Maintain accurate pipeline management and forecasting in CRM systems, with attention to evidence project cycles, platform usage models, and customer expansion opportunities. * Drive Growth: Identify ...
Maintain accurate pipeline management and forecasting in CRM systems, with attention to evidence project cycles, platform usage models, and customer expansion opportunities. * Drive Growth: Identify ...
Case Investigation & Evidence Management * Coordinate deep-dive case investigations and track critical evidence. * Manage complex medical record reviews, organization, and tracking. * Maintain hyper ...
New
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Case Investigation & Evidence Management * Coordinate deep-dive case investigations and track critical evidence. * Manage complex medical record reviews, organization, and tracking. * Maintain hyper ...
New
Associate Principal, Indirect Treatment Comparison (ITC), Evidence Synthesis
Greenwich, CT · Remote
$125K - $350K/yr
Project management-manage projects, oversee the operational, financial, and administrative ... evidence synthesis research in a pharma consulting environment Minimum required : * Master's in ...
Associate Principal, Indirect Treatment Comparison (ITC), Evidence Synthesis
Greenwich, CT · Remote
$125K - $350K/yr
Project management-manage projects, oversee the operational, financial, and administrative ... evidence synthesis research in a pharma consulting environment Minimum required : * Master's in ...
Associate Principal, Indirect Treatment Comparison (ITC), Evidence Synthesis
Greenwich, CT · Remote
$125K - $350K/yr
Project management-manage projects, oversee the operational, financial, and administrative ... evidence synthesis research in a pharma consulting environment Minimum required : * Master's in ...
Associate Principal, Indirect Treatment Comparison (ITC), Evidence Synthesis
Greenwich, CT · Remote
$125K - $350K/yr
Project management-manage projects, oversee the operational, financial, and administrative ... evidence synthesis research in a pharma consulting environment Minimum required : * Master's in ...
... evidence management. Essential Duties and Responsibilities * Program Ownership: Build, optimize, and maintain on-site processes and documentation to ensure continuous adherence to NERC CIP standards.
... evidence management. Essential Duties and Responsibilities * Program Ownership: Build, optimize, and maintain on-site processes and documentation to ensure continuous adherence to NERC CIP standards.
... evidence management. Essential Duties and Responsibilities * Program Ownership: Build, optimize, and maintain on-site processes and documentation to ensure continuous adherence to NERC CIP standards.
... evidence management. Essential Duties and Responsibilities * Program Ownership: Build, optimize, and maintain on-site processes and documentation to ensure continuous adherence to NERC CIP standards.
... evidence management. Essential Duties and Responsibilities * Program Ownership: Build, optimize, and maintain on-site processes and documentation to ensure continuous adherence to NERC CIP standards.
... evidence management. Essential Duties and Responsibilities * Program Ownership: Build, optimize, and maintain on-site processes and documentation to ensure continuous adherence to NERC CIP standards.
... evidence management. Essential Duties and Responsibilities * Program Ownership: Build, optimize, and maintain on-site processes and documentation to ensure continuous adherence to NERC CIP standards.
... evidence management. Essential Duties and Responsibilities * Program Ownership: Build, optimize, and maintain on-site processes and documentation to ensure continuous adherence to NERC CIP standards.
Testing/validation and evidence management for audit/exams * Understanding of investment management operational functions (e.g., trade operations, investment accounting, performance and attribution ...
Testing/validation and evidence management for audit/exams * Understanding of investment management operational functions (e.g., trade operations, investment accounting, performance and attribution ...
Senior NERC CIP Compliance Analyst
New Haven, CT · On-site
$130K - $160K/yr
... evidence management. Essential Duties and Responsibilities * Program Ownership: Build, optimize, and maintain on-site processes and documentation to ensure continuous adherence to NERC CIP standards.
Senior NERC CIP Compliance Analyst
New Haven, CT · On-site
$130K - $160K/yr
... evidence management. Essential Duties and Responsibilities * Program Ownership: Build, optimize, and maintain on-site processes and documentation to ensure continuous adherence to NERC CIP standards.
Senior NERC CIP Compliance Analyst
Middletown, CT · On-site
$130K - $160K/yr
... evidence management. Essential Duties and Responsibilities * Program Ownership: Build, optimize, and maintain on-site processes and documentation to ensure continuous adherence to NERC CIP standards.
Senior NERC CIP Compliance Analyst
Middletown, CT · On-site
$130K - $160K/yr
... evidence management. Essential Duties and Responsibilities * Program Ownership: Build, optimize, and maintain on-site processes and documentation to ensure continuous adherence to NERC CIP standards.
You will work closely with our team of experts to ensure that our program is evidence-based ... Experience with grant writing and management * Experience with program evaluation and quality ...
New
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You will work closely with our team of experts to ensure that our program is evidence-based ... Experience with grant writing and management * Experience with program evaluation and quality ...
New
Global Medical Affairs Operations Manager
Bridgeport, CT · On-site
$140K/yr
Global Medical Affairs Operations Manager Medela LLC Salary starting at $140K Travel 30% Maternal ... Develop evidence-based materials, case studies, and customer success stories highlighting clinical ...
New
Global Medical Affairs Operations Manager
Bridgeport, CT · On-site
$140K/yr
Global Medical Affairs Operations Manager Medela LLC Salary starting at $140K Travel 30% Maternal ... Develop evidence-based materials, case studies, and customer success stories highlighting clinical ...
New
Regulatory Affairs Manager
Westport, CT · On-site
$100K - $110K/yr
Regulatory Affairs Manager Quality Department Reports to the Sr. Manager 19 Newtown Turnpike ... Our technology is backed by clinical evidence and real-world results, helping patients reduce pain ...
Quick apply
Regulatory Affairs Manager
Westport, CT · On-site
$100K - $110K/yr
Regulatory Affairs Manager Quality Department Reports to the Sr. Manager 19 Newtown Turnpike ... Our technology is backed by clinical evidence and real-world results, helping patients reduce pain ...
Promote evidence-based practice, quality, and patient safety initiatives * Serve as a clinical resource and mentor to RNs and charge nurses * Support staffing coordination and shift-to-shift ...
Promote evidence-based practice, quality, and patient safety initiatives * Serve as a clinical resource and mentor to RNs and charge nurses * Support staffing coordination and shift-to-shift ...
Promote evidence-based practice, quality, and patient safety initiatives * Serve as a clinical resource and mentor to RNs and charge nurses * Support staffing coordination and shift-to-shift ...
Promote evidence-based practice, quality, and patient safety initiatives * Serve as a clinical resource and mentor to RNs and charge nurses * Support staffing coordination and shift-to-shift ...
VP, Information Lifecycle Management Program Manager
Stamford, CT · On-site +1
$123K - $124K/yr
Support audits and regulatory inquiries by providing evidence of controls, policy adherence, and ... manager and HR if you don't meet the time in position or performance expectations). Legal ...
VP, Information Lifecycle Management Program Manager
Stamford, CT · On-site +1
$123K - $124K/yr
Support audits and regulatory inquiries by providing evidence of controls, policy adherence, and ... manager and HR if you don't meet the time in position or performance expectations). Legal ...
VP, Information Lifecycle Management Program Manager
Stamford, CT · On-site +1
$123K - $124K/yr
Support audits and regulatory inquiries by providing evidence of controls, policy adherence, and ... manager and HR if you don't meet the time in position or performance expectations). Legal ...
VP, Information Lifecycle Management Program Manager
Stamford, CT · On-site +1
$123K - $124K/yr
Support audits and regulatory inquiries by providing evidence of controls, policy adherence, and ... manager and HR if you don't meet the time in position or performance expectations). Legal ...
Program Manager
New Haven, CT · On-site
$65K - $69K/yr
Oversee and manage all aspects of the implementation of evidence-based models within program service delivery , including but not limited to Critical Time Intervention (CTI), Motivational ...
Quick apply
Program Manager
New Haven, CT · On-site
$65K - $69K/yr
Oversee and manage all aspects of the implementation of evidence-based models within program service delivery , including but not limited to Critical Time Intervention (CTI), Motivational ...
Program Manager
New Haven, CT · On-site
Oversee and manage all aspects of the implementation of evidence-based models within program service delivery , including but not limited to Critical Time Intervention (CTI), Motivational ...
Program Manager
New Haven, CT · On-site
Oversee and manage all aspects of the implementation of evidence-based models within program service delivery , including but not limited to Critical Time Intervention (CTI), Motivational ...
Evidence Manager information
What is the difference between Evidence Manager vs Forensic Analyst?
| Aspect | Evidence Manager | Forensic Analyst |
|---|---|---|
| Credentials | Typically requires a bachelor's degree in criminal justice, forensic science, or related field; certifications like Certified Evidence Specialist (CES) are common | Requires a degree in forensic science, chemistry, or biology; certifications such as Certified Forensic Scientist (CFS) are often preferred |
| Work Environment | Manages evidence storage, documentation, and chain of custody in law enforcement or legal settings | Analyzes physical and digital evidence in labs or crime scene investigations |
| Employer & Industry | Law enforcement agencies, legal firms, government labs | Crime labs, law enforcement agencies, private forensic firms |
While both Evidence Managers and Forensic Analysts work within the criminal justice system, Evidence Managers focus on organizing and maintaining evidence, ensuring its integrity. Forensic Analysts, on the other hand, perform scientific analysis of evidence to support investigations. Both roles require specialized certifications and work in related environments, but their core responsibilities differ significantly.
What are some common challenges faced by evidence managers, and how can they effectively address them?
What is an evidence manager?
What are the key skills and qualifications needed to thrive as an evidence manager, and why are they important?
What are popular job titles related to Evidence Manager jobs in Connecticut?
For Evidence Manager jobs in Connecticut, the most frequently searched job titles are:
What job categories do people searching Evidence Manager jobs in Connecticut look for?
The top searched job categories for Evidence Manager jobs in Connecticut are:
What cities in Connecticut are hiring for Evidence Manager jobs?
Cities in Connecticut with the most Evidence Manager job openings:
Datavant rating
7.1
Based on 103 frontline employees who took The Breakroom Quiz
149th of 224 rated it services
Job description
Datavant is the data collaboration platform trusted for healthcare. Guided by our mission to make the world's health data secure, accessible and actionable, we provide critical data solutions for organizations across the healthcare ecosystem - including providers, health plans, researchers, and life sciences companies. From fulfilling a single patient's request for their medical records to powering the AI revolution in healthcare, Datavanters are building the future of how data is connected and used to improve health.
By joining Datavant today, you're stepping onto a driven and highly collaborative team that is passionate about creating transformative change in healthcare.
Objective of the Role
The Client Partner, Real-World Evidence is responsible for driving growth with biopharma customers by leveraging Datavant's portfolio of real-world evidence (RWE) solutions, analytics platforms, and AI platform and services. This role will partner closely with Client Partners across key accounts for co-selling, account planning, and evidence strategy alignment.
You will serve as a trusted advisor on the use of real-world data (RWD) and RWE to support regulatory, market access, and HEOR needs - representing the voice of the customer and ensuring that Datavant's offerings meet evolving evidence generation requirements. The ideal candidate is comfortable leading complex, multi-stakeholder sales cycles and brings deep expertise in real-world data, evidence platforms, and outcomes research.
Responsibilities of the Role
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Prospect & Generate Leads: Develop and execute strategic plans to identify and target new business opportunities in biopharma, healthcare, and life sciences with a focus on organizations investing in real-world evidence strategies for regulatory submissions, market access, and clinical development.
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Build Pipeline: Proactively engage prospects via outbound calls, emails, and industry networking to build a robust pipeline of opportunities related to Aetion's evidence generation, AI, and analytics solutions.
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Close Deals: Own the full sales process - from initial outreach to contract closure - ensuring alignment between customer evidence needs and Aetion's RWE offerings, including the Aetion Evidence Platform (AEP) and associated data and consulting services.
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Client Engagement: Present Aetion's value proposition in RWE and RWD analytics through compelling demonstrations and business cases that highlight regulatory-grade evidence generation, comparative effectiveness, and real-world outcomes research. Engage with senior stakeholders including heads of HEOR, RWE, Market Access, and Clinical Development.
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Collaborate Cross-Functionally: Partner with marketing, product, and science teams to deliver tailored RWE solution proposals, ensuring alignment with client data strategies, evidence frameworks, and regulatory expectations (e.g., FDA, EMA guidance).
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Market Expertise: Stay current on RWE market dynamics, technology and AI, regulatory guidance for real-world data, and competitor offerings to position Aetion as a strategic leader and partner of choice in the evidence generation ecosystem.
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Forecasting & Reporting: Maintain accurate pipeline management and forecasting in CRM systems, with attention to evidence project cycles, platform usage models, and customer expansion opportunities.
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Drive Growth: Identify new and upsell opportunities across assigned territories and existing accounts, particularly in expanding RWE adoption for post-approval studies, safety monitoring, and market access support.
Qualifications of the Role
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Proven Track Record: 6+ years of successful sales experience, ideally in healthcare, life sciences, or SaaS; with a strong preference for experience selling RWE, HEOR, or data analytics solutions. Background in selling AI is also to be considered.
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RWE Expertise: Deep understanding of real-world data sources, evidence generation methodologies, and use cases across the product lifecycle - from clinical development to commercialization.
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Hunter Mentality: Skilled at identifying, developing, and closing new RWE-focused opportunities with top biopharma clients.
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Sales Expertise: Experience managing complex, consultative sales cycles involving scientific, commercial, and data stakeholders.
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Technology/AI Skill Sets: Proven experience, knowledge, and market understanding on real AI-driven use cases for HEOR and RWE.
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Presentation Skills: Exceptional ability to communicate scientific and technical value propositions to diverse audiences, including C-suite and RWE/HEOR leadership.
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CRM Proficiency: Experienced in CRM management for tracking RWE opportunity pipelines and forecasting revenue growth.
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Industry Knowledge: In-depth knowledge of RWE market trends, regulatory guidance, and payer evidence needs is essential.
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Collaborative Team Player: Comfortable working with cross-functional science, data, and product teams in a fast-paced, mission-driven environment.
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Communication Skills: Strong written and verbal communication skills, capable of translating complex RWE concepts into impactful narratives for decision-makers.
#BC-LI1
We are committed to building a diverse team of Datavanters who are all responsible for stewarding a high-performance culture in which all Datavanters belong and thrive. We are proud to be an Equal Employment Opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, or other legally protected status.
At Datavant our total rewards strategy powers a high-growth, high-performance, health technology company that rewards our employees for transforming health care through creating industry-defining data logistics products and services.
The range posted is for a given job title, which can include multiple levels. Individual rates for the same job title may differ based on their level, responsibilities, skills, and experience for a specific job. This role is eligible for additional variable compensation.
The estimated base salary range (not including variable pay) for this role is:
$140,000-$170,000 USD
To ensure the safety of patients and staff, many of our clients require post-offer health screenings and proof and/or completion of various vaccinations such as the flu shot, Tdap, COVID-19, etc. Any requests to be exempted from these requirements will be reviewed by Datavant Human Resources and determined on a case-by-case basis. Depending on the state in which you will be working, exemptions may be available on the basis of disability, medical contraindications to the vaccine or any of its components, pregnancy or pregnancy-related medical conditions, and/or religion.
This job is not eligible for employment sponsorship.
Datavant is committed to a work environment free from job discrimination. We are proud to be an Equal Employment Opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, or other legally protected status. To learn more about our commitment, please review our EEO Commitment Statement here (https://www.datavant.com/eeo-commitment-statement) . Know Your Rights (https://www.eeoc.gov/know-your-rights-workplace-discrimination-illegal) , explore the resources available through the EEOC for more information regarding your legal rights and protections. In addition, Datavant does not and will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay.
At the end of this application, you will find a set of voluntary demographic questions. If you choose to respond, your answers will be anonymous and will help us identify areas for improvement in our recruitment process. (We can only see aggregate responses, not individual ones. In fact, we aren't even able to see whether you've responded.) Responding is entirely optional and will not affect your application or hiring process in any way.
Datavant is committed to working with and providing reasonable accommodations to individuals with physical and mental disabilities. If you need an accommodation while seeking employment, please request it here, (https://peopleteam.datavant.com/portal/en/newticket?departmentId=248697000248790029&layoutId=248697000248795462) by selecting the 'Interview Accommodation Request' category. You will need your requisition ID when submitting your request, you can find instructions for locating it here (https://app.tango.us/app/workflow/Greenhouse--Locating-Requisition-ID-2c7d618c8a8a423da4330ff12330695e) . Requests for reasonable accommodations will be reviewed on a case-by-case basis.
For more information about how we collect and use your data, please review our Privacy Policy (https://www.datavant.com/privacy-policy) .
About Datavant
Sourced by ZipRecruiter
Industry
Software development
Company size
51 - 200 Employees
Headquarters location
San Francisco, CA, US
Year founded
2017