... VEEVA Assist in UAT testing Minimum education requirements: Bachelor's degree in a related field ... Clinical Supplies QA/Regulatory Precision Medicine Supply Chain Manufacturing Procurement Or ...
... VEEVA Assist in UAT testing Minimum education requirements: Bachelor's degree in a related field ... Clinical Supplies QA/Regulatory Precision Medicine Supply Chain Manufacturing Procurement Or ...
Sr. Clinical Research Associate
Wyoming, MI · On-site +1
Utilize and maintain accurate study data in clinical systems, including Veeva Vault CTMS and CDMS. * Work crossfunctionally with internal teams and CROs to ensure highquality study execution and ...
Sr. Clinical Research Associate
Wyoming, MI · On-site +1
Utilize and maintain accurate study data in clinical systems, including Veeva Vault CTMS and CDMS. * Work crossfunctionally with internal teams and CROs to ensure highquality study execution and ...
Utilize and maintain accurate study data in clinical systems, including Veeva Vault CTMS and CDMS. * Work crossfunctionally with internal teams and CROs to ensure highquality study execution and ...
Utilize and maintain accurate study data in clinical systems, including Veeva Vault CTMS and CDMS. * Work crossfunctionally with internal teams and CROs to ensure highquality study execution and ...
Senior Nonclinical Writer (US)
Canton, MI · On-site
Ability to work in various client systems (eg, SharePoint, Veeva RIM, PleaseReview, EndNote), templates and toolbars. * Strong understanding of regulatory guidances as it applies to nonclinical ...
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Senior Nonclinical Writer (US)
Canton, MI · On-site
Ability to work in various client systems (eg, SharePoint, Veeva RIM, PleaseReview, EndNote), templates and toolbars. * Strong understanding of regulatory guidances as it applies to nonclinical ...
Senior Nonclinical Writer (US)
Canton, MI · On-site
Ability to work in various client systems (eg, SharePoint, Veeva RIM, PleaseReview, EndNote), templates and toolbars. * Strong understanding of regulatory guidances as it applies to nonclinical ...
Senior Nonclinical Writer (US)
Canton, MI · On-site
Ability to work in various client systems (eg, SharePoint, Veeva RIM, PleaseReview, EndNote), templates and toolbars. * Strong understanding of regulatory guidances as it applies to nonclinical ...
You will partner closely with Clinical Data Management, CROs, external vendors, and cross ... Veeva, or Oracle Inform * Experience working with SAS, CSV, and XML data formats * Strong ...
You will partner closely with Clinical Data Management, CROs, external vendors, and cross ... Veeva, or Oracle Inform * Experience working with SAS, CSV, and XML data formats * Strong ...
Global Medical Affairs Operations Manager
Grand Rapids, MI · On-site
$140K/yr
This role is a critical connector across Medical Affairs, Clinical, Sales, Marketing, and external ... Experience with platforms such as Salesforce, SAP, Veeva, or KOL management tools is a plus
Global Medical Affairs Operations Manager
Grand Rapids, MI · On-site
$140K/yr
This role is a critical connector across Medical Affairs, Clinical, Sales, Marketing, and external ... Experience with platforms such as Salesforce, SAP, Veeva, or KOL management tools is a plus
This role is a critical connector across Medical Affairs, Clinical, Sales, Marketing, and external ... Experience with platforms such as Salesforce, SAP, Veeva, or KOL management tools is a plus
This role is a critical connector across Medical Affairs, Clinical, Sales, Marketing, and external ... Experience with platforms such as Salesforce, SAP, Veeva, or KOL management tools is a plus
The MSL's key objective is to create impact through advancing clinical practice within the assigned ... Execute all administrative responsibilities and training (e.g., Veeva CRM, voicemail, e-mail ...
The MSL's key objective is to create impact through advancing clinical practice within the assigned ... Execute all administrative responsibilities and training (e.g., Veeva CRM, voicemail, e-mail ...
The MSL's key objective is to create impact through advancing clinical practice within the assigned ... Execute all administrative responsibilities and training (e.g., Veeva CRM, voicemail, e-mail ...
The MSL's key objective is to create impact through advancing clinical practice within the assigned ... Execute all administrative responsibilities and training (e.g., Veeva CRM, voicemail, e-mail ...
The MSL's key objective is to create impact through advancing clinical practice within the assigned ... Execute all administrative responsibilities and training (e.g., Veeva CRM, voicemail, e-mail ...
The MSL's key objective is to create impact through advancing clinical practice within the assigned ... Execute all administrative responsibilities and training (e.g., Veeva CRM, voicemail, e-mail ...
The MSL's key objective is to create impact through advancing clinical practice within the assigned ... Execute all administrative responsibilities and training (e.g., Veeva CRM, voicemail, e-mail ...
The MSL's key objective is to create impact through advancing clinical practice within the assigned ... Execute all administrative responsibilities and training (e.g., Veeva CRM, voicemail, e-mail ...
The MSL's key objective is to create impact through advancing clinical practice within the assigned ... Execute all administrative responsibilities and training (e.g., Veeva CRM, voicemail, e-mail ...
The MSL's key objective is to create impact through advancing clinical practice within the assigned ... Execute all administrative responsibilities and training (e.g., Veeva CRM, voicemail, e-mail ...
The MSL's key objective is to create impact through advancing clinical practice within the assigned ... Execute all administrative responsibilities and training (e.g., Veeva CRM, voicemail, e-mail ...
The MSL's key objective is to create impact through advancing clinical practice within the assigned ... Execute all administrative responsibilities and training (e.g., Veeva CRM, voicemail, e-mail ...
The MSL's key objective is to create impact through advancing clinical practice within the assigned ... Execute all administrative responsibilities and training (e.g., Veeva CRM, voicemail, e-mail ...
The MSL's key objective is to create impact through advancing clinical practice within the assigned ... Execute all administrative responsibilities and training (e.g., Veeva CRM, voicemail, e-mail ...
The MSL's key objective is to create impact through advancing clinical practice within the assigned ... Execute all administrative responsibilities and training (e.g., Veeva CRM, voicemail, e-mail ...
The MSL's key objective is to create impact through advancing clinical practice within the assigned ... Execute all administrative responsibilities and training (e.g., Veeva CRM, voicemail, e-mail ...
The MSL's key objective is to create impact through advancing clinical practice within the assigned ... Execute all administrative responsibilities and training (e.g., Veeva CRM, voicemail, e-mail ...
The MSL's key objective is to create impact through advancing clinical practice within the assigned ... Execute all administrative responsibilities and training (e.g., Veeva CRM, voicemail, e-mail ...
Medical Science Liaison Onc Prostate Radioligand Therapies Michigan Territory
Ann Arbor, MI · On-site
$158K - $237K/yr
The MSL's key objective is to create impact through advancing clinical practice within the assigned ... Veeva CRM, voicemail, e-mail, expense reports, compliance modules, etc.) in a timely manner ...
Medical Science Liaison Onc Prostate Radioligand Therapies Michigan Territory
Ann Arbor, MI · On-site
$158K - $237K/yr
The MSL's key objective is to create impact through advancing clinical practice within the assigned ... Veeva CRM, voicemail, e-mail, expense reports, compliance modules, etc.) in a timely manner ...
The MSL's key objective is to create impact through advancing clinical practice within the assigned ... Veeva CRM, voicemail, e-mail, expense reports, compliance modules, etc.) in a timely manner ...
The MSL's key objective is to create impact through advancing clinical practice within the assigned ... Veeva CRM, voicemail, e-mail, expense reports, compliance modules, etc.) in a timely manner ...
Medical Science Liaison Onc Prostate Radioligand Therapies Michigan Territory
Detroit, MI · On-site
$158K - $237K/yr
The MSL's key objective is to create impact through advancing clinical practice within the assigned ... Veeva CRM, voicemail, e-mail, expense reports, compliance modules, etc.) in a timely manner ...
Medical Science Liaison Onc Prostate Radioligand Therapies Michigan Territory
Detroit, MI · On-site
$158K - $237K/yr
The MSL's key objective is to create impact through advancing clinical practice within the assigned ... Veeva CRM, voicemail, e-mail, expense reports, compliance modules, etc.) in a timely manner ...
Veeva Clinical information
What is a Veeva Clinical professional?
A Veeva Clinical professional is someone who specializes in using the Veeva Vault Clinical Suite, a cloud-based platform designed to manage clinical trial processes and data in the life sciences industry. Their responsibilities often include implementing, configuring, and supporting Veeva Vault Clinical applications such as eTMF, CTMS, and Study Startup. These professionals help organizations streamline clinical operations, ensure regulatory compliance, and improve collaboration across trial teams. Their expertise is highly valued by pharmaceutical, biotech, and contract research organizations.
What are the key skills and qualifications needed to thrive as a Veeva Clinical specialist?
To thrive as a Veeva Clinical Specialist, you need a solid understanding of clinical trial processes, data management, and life sciences regulations, often supported by a degree in life sciences or related fields. Familiarity with Veeva Vault Clinical Suite, electronic data capture (EDC) systems, and relevant certifications like Veeva Vault Administrator are highly valued. Strong analytical thinking, attention to detail, and effective communication are essential soft skills for collaborating with cross-functional teams and clients. These competencies ensure the optimization of clinical workflows, regulatory compliance, and successful implementation of Veeva solutions in clinical research environments.
What are some common challenges faced by professionals working in Veeva Clinical roles, and how can they be addressed?
Professionals in Veeva Clinical roles often encounter challenges such as adapting to frequent software updates, ensuring data integrity across multiple studies, and coordinating with cross-functional teams like clinical operations and IT. Staying current with new features and best practices is essential to maximize the platform's capabilities. Proactive communication and ongoing training can help address these challenges, as well as building strong relationships with stakeholders to streamline workflows and resolve issues efficiently.
What are popular job titles related to Veeva Clinical jobs in Michigan?
For Veeva Clinical jobs in Michigan, the most frequently searched job titles are:
What job categories do people searching Veeva Clinical jobs in Michigan look for?
The top searched job categories for Veeva Clinical jobs in Michigan are:
What cities in Michigan are hiring for Veeva Clinical jobs?
Cities in Michigan with the most Veeva Clinical job openings:
Clinical Supply Support Specialist Services - FSP
Three Rivers, MI • On-site
Parexel •
Pharmaceutical and Medicine Manufacturing • 10K+ employees10,000+ employees
8.2
Based on 13 frontline employees who took The Breakroom Quiz
31st of 74 rated research
Great coworkers
People enjoy working here
Good employer
Good schedule notice
Respectful managers
Full-time
Re-posted 3 days ago
Job description
When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
Parexel FSP is hiring multiple Clinical Supply Support Specialist positions. The position will be office-based in Warren, New Jersey.
Clinical Supply & Inventory Planning & Execution
Supply monitoring, assessment and oversight activities (risks, stocking levels, trends)
Pull relevant data for metrics reporting & maintain metrics
Process requisitions and ensure timely procurement of comparator drugs & ancillary supplies
Track and manage comparator documentation updates
Clinical Supply Shipments
Initiate non-system generated shipments
Monitor and track comparator drug delivery schedules
Coordinate Depot transfers & site return shipments
Temperature excursion management and resolution
Clinical Supply Monitoring & Activity Documentation (Electronic Trial Master File - eTMF)
Expected Document List (EDL) creation
Update comparator IMN (Item Master Number)
Update and maintain eTMF Document Management per regulatory requirements Request QA/QP Releases
Pack-and-label kit and sequence reconciliation
Inspection Readiness activities
IRT management activities, including IRT Alert management and UAT activities
IP / Ancillary Supplies Compatibility Review
Receive and triage request, forward to FDG for review
Perform internet searches and contact manufacturers for information
Data entry of information into database (ASIST or spreadsheet) and Teams
Clinical Supply Systems
Manage CSS Email Inbox
Manage IRT system access for users for all studies
Complete EDL, IRR and StiL reviews every 3 months for all studies
Manage all TMF documentation uploads into VEEVA
Assist in UAT testing
Minimum education requirements:
Bachelor's degree in a related field with an internship or prior industry work experience.
Preferred 2+ years of experience in the following fields:
Clinical Supplies
QA/Regulatory Precision Medicine
Supply Chain Manufacturing
Procurement
Or equivalent research/commercial biopharma experience
EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
About PAREXEL
Sourced by ZipRecruiter
Bring your Data Management expertise to Parexel's Strategic Partnerships. Although we work globally, each partnership we form is deeply personal. We are as dedicated to every aspect of our client's product development as they are - and work closely with client teams in true partnership to understand both challenges and opportunities. At Parexel we are focused on meeting customer and patient needs through collaborative partnership so that we get treatments into the hands of patients who need them most.
Industry
Pharmaceutical and medicine manufacturing
Company size
10,000+ Employees
Headquarters location
Waltham, MA, US
Year founded
1983
