Clinical Data Manager
Austin, TX · On-site
Clinical Data Manager 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 ...
62 Merck Clinical Data Manager Jobs Hiring Near You
Clinical Data Manager
Austin, TX · On-site
Clinical Data Manager 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 ...
The Clinical Data Manager performs activities pertaining to the conduct of Phase I-III clinical trials in accordance with ICH/Good Clinical Practices (GCP) and other relevant procedures and ...
The Clinical Data Manager performs activities pertaining to the conduct of Phase I-III clinical trials in accordance with ICH/Good Clinical Practices (GCP) and other relevant procedures and ...
Clinical Data Manager
Charleston, WV · On-site +1
Clinical Data Manager The Clinical Data Manager performs activities pertaining to the conduct of Phase I-III clinical trials in accordance with ICH/Good Clinical Practices (GCP) and other relevant ...
Clinical Data Manager
Charleston, WV · On-site +1
Clinical Data Manager The Clinical Data Manager performs activities pertaining to the conduct of Phase I-III clinical trials in accordance with ICH/Good Clinical Practices (GCP) and other relevant ...
Clinical Data Manager
$100K - $130K/yr
The Data Manager effectively works with a variety of key stakeholders including clinicians, allied healthcare personnel, clients, vendors, and iuvo Clinical staff. ESSENTIAL DUTIES AND ...
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Clinical Data Manager
$100K - $130K/yr
The Data Manager effectively works with a variety of key stakeholders including clinicians, allied healthcare personnel, clients, vendors, and iuvo Clinical staff. ESSENTIAL DUTIES AND ...
Qualifications Lead clinical data manager with 3 -5 years of Sponsor or CRO or Academic experience Understanding of clinical data management processes Project management experience of clinical trials ...
Qualifications Lead clinical data manager with 3 -5 years of Sponsor or CRO or Academic experience Understanding of clinical data management processes Project management experience of clinical trials ...
Clinical Data Manager
King Of Prussia, PA · On-site
Duties: * Develop, configure, and verify clinical databases and electronic data capture (EDC) systems, including case report forms (CRFs). * Design and Implement detailed data management plans ...
Clinical Data Manager
King Of Prussia, PA · On-site
Duties: * Develop, configure, and verify clinical databases and electronic data capture (EDC) systems, including case report forms (CRFs). * Design and Implement detailed data management plans ...
Clinical Data Manager
East Hanover, NJ · On-site
Provide timely and professional ongoing management of Data Management deliverables and of clinical trial data with respect to cost, quality and timelines for assigned trials managed within Clinical ...
Clinical Data Manager
East Hanover, NJ · On-site
Provide timely and professional ongoing management of Data Management deliverables and of clinical trial data with respect to cost, quality and timelines for assigned trials managed within Clinical ...
Clinical Data Manager
Santa Clara, CA · On-site
Clinical Data Manager Location: Santa Clara, CA Duration: 24 Months Job ID: ABLJP00048431 Participates in or leads the review of Clinical Research (CR) documents (e.g., protocols, reports and ...
Clinical Data Manager
Santa Clara, CA · On-site
Clinical Data Manager Location: Santa Clara, CA Duration: 24 Months Job ID: ABLJP00048431 Participates in or leads the review of Clinical Research (CR) documents (e.g., protocols, reports and ...
Clinical Data Manager
Raleigh, NC · On-site
Clinical Data Manager The Clinical Data Manager performs activities pertaining to the conduct of Phase I-III clinical trials in accordance with ICH/Good Clinical Practices (GCP) and other relevant ...
Clinical Data Manager
Raleigh, NC · On-site
Clinical Data Manager The Clinical Data Manager performs activities pertaining to the conduct of Phase I-III clinical trials in accordance with ICH/Good Clinical Practices (GCP) and other relevant ...
Clinical Data Manager
Somerset, NJ · On-site
Job Summary The Clinical Data Manager is responsible for supporting all data management activities for research studies in compliance with departmental SOPs and all regulatory guidelines. The ...
Clinical Data Manager
Somerset, NJ · On-site
Job Summary The Clinical Data Manager is responsible for supporting all data management activities for research studies in compliance with departmental SOPs and all regulatory guidelines. The ...
Clinical Data Manager
Austin, TX · On-site
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
Austin, TX · On-site
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 ...
Job Summary The Clinical Data Manager is responsible for supporting all data management activities for research studies in compliance with departmental SOPs and all regulatory guidelines. The ...
Job Summary The Clinical Data Manager is responsible for supporting all data management activities for research studies in compliance with departmental SOPs and all regulatory guidelines. The ...
Clinical Data Manager Location: Irvine, CA Duration: 12 Months Job Functions and Duties Performed: 1. Lead internal and outsourced Clinical Data Management activities in support of Clinical Research ...
Clinical Data Manager Location: Irvine, CA Duration: 12 Months Job Functions and Duties Performed: 1. Lead internal and outsourced Clinical Data Management activities in support of Clinical Research ...
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 ...
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 ...
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 ...
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
Somerset, NJ · On-site
Job Summary The Clinical Data Manager is responsible for supporting all data management activities for research studies in compliance with departmental SOPs and all regulatory guidelines. The ...
Clinical Data Manager
Somerset, NJ · On-site
Job Summary The Clinical Data Manager is responsible for supporting all data management activities for research studies in compliance with departmental SOPs and all regulatory guidelines. The ...
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 ...
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 ...
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 ...
Merck Jobs Information
Do workers at Merck get paid breaks?
Sometimes. Only some people get paid breaks.
44% of people say they don’t get paid breaks.
Based on data from 25 people who took the Breakroom Quiz between December 2024 and September 2026.
44% of people say they don’t get paid breaks.
Based on data from 25 people who took the Breakroom Quiz between December 2024 and September 2026.
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Yes. Most people get paid when they’re sick.
83% of people say they would get paid if they were sick but scheduled to work.
Based on data from 47 people who took the Breakroom Quiz between December 2024 and September 2026.
83% of people say they would get paid if they were sick but scheduled to work.
Based on data from 47 people who took the Breakroom Quiz between December 2024 and September 2026.
At Merck, are sick days and vacation days separate paid time off?
Sick days and vacation days are separate paid time off.
81% of people say they don’t have to use vacation days when they’re out sick.
Based on data from 26 people who took the Breakroom Quiz between May 2025 and September 2026.
81% of people say they don’t have to use vacation days when they’re out sick.
Based on data from 26 people who took the Breakroom Quiz between May 2025 and September 2026.
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Most people say the health insurance costs are okay.
100% of people say the health insurance costs are okay
Based on data from 34 people who took the Breakroom Quiz between March 2025 and September 2026.
100% of people say the health insurance costs are okay
Based on data from 34 people who took the Breakroom Quiz between March 2025 and September 2026.
Do people get paid time off at Merck?
Most people get paid time off work.
93% of people say they get paid time off.
Based on data from 29 people who took the Breakroom Quiz between May 2025 and September 2026.
93% of people say they get paid time off.
Based on data from 29 people who took the Breakroom Quiz between May 2025 and September 2026.
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Most people find out their schedule less than four weeks ahead of time.
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Most people don’t worry about getting enough hours.
93% of people report they don’t worry about getting enough hours.
Based on data from 27 people who took the Breakroom Quiz between December 2024 and September 2026.
93% of people report they don’t worry about getting enough hours.
Based on data from 27 people who took the Breakroom Quiz between December 2024 and September 2026.
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Some people don’t get to choose which shifts they work.
50% report that they don’t have enough control over which shifts they work.
Based on data from 24 people who took the Breakroom Quiz between December 2024 and September 2026.
50% report that they don’t have enough control over which shifts they work.
Based on data from 24 people who took the Breakroom Quiz between December 2024 and September 2026.
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Most people find it hard to change shifts.
75% of people report that it’s hard to change shifts if they need to.
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75% of people report that it’s hard to change shifts if they need to.
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Most people find it easy to get time off.
87% of people report it’s easy to get time off.
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87% of people report it’s easy to get time off.
Based on data from 45 people who took the Breakroom Quiz between December 2024 and September 2026.
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Most managers don’t change people’s schedules at the last minute.
93% of people say their manager doesn’t change their shift schedule at the last minute.
Based on data from 29 people who took the Breakroom Quiz between December 2024 and September 2026.
93% of people say their manager doesn’t change their shift schedule at the last minute.
Based on data from 29 people who took the Breakroom Quiz between December 2024 and September 2026.
Do jobs at Merck spill into time workers aren’t paid for?
Rarely. The job doesn't usually spill into unpaid time.
16% of people report that their job takes up time that they don’t get paid for.
Based on data from 31 people who took the Breakroom Quiz between December 2024 and September 2026.
16% of people report that their job takes up time that they don’t get paid for.
Based on data from 31 people who took the Breakroom Quiz between December 2024 and September 2026.
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Most people find it easy to take sick days.
85% of people report that it’s easy to take time off if they are sick.
Based on data from 48 people who took the Breakroom Quiz between December 2024 and September 2026.
85% of people report that it’s easy to take time off if they are sick.
Based on data from 48 people who took the Breakroom Quiz between December 2024 and September 2026.
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Most parents and caregivers say this is a good place to work.
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83% of people who care for a child or other relative report this is a good place to work.
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79% of people say they’re treated with respect by their managers.
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Most people get breaks without interruption.
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Based on data from 40 people who took the Breakroom Quiz between December 2024 and September 2026.
80% of people report that they get to take their breaks without interruption.
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Most people feel stressed here.
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Based on data from 52 people who took the Breakroom Quiz between December 2024 and September 2026.
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Based on data from 38 people who took the Breakroom Quiz between December 2024 and September 2026.
74% of people report they enjoy their job.
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44% of people report that they wouldn’t recommend working with their immediate team to a friend.
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Most people got enough training when they started.
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77% of people report they got enough training when they started working here.
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Most people are given support to advance their career here.
In the last year, 68% of people report being given support to advance their career here.
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In the last year, 68% of people report being given support to advance their career here.
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Most people think headquarters doesn’t understand what’s happening where they work.
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83% 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 46 people who took the Breakroom Quiz between December 2024 and September 2026.
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Only some people feel well informed about how the company is doing.
38% of people feel that they aren’t kept well informed about how the company is doing as a whole.
Based on data from 45 people who took the Breakroom Quiz between December 2024 and September 2026.
38% of people feel that they aren’t kept well informed about how the company is doing as a whole.
Based on data from 45 people who took the Breakroom Quiz between December 2024 and September 2026.
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Clinical Data Manager
Austin, TX • On-site
Katalyst HealthCares & Life Sciences
• Scientific Research and Development Services • 51 - 200 employees51 - 200 employees
Full-time
This job post has expired today. Applications are no longer accepted.
Job description
Clinical Data Manager
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
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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