Data Manager is ...
New
Clinical Data Manager
Maple Grove, MN · On-site
Clinical Data Manager Job Location: Maple Grove, MN 55311 Contract: 6+ Months (High possibility of conversion) Shift: 8 AM - 4 PM CST 100% Onsite Role Job Role: The Clinical Data Manager is ...
New
Clinical Data Manager
Maple Grove, MN · On-site
Clinical Data Manager Job Location: Maple Grove, MN 55311 Contract: 6+ Months (High possibility of conversion) Shift: 8 AM - 4 PM CST 100% Onsite Role Job Role: The Clinical Data Manager is ...
New
Clinical Data Manager
Cambridge, MA · On-site
Managing the collection, validation, coding and storage of clinical program data; enforcing standardization to maximize global data integration and inter-program efficiency. Directing the work of ...
Clinical Data Manager
Cambridge, MA · On-site
Managing the collection, validation, coding and storage of clinical program data; enforcing standardization to maximize global data integration and inter-program efficiency. Directing the work of ...
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 ...
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 ...
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 ...
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 ...
Clinical Data Manager
Maple Grove, MN · On-site
Clinical Data Manager Job Location: Maple Grove, MN 55311 Contract: 6+ Months (High possibility of conversion) Shift: 8 AM - 4 PM CST 100% Onsite Role Job Role: The Clinical Data Manager is ...
New
Clinical Data Manager
Maple Grove, MN · On-site
Clinical Data Manager Job Location: Maple Grove, MN 55311 Contract: 6+ Months (High possibility of conversion) Shift: 8 AM - 4 PM CST 100% Onsite Role Job Role: The Clinical Data Manager is ...
New
Clinical Data Manager
Saint Paul, MN · On-site
Merit Medical Systems, Inc. seeks an experienced Data Manager to ensure data integrity across clinical studies. You will define databases, manage validations, and support eCRF specifications while ...
Clinical Data Manager
Saint Paul, MN · On-site
Merit Medical Systems, Inc. seeks an experienced Data Manager to ensure data integrity across clinical studies. You will define databases, manage validations, and support eCRF specifications while ...
Clinical Data Management System experience (e.g., Clintrial, Oracle Clinical) and understanding of database/programming concepts preferred. * High level of knowledge in the use of Data Management ...
Clinical Data Management System experience (e.g., Clintrial, Oracle Clinical) and understanding of database/programming concepts preferred. * High level of knowledge in the use of Data Management ...
Clinical Data Manager
Saint Paul, MN · On-site
Merit Medical Systems, Inc. seeks an experienced Data Manager to ensure data integrity across clinical studies. You will define databases, manage validations, and support eCRF specifications while ...
Clinical Data Manager
Saint Paul, MN · On-site
Merit Medical Systems, Inc. seeks an experienced Data Manager to ensure data integrity across clinical studies. You will define databases, manage validations, and support eCRF specifications while ...
Women's Health Account Manager (Neuropsychiatry) - Manhattan and Bronx, NY
New York, NY · On-site
$138K - $185K/yr
Biogen is seeking a collaborative, strategic, and results-oriented Women's Health Account Manager ... Communicate complex clinical data, screening protocols, treatment pathways, market access policies ...
Women's Health Account Manager (Neuropsychiatry) - Manhattan and Bronx, NY
New York, NY · On-site
$138K - $185K/yr
Biogen is seeking a collaborative, strategic, and results-oriented Women's Health Account Manager ... Communicate complex clinical data, screening protocols, treatment pathways, market access policies ...
Clinical Data Manager
Maple Grove, MN · On-site
$45 - $47/hr
Clinical Data Manager Location: Maple Grove, MN Duration: 7 Months 100% Onsite Summary: The Clinical Data Manager is responsible for managing the development, documentation, and execution of risk ...
Clinical Data Manager
Maple Grove, MN · On-site
$45 - $47/hr
Clinical Data Manager Location: Maple Grove, MN Duration: 7 Months 100% Onsite Summary: The Clinical Data Manager is responsible for managing the development, documentation, and execution of risk ...
Clinical Data Manager
Irvine, CA · On-site
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 ...
Clinical Data Manager
Irvine, CA · On-site
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 ...
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 ...
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 ...
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 ...
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 ...
Senior Clinical Data Manager,Oncology Project Data Management level. Perform DM activities for in-house and outsourced trials: protocolreview, CRF development, database set up activities, data ...
Senior Clinical Data Manager,Oncology Project Data Management level. Perform DM activities for in-house and outsourced trials: protocolreview, CRF development, database set up activities, data ...
Senior Clinical Data Manager, Oncology -Project Data Management level. -Perform DM activities for in-house and outsourced trials: protocol review, CRF development, database set up activities, data ...
Senior Clinical Data Manager, Oncology -Project Data Management level. -Perform DM activities for in-house and outsourced trials: protocol review, CRF development, database set up activities, data ...
Lead and manage clinical data management activities for oncology clinical trials, ensuring adherence to project timelines, budgets, and quality standards. * Provide strategic oversight and direction ...
Lead and manage clinical data management activities for oncology clinical trials, ensuring adherence to project timelines, budgets, and quality standards. * Provide strategic oversight and direction ...
Lead and manage clinical data management activities for oncology clinical trials, ensuring adherence to project timelines, budgets, and quality standards. * Provide strategic oversight and direction ...
Lead and manage clinical data management activities for oncology clinical trials, ensuring adherence to project timelines, budgets, and quality standards. * Provide strategic oversight and direction ...
Biogen Jobs Information
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87% of people say they get paid breaks.
Based on data from 15 people who took the Breakroom Quiz between January 2025 and June 2026.
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85% of people say they would get paid if they were sick but scheduled to work.
Based on data from 20 people who took the Breakroom Quiz between December 2024 and June 2026.
At Biogen, are sick days and vacation days separate paid time off?
90% of people say they don’t have to use vacation days when they’re out sick.
Based on data from 10 people who took the Breakroom Quiz between August 2025 and June 2026.
Is the health insurance from Biogen affordable enough for their workers?
100% of people say the health insurance costs are okay
Based on data from 10 people who took the Breakroom Quiz between March 2025 and June 2026.
Do people get paid time off at Biogen?
91% of people say they get paid time off.
Based on data from 11 people who took the Breakroom Quiz between July 2025 and June 2026.
Do workers at Biogen worry about hours?
92% of people report they don’t worry about getting enough hours.
Based on data from 13 people who took the Breakroom Quiz between January 2025 and June 2026.
Do Biogen workers get to choose the shifts they work?
82% report that they have enough control over which shifts they work.
Based on data from 11 people who took the Breakroom Quiz between January 2025 and April 2026.
How easy is it for Biogen workers to change shifts?
80% of people report that it’s easy to change shifts if they need to.
Based on data from 5 people who took the Breakroom Quiz between January 2025 and June 2026.
How easy is it to get time off at Biogen?
100% of people report it’s easy to get time off.
Based on data from 19 people who took the Breakroom Quiz between December 2024 and June 2026.
Do Biogen managers change schedules at the last minute?
85% of people say their manager doesn’t change their shift schedule at the last minute.
Based on data from 13 people who took the Breakroom Quiz between January 2025 and June 2026.
Do jobs at Biogen spill into time workers aren’t paid for?
15% of people report that their job takes up time that they don’t get paid for.
Based on data from 13 people who took the Breakroom Quiz between January 2025 and June 2026.
How easy is it to take sick days at Biogen?
95% of people report that it’s easy to take time off if they are sick.
Based on data from 19 people who took the Breakroom Quiz between December 2024 and June 2026.
Is working at Biogen good if you’re a parent or caregiver?
100% of people who care for a child or other relative report this is a good place to work.
Based on data from 5 people who took the Breakroom Quiz between March 2025 and June 2026.
Do people at Biogen feel treated with respect by their managers?
94% of people say they’re treated with respect by their managers.
Based on data from 18 people who took the Breakroom Quiz between December 2024 and June 2026.
Do people at Biogen get to take their breaks without interruption?
89% of people report that they get to take their breaks without interruption.
Based on data from 18 people who took the Breakroom Quiz between January 2025 and June 2026.
Is it stressful to work at Biogen?
38% of people say they often feel stressed out at work.
Based on data from 16 people who took the Breakroom Quiz between December 2024 and June 2026.
Do people at Biogen enjoy their jobs?
100% of people report they enjoy their job.
Based on data from 17 people who took the Breakroom Quiz between December 2024 and June 2026.
Do people at Biogen recommend working with their team?
85% of people report that they would recommend working with their immediate team to a friend.
Based on data from 20 people who took the Breakroom Quiz between December 2024 and June 2026.
Do people get enough training when they start at Biogen?
82% of people report they got enough training when they started working here.
Based on data from 17 people who took the Breakroom Quiz between December 2024 and June 2026.
Do people get support to advance at Biogen?
In the last year, 88% of people report being given support to advance their career here.
Based on data from 17 people who took the Breakroom Quiz between December 2024 and June 2026.
Do people think Biogen’s headquarters understands what’s happening where they work?
67% of people think that this employer’s headquarters or owners don’t have a good understanding of what’s really happening where they work.
Based on data from 15 people who took the Breakroom Quiz between December 2024 and June 2026.
Do workers feel well informed about how Biogen is doing?
76% of people feel that they are kept well informed about how the company is doing as a whole.
Based on data from 17 people who took the Breakroom Quiz between December 2024 and June 2026.
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Job description
- 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, consistent, and meets regulatory and protocol-specific requirements
- This role collaborates closely with cross-functional teams, including Clinical Operations, Biostatistics, Medical Writing, and Regulatory Affairs, to support timely and compliant study execution
- Design and review Case Report Forms (CRFs) and Electronic Data Capture (EDC) systems to ensure accurate and complete data capture aligned with the study protocol
- Develop and maintain data management plans (DMPs), data validation specifications, and CRF completion guidelines
- Oversee data cleaning activities, including the generation, review, and resolution of data queries in collaboration with clinical sites and study teams
- Perform ongoing data reviews to identify trends, inconsistencies, or protocol deviations
- Ensure adherence to data standards (e.g., CDISC, SDTM) and regulatory requirements (e.g., FDA, ICH-GCP)
- Manage database lock activities and contribute to the preparation of clinical study reports (CSRs)
- Serve as the primary point of contact for data management vendors and oversee their deliverables
- Participate in study team meetings and provide status updates related to data quality and timelines
- Support audit readiness and participate in regulatory inspections when required
- Bachelor's degree in Life Sciences, Computer Science, Health Informatics, or related field
- Minimum of 3-5 years of experience in clinical data management within a pharmaceutical, biotech, or CRO environment
- Proficiency in EDC platforms (e.g., Medidata Rave, Oracle InForm, Veeva, REDCap)
- Strong understanding of ICH-GCP, FDA regulations, and CDISC standards
- Experience with data listings, query management, edit check programming, and coding dictionaries (e.g., MedDRA, WHODrug)
- Excellent organizational, analytical, and problem-solving skills
- Strong communication and collaboration skills across cross-functional teams
About Katalyst Healthcares & Life Sciences
Sourced by ZipRecruiter
Katalyst HealthCares & Life Sciences is a Global Contract Research Organization that provides services in Clinical Research, Manufacturing & Quaity, Regulatory Affairs Areas.. Industries Serving: Pharmaceutical Bio-Pharmaceutical Medical Device Cosmeceuticals & Cosmetics Food & Beverage Clinical Research Scientific Areas Covering: Clinical Research Manufacturing Quality & Validations Regulatory Affairs Intellectual Property Through our in-house team expertise, associates and alliances in the US, Europe and Asia, we can rapidly deliver services, technology, processes and workforce globally, either virtually or integrate into client project space, providing oversight and expertise for individual needs to total end-to-end support for all kinds of clinical trials of Pharma, Biotech, Medical Device and all other scientific products and their manufacturing.
Industry
Scientific research and development services
Company size
51 - 200 Employees
Headquarters location
South Plainfield, NJ, US