Senior Clinical Data Manager
Durham, NC · On-site
What the Senior Clinical Data Manager does at Worldwide Oversee, lead, manage, and provide technicalexpertisewithin the assigned projects to ensure that they are executed in an efficient,accurate ...

Durham, NC · On-site
What the Senior Clinical Data Manager does at Worldwide Oversee, lead, manage, and provide technicalexpertisewithin the assigned projects to ensure that they are executed in an efficient,accurate ...
Durham, NC · On-site
What the Senior Clinical Data Manager does at Worldwide Oversee, lead, manage, and provide technicalexpertisewithin the assigned projects to ensure that they are executed in an efficient,accurate ...
Culver City, CA · On-site +1
Position Summary The Senior Clinical Data Manager is an expert in clinical data management with demonstrated capability in building and maintaining clinical trial databases. They contribute to ...
Culver City, CA · On-site +1
Position Summary The Senior Clinical Data Manager is an expert in clinical data management with demonstrated capability in building and maintaining clinical trial databases. They contribute to ...
Durham, NC · On-site +1
What the Senior Clinical Data Manager does at Worldwide Oversee, lead, manage, and provide technical expertise within the assigned projects to ensure that they are executed in an efficient, accurate ...
Durham, NC · On-site +1
What the Senior Clinical Data Manager does at Worldwide Oversee, lead, manage, and provide technical expertise within the assigned projects to ensure that they are executed in an efficient, accurate ...
Kennesaw, GA · On-site
The Sr. Clinical Data Manager is responsible for data management operations and for the organization, coordination and execution of data management activities for assigned studies and projects. This ...
Kennesaw, GA · On-site
The Sr. Clinical Data Manager is responsible for data management operations and for the organization, coordination and execution of data management activities for assigned studies and projects. This ...
... Clinical Data Manager manages the general conduct of project assigned tasks as the Lead Data Manager or under advisement from senior members of the Data Management Team. Responsible for oversight and ...
... Clinical Data Manager manages the general conduct of project assigned tasks as the Lead Data Manager or under advisement from senior members of the Data Management Team. Responsible for oversight and ...
Strongknowledge of data management best practices & technologies as applied to clinical trials. * Excellent communication and interpersonal skills to collaborate with cross-functionalinternal and ...
Strongknowledge of data management best practices & technologies as applied to clinical trials. * Excellent communication and interpersonal skills to collaborate with cross-functionalinternal and ...
Report project status and escalate study-related issues to senior leadership Requirements: * Bachelor of Science degree with 10+ years of clinical data management experience * Proficiency in EDC ...
Report project status and escalate study-related issues to senior leadership Requirements: * Bachelor of Science degree with 10+ years of clinical data management experience * Proficiency in EDC ...
Durham, NC · On-site +1
Strong knowledge of data management best practices & technologies as applied to clinical trials. * Excellent communication and interpersonal skills to collaborate with cross-functional internal and ...
Durham, NC · On-site +1
Strong knowledge of data management best practices & technologies as applied to clinical trials. * Excellent communication and interpersonal skills to collaborate with cross-functional internal and ...
In this role as a Senior Clinical Data Manager II, you will be responsible for coordination of the Clinical Data Management (CDM) deliverables on assigned clinical studies and may be an expert on CDM ...
In this role as a Senior Clinical Data Manager II, you will be responsible for coordination of the Clinical Data Management (CDM) deliverables on assigned clinical studies and may be an expert on CDM ...
In this role as a Senior Clinical Data Manager II, you will be responsible for coordination of the Clinical Data Management (CDM) deliverables on assigned clinical studies and may be an expert on CDM ...
In this role as a Senior Clinical Data Manager II, you will be responsible for coordination of the Clinical Data Management (CDM) deliverables on assigned clinical studies and may be an expert on CDM ...
Palo Alto, CA · On-site
$130K/yr
Senior Clinical Data Manager Role Overview The Senior Clinical Data Manager will play a critical role in database development, data quality oversight, and vendor coordination to ensure accurate ...
Palo Alto, CA · On-site
$130K/yr
Senior Clinical Data Manager Role Overview The Senior Clinical Data Manager will play a critical role in database development, data quality oversight, and vendor coordination to ensure accurate ...
In this role as a Senior Clinical Data Manager II, you will be responsible for coordination of the Clinical Data Management (CDM) deliverables on assigned clinical studies and may be an expert on CDM ...
In this role as a Senior Clinical Data Manager II, you will be responsible for coordination of the Clinical Data Management (CDM) deliverables on assigned clinical studies and may be an expert on CDM ...
In this role as a Senior Clinical Data Manager II, you will be responsible for coordination of the Clinical Data Management (CDM) deliverables on assigned clinical studies and may be an expert on CDM ...
In this role as a Senior Clinical Data Manager II, you will be responsible for coordination of the Clinical Data Management (CDM) deliverables on assigned clinical studies and may be an expert on CDM ...
Clinical Data Manager will be responsible for all aspects of clinical trial data management from study start up through database lock and study close. * This includes the EDC build and user ...
Clinical Data Manager will be responsible for all aspects of clinical trial data management from study start up through database lock and study close. * This includes the EDC build and user ...
Clinical Data Manager will be responsible for all aspects of clinical trial data management from study start up through database lock and study close * This includes the EDC build and user acceptance ...
Clinical Data Manager will be responsible for all aspects of clinical trial data management from study start up through database lock and study close * This includes the EDC build and user acceptance ...
Princeton, NJ · On-site
Clinical Data Management Leader Provide leadership, strategic planning, direction and implementation of clinical systems for data collection which may include vendor selection, budgeting, resource ...
Princeton, NJ · On-site
Clinical Data Management Leader Provide leadership, strategic planning, direction and implementation of clinical systems for data collection which may include vendor selection, budgeting, resource ...
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 ...
Support Lead Clinical Programmers in developing and managing Data Transfer Agreements. * Lead regular data review across studies, identifying quality issues, trends, and outliers, and generate ...
Support Lead Clinical Programmers in developing and managing Data Transfer Agreements. * Lead regular data review across studies, identifying quality issues, trends, and outliers, and generate ...
Lead all data management (DM) activities for one or more clinical trials. * Contribute to developing study protocols, statistical analysis plans, and clinical study reports. * Collaborate with ...
Lead all data management (DM) activities for one or more clinical trials. * Contribute to developing study protocols, statistical analysis plans, and clinical study reports. * Collaborate with ...
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 ...
What are the key skills and qualifications needed to thrive as a Senior Clinical Data Manager, and why are they important?
How does a Senior Clinical Data Manager typically collaborate with cross-functional teams during a clinical trial?
What does a Senior Clinical Data Manager do?
What is the difference between Senior Clinical Data Manager vs Clinical Data Coordinator?
| Aspect | Senior Clinical Data Manager | Clinical Data Coordinator |
|---|---|---|
| Credentials | Bachelor's/Master's in Life Sciences, Biostatistics, or related field; experience in data management | Bachelor's degree in Life Sciences or related field; entry-level experience |
| Work Environment | Leads data management teams, oversees data quality, and ensures compliance | Supports data entry, validation, and basic data queries |
| Industry Usage | Used in pharmaceutical, biotech, and clinical research organizations | Common in clinical trial sites and research organizations |
The Senior Clinical Data Manager typically has more experience, oversees data management processes, and ensures data quality, while the Clinical Data Coordinator handles data entry and validation tasks. Both roles are essential in clinical research but differ in responsibility level and scope.
What is it like to work at Regeneron?
Do workers at Regeneron get paid breaks?
Does Regeneron pay people when they’re sick?
At Regeneron, are sick days and vacation days separate paid time off?
Is the health insurance from Regeneron affordable enough for their workers?
Do people get paid time off at Regeneron?
Do workers at Regeneron worry about hours?
Do Regeneron workers get to choose the shifts they work?
How easy is it for Regeneron workers to change shifts?
How easy is it to get time off at Regeneron?
Do Regeneron managers change schedules at the last minute?
Do workers at Regeneron do extra work that they don't get paid for?
How easy is it to take sick days at Regeneron?
Do people at Regeneron feel treated with respect by their managers?
Do people at Regeneron get to take their breaks without interruption?
Is it stressful to work at Regeneron?
Do people at Regeneron enjoy their jobs?
Do people at Regeneron recommend working with their team?
Do people get enough training when they start at Regeneron?
Do people get support to advance at Regeneron?
Do people think Regeneron’s headquarters understands what’s happening where they work?
Do workers feel well informed about how Regeneron is doing?

Full-time
Posted 24 days ago
Who we are
We're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way.
Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.
Why Worldwide
We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day.Join us!
What the Senior Clinical Data Manager does at Worldwide
Oversee, lead, manage, and provide technicalexpertisewithin the assigned projects to ensure that they are executed in an efficient,accurate, andtimelymanner to the Sponsor's satisfaction.
What you will do
Provide fully independent and autonomous leadership of data management services (start up, conduct, and close out) across multiple complex globalprojects/programs, including:
Ensureappropriateresourcesareallocatedto complete all DM activities on time and within budget.
Prepare DM trial documentation (DMP, DB Specifications, Edit check specifications, CCGs, DTAs).
Ensure effective UAT is performed.
Write external vendor reconciliation specifications for programming reconciliation outputs (e.g. Serious Adverse Events, IRT, Central Laboratory).
Oversee data cleaning activities.
Produce metrics tomonitorprogress of trial activities.
Ensure alldatabaselock activities are completed on time.
Represent WorldWideDM at both internal and external study meeting calls, including providing input.
Monitor project scope, budgets and risks and alert DM Management of any concerns.
Liaise with DM Management at regular intervals to discuss progress and any issues outstanding (e.g. during Project Review Meetings).
Collaborate with internal Worldwidedepartments working on the same project.
Provide feedback on process improvements to DM Management and/or SMEs.
Participate in and lead process reviews.
Provide training,support, and mentorship to other members of the DM department.
Participate as necessary in sponsor audits, regulatory authority inspections, and otherthird-partymeetings.
Perform other duties as assigned.The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.
What you bring to the role
Excellent attention to detail.
Excellent written and verbal communication skills.
Strongknowledge of data management best practices & technologies as applied to clinical trials.
Excellent communication and interpersonal skills to collaborate with cross-functionalinternal and external teams.
Strongunderstanding of clinical trial process and protocols documents (protocols, statistical analysis plans, CRFs, study reports) and processes.
Stronganalytical andproblem-solvingskills.
Independent and autonomous project oversight skills.
Your experience
Bachelor's degree or higher in biomedical sciences, life sciences, computerscience, or related discipline - or equivalent relevant experience.
Min of 5 years of experience in clinical data management or a related role within the pharmaceutical, biotechnology, or medical device industries.
Promotion to the next level is not automatic based on years of experience. Personnel are evaluated on proven competency, level of responsibility, and ability to work independently.
We love knowing that someone is going to have a better life because of the work we do.
To view our other roles, check out our careers page at Discover a world of difference at Worldwide!For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.
Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative,innovative,and successful. We'reon a mission to hire thevery bestand are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.
Sourced by ZipRecruiter
Scientific research and development services
10,000+ Employees
Durham, NC, US
1986