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Eclinical Jobs (NOW HIRING)

eClinical Solutions

Principal Software Engineer

Mansfield, MA · On-site +1

$142K - $191K/yr

About eClinical Solutions eClinical Solutions is transforming clinical development with elluminate ® , our Clinical Data Cloud , helping life sciences organizations unify, analyze, and unlock the ...

eClinical Solutions

Principal Software Engineer

Mansfield, MA · On-site +1

$142K - $191K/yr

About eClinical Solutions eClinical Solutions is transforming clinical development with elluminate, our Clinical Data Cloud , helping life sciences organizations unify, analyze, and unlock the value ...

eClinical Solutions

Principal Software Engineer

Mansfield, MA · On-site +1

$142K - $191K/yr

About eClinical Solutions eClinical Solutions is transforming clinical development with elluminate ® , our Clinical Data Cloud , helping life sciences organizations unify, analyze, and unlock the ...

eClinical Solutions

Technical Project Manager

OR · Remote

eClinical Solutions helps life sciences organizations around the world accelerate clinical development initiatives with expert data services and the elluminate Clinical Data Cloud - the foundation of ...

eClinical Solutions

Principal Software Engineer

Mansfield, MA · On-site +1

$142K - $191K/yr

About eClinical Solutions eClinical Solutions is transforming clinical development with elluminate, our Clinical Data Cloud , helping life sciences organizations unify, analyze, and unlock the value ...

eClinical Solutions

Senior Software Engineer

$125K - $165K/yr

Job Summary : eClinical Solutions is transforming clinical development with elluminate ® , their Clinical Data Cloud that helps life sciences organizations unify, analyze, and unlock the value of ...

eClinical Solutions

Principal Software Engineer

Mansfield, MA · On-site

$142K - $191K/yr

Job Summary : eClinical Solutions is transforming clinical development with elluminate ® , their Clinical Data Cloud, which helps life sciences organizations unify and analyze their data. As a ...

eClinical Solutions

Technical Project Manager

$100K - $120K/yr

eClinical Solutions helps life sciences organizations around the world accelerate clinical development initiatives with expert data services and the elluminate Clinical Data Cloud - the foundation of ...

eClinical Solutions

Product Manager

Mansfield, MA

About eClinical Solutions eClinical Solutions is transforming clinical development with elluminate ® , our Clinical Data Cloud , helping life sciences organizations unify, analyze, and unlock the ...

eClinical Solutions

Project Manager

Mansfield, MA · Remote

eClinical Solutions helps life sciences organizations around the world accelerate clinical development initiatives with expert data services and the elluminate Clinical Data Cloud - the foundation of ...

eClinical Solutions

Senior Software Engineer

$125K - $165K/yr

Job Summary : eClinical Solutions is transforming clinical development with their Clinical Data Cloud, elluminate ® . They are seeking a Senior Software Engineer to design and develop core modules ...

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All JobsEclinical Jobs

Eclinical information

See salary details

$42K

$86.6K

$128K

How much do eclinical jobs pay per year?

As of Jul 28, 2026, the average yearly pay for eclinical in the United States is $86,556.00, according to ZipRecruiter salary data. Most workers in this role earn between $68,500.00 and $108,000.00 per year, depending on experience, location, and employer.

What is the difference between Eclinical vs Clinical Data Coordinator?

AspectEclinicalClinical Data Coordinator
Required CertificationsExperience with EDC systems, possibly certifications in clinical data managementLikely similar certifications, including data management and clinical research training
Work EnvironmentTypically works with electronic data capture (EDC) systems in clinical trialsManages and verifies clinical trial data, often using EDC systems
Employer & Industry UsageUsed by clinical research organizations, pharmaceutical companies, CROsCommonly employed in clinical research settings, hospitals, and biotech firms

Both roles involve handling clinical trial data, with Eclinical focusing on electronic systems and data management platforms, while Clinical Data Coordinators primarily verify and manage trial data. They often work together within the same industry environment, making their skills and certifications closely aligned.

What are some common challenges faced by professionals working in eClinical roles, and how can they be addressed?

EClinical professionals often encounter challenges such as adapting to rapidly evolving technology, ensuring data integrity across multiple systems, and maintaining compliance with regulatory requirements. Staying updated with software platforms and industry best practices is crucial, as is effective collaboration with clinical, data management, and IT teams. Building strong communication skills and participating in ongoing training can help address these challenges and contribute to successful clinical trial outcomes.

What is eClinical and what do professionals in this field do?

eClinical refers to the use of electronic systems and software to support the planning, management, and conduct of clinical trials. Professionals in eClinical work with technologies such as electronic data capture (EDC), clinical trial management systems (CTMS), and electronic patient-reported outcomes (ePRO) to streamline data collection, improve trial efficiency, and ensure regulatory compliance. Their tasks often include implementing digital tools, training clinical staff, managing data integrity, and ensuring that all electronic processes adhere to industry standards and regulations.

What are the key skills and qualifications needed to thrive as an Eclinical Specialist, and why are they important?

To thrive as an Eclinical Specialist, you need a solid understanding of clinical research processes, data management, and regulatory compliance, often supported by a degree in life sciences or a related field. Familiarity with EDC systems (such as Medidata Rave or Oracle InForm), CTMS platforms, and GCP certification is typically required. Strong attention to detail, problem-solving abilities, and effective communication skills help ensure data integrity and smooth collaboration with study teams. These skills are crucial for maintaining high-quality clinical trial data and supporting successful study outcomes in a regulated environment.
More about Eclinical jobs
What cities are hiring for Eclinical jobs? Cities with the most Eclinical job openings:
What are the most commonly searched types of Eclinical jobs? The most popular types of Eclinical jobs are:
What states have the most Eclinical jobs? States with the most job openings for Eclinical jobs include:
What job categories do people searching Eclinical jobs look for? The top searched job categories for Eclinical jobs are:
Eclinical jobs near you
Infographic showing various Eclinical job openings in the United States as of July 2026, with employment types broken down into 75% Full Time, and 25% Part Time. Highlights an 94% In-person, and 6% Remote job distribution, with an average salary of $86,556 per year, or $41.6 per hour.

Principal eClinical Data Strategist

Almac Group

Lansdale, PA

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 5 days ago

Job description

Almac Group is currently seeking a Principal eClinical Data Strategist for our Lansdale location.
The Principal eClinical Data Strategist is a senior individual-contributor responsible for leading the definition, governance, and continuous enhancement of Almac’s Clinical Data Management (CDM) standards, policies, and data strategy across its eClinical solutions. This role focuses on establishing cohesive, inspection-ready standards and processes across the organization and guiding teams on best practices for clinical data handling to ensure compliance with global regulatory expectations.
*This is a hybrid role
Responsibilities include but are not limited to:
Clinical Data Management (CDM) Standards / Best Practices / SOPs / Templates:
  • Define, maintain, and proactively develop CDM standards, best practices, SOPs, and templates (e.g., plans for data management, transfer, review).
  • Establish clear definitions for data types (e.g., source, electronic source, created, owned), ownership/stewardship, data handling rules (security, acceptability), privacy/PII controls, and standards for data editing, cleaning, mapping, storage, and retrieval across all Almac eClinical services.
  • Ensure cohesive CDM processes across cross-functional areas.
  • Work cross-functionally to implement.
CDM Regulatory amp; Compliance Leadership:
  • Serve as Almac’s internal expert on regulatory expectations impacting electronic clinical and eCOA data (ICH E6(R3)/E8(R1), FDA PRO/eCOA guidance, 21 CFR Part 11, GDPR).
  • Translate regulatory changes and industry trends into updated and new SOPs, standards, and required documentation; provide expert support for audits, inspections, and system validation readiness.
  • Work cross-functionally to implement, educate and ensure compliance.
eCOA Standards / Best Practices Development:
  • Lead the development, maintenance, and expansion of Almac’s eCOA standards / best practices and policies, including validated instrument implementation, scoring conventions, versioning/translation control, metadata management, compliance and missing data conventions, and audit trail requirements to ensure scientifically robust, endpoint-quality eCOA data.
  • Work cross-functionally to implement.
Policies amp; Procedures for Controlled Access of High-Risk Data:
  • Create policies and procedures governing controlled access for high-risk data (e.g., PII, randomization data) during live studies (what/when/how), including DMC and safety review needs while preserving blinding integrity
  • Work cross-functionally to implement.
Best Practices / Standards for Clinical Integrations, Data Transfers, and Data Outputs (Reports, Exports)
Work cross-functionally with product management and data services to ensure consistency, traceability, operational utility, and regulatory fitness:
  • Integration and data transfer patterns across eClinical systems (IRT, eCOA, EDC, CTMS, CDMS, sponsor systems) with clear expectations for reliability, reconciliation, monitoring, and supportability.
  • Reusable data transfer suite (scheduled, event-driven, ad hoc extracts, APIs) including formats, metadata, frequencies, and error-handling rules.
  • Stakeholder-specific outputs (e.g., Clinical Supplies data, Biostatistics randomization extracts, operational oversight reports).
  • Endpoint-quality eCOA data Internal health-check exports / reports to support monitoring, quality oversight, and internal readiness.
  • CDISC SDTM/ADaM-aligned deliverables, including traceability, documentation standards, and metadata expectations
Lead CDM Process Improvement Initiatives
Drive key process improvement initiatives while facilitating cross-functional alignment:
  • Lead CDM initiatives and strategic workstreams that modernize data standards, workflows, and practices across eClinical solutions.
  • Provide expert guidance to internal teams on Almac’s CDM standards / SOPs, and support issue resolutions, escalations, challenges.
  • Champion CDM technology and tooling improvements that enhance automation, data quality, consistency, and efficiency.
  • Identify and evaluate CDM, data, and process issues; develop strategic solutions; and lead the design and rollout of optimized practices across all affected functions.
  • Establish compliance monitoring mechanisms to identify risks, deviations, or improvement opportunities—proposing and driving mitigation strategies.
  • Build strong relationships across functions as an eClinical SME to ensure cohesive execution of standards, aligned decision-making, and unified quality expectations.
Business Continuity, Vendor Ecosystem Management amp; Client Partnership
Strengthen Almac’s business continuity, client relationships, and external partnerships by ensuring alignment between Almac standards, partner capabilities, client needs, and evolving industry direction:
  • Manage relationships with external eClinical vendors / partners to ensure alignment with Almac’s data standards and integration approaches.
  • Monitor industry trends, regulatory developments, emerging technologies, and sponsor expectations to keep Almac’s CDM service offerings current / competitive.
  • Engage with clients to consult on complex CDM / eClinical data challenges, manage escalated issues, support business development opportunities, and maintain strong client partnerships.
  • Identify external risks that may impact business continuity; recommend mitigation strategies to preserve consistency, compliance, and reliability.
  • Advise internal leadership on market insights, client needs, and partner capabilities to support long-term data strategy, product evolution, and service model planning.
Qualifications:
Required Experience / Education:
  • Bachelor’s Degree in scientific or healthcare-related field
  • 7+ years of clinical data management or a similar role in pharmaceutical or clinical research industry (e.g., eClinical, pharmaceutical, biotech, or medical device industry/company).
  • Experience with various e-clinical technologies/software systems (including eCOA with validated instruments used for endpoints)
  • Demonstrated experience creating and governing SOPs, standards, templates, frameworks, and policies.
  • Experience communicating directly with clients.
Required Knowledge:
  • Deep understanding of clinical data management processes / best practices
  • Understanding of drug development process, and clinical trial design
  • Deep knowledge of global regulatory expectations related to eClinical software and data management (ICH E6/E8, EMA/FDA guidance, 21 CFR Part 11, GDPR).
  • Knowledge of industry-standard data analysis and reporting software (e.g., SAS and/or SQL).
  • Strong understanding of eClinical integrations, data flows, API/batch transfers, and downstream sponsor data needs.
  • Basic knowledge of CDISC standards and data interchange formats (e.g., SDTM, ADaM)
Preferred Experience / Education:
  • Masters in Life Sciences, Data Science, Biostatistics, Public Health, or related field
  • Experience with IRT systems
  • Experience supporting audits, inspections, and validation activities.
  • Prior experience collaborating with Product teams on enhancements or technical requirements.
What can Almac Group offer you?
  • Medical, Vision amp; Dental benefits from the 1st of the month following start date
  • 20 days PTO per year, accrued monthly following start date
  • 12 holidays per year as well as one day for Annual Diversity Day
  • Company paid Long and Short-term disability along with Life Insurance
  • 401k company contribution
  • Professional development programs/ continuous learning opportunities
Want to see our latest job opportunities? Follow us on LinkedIn
Almac is an exceptional, award winning, drug development solutions provider at the forefront of the pharmaceutical industry. We are a privately owned organization that has organically grown over 50 years now employing over 7,500 highly skilled personnel worldwide. Our US Headquarters is located at Souderton, PA with additional operations scattered around the US and Europe. ‘Partnering to Advance Human Health’ is more than just a tagline – it is our way of life.
Embracing diversity is at the heart of enhancing Almac Group’s unique culture and reflects our fundamental belief that all people deserve equality, inclusivity and the opportunity for advancement. We are committed to cultivating a welcoming, supportive, and inclusive environment for all. Together, we will build on the strength in our diversity and deliver exceptional solutions to advance human health globally.
RECRUITMENT AGENCIES PLEASE NOTE: Almac will only accept applications from agencies/business partners that have been invited to work on this role through our portal. Candidate Resumes/CV’s not submitted through our portal or directly to Hiring Managers will be considered unsolicited and no fee will be payable. Thank you for your cooperation.
Almac Group, Inc. is an Equal Opportunity Employer - Minorities/Women/Protected Veterans/Disabled - Proudly embracing diversity in all of its expressions.
EEO is the Law
EEO is the Law GINA Supplement
Almac provides reasonable accommodations to people with disabilities who need assistance completing the application process. Please email us at ADARequest@almacgroup.com to request assistance.

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