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Almac Jobs (NOW HIRING)

Almac Group is currently looking for a Corporate Driver for our Souderton, PA location. The responsibilities of the Corporate Driver include transporting visitors, customers, company executives and ...

Almac Group is currently seeking a Clinical Supply Manager for our Souderton, PA location. Clinical Supply Managers are responsible for the successful execution of clinical supply projects; this ...

Almac is currently seeking a Financial Accountant for the Souderton, PA location. The Financial Accountant is responsible for performing accounting functions related to financial accounting, analysis ...

Production Line Lead - 2nd shift

Audubon, PA · On-site

$19 - $26/hr

Almac Group is currently seeking a 2nd Shift Production Line Lead Operator for our Audubon, PA location. The Production Line Lead will perform assigned functions at Almac Pharma Services relevant to ...

Almac Group is currently seeking an Electrical Coordinator for our Souderton, Pa . location. The Electrical Coordinator will provide coordination for the operation, inspection, and maintenance of ...

Almac Group is currently seeking a Business Development Director West Coast Territory. The BD Director's (West Coast) role is to develop new sales and enhance customer service to existing clients ...

Almac Group is currently seeking a Director - Operations for our Audubon, PA location. The Director - Operations will provide leadership for the operational functions within the Almac Pharma Services ...

Sr. Distribution Technician 1st Shift

Souderton, PA · On-site

$17.25 - $20.50/hr

Almac Group is currently seeking a 1st Shift Sr. Distribution Technician for our Souderton, Pennsylvania location. The Sr. Distribution Technician is responsible for verifying and packing clinical ...

Almac Group is currently seeking a Maintenance Technician for our Durham, NC location. The Maintenance Technician will responsible to perform maintenance and complete repairs to all areas of the ...

Almac Group is currently seeking a Maintenance Technician for our Durham, NC location. The Maintenance Technician will responsible to perform maintenance and complete repairs to all areas of the ...

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Almac information

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How much do almac jobs pay per hour?

As of Aug 2, 2026, the average hourly pay for almac in the United States is $16.11, according to ZipRecruiter salary data. Most workers in this role earn between $14.42 and $17.31 per hour, depending on experience, location, and employer.

What is the difference between Almac vs Clinical Research Associate?

AspectAlmacClinical Research Associate
Required CredentialsBachelor's degree in life sciences, relevant certificationsBachelor's degree, often with clinical research certifications
Work EnvironmentPharmaceutical and biotech labs, research facilitiesClinical trial sites, hospitals, research organizations
Employer & IndustryPharmaceutical companies, CROs, biotech firmsPharmaceutical companies, CROs, clinical trial sites

Almac primarily focuses on pharmaceutical research and development, providing laboratory and manufacturing services. Clinical Research Associates (CRAs) oversee clinical trials, ensuring compliance and data integrity. While both roles are integral to drug development, Almac employees often work in lab settings, whereas CRAs are more involved in site monitoring and trial management.

What is Almac?

Almac is a global organization that provides a range of services to the pharmaceutical and biotech industries, including drug development, clinical trial support, manufacturing, and logistics. The company specializes in helping bring new medicines to market by offering expertise in areas such as clinical trial supply, diagnostics, and commercial manufacturing. Almac is headquartered in Northern Ireland and operates internationally, supporting clients with innovative solutions throughout the drug development lifecycle.

What are the key skills and qualifications needed to thrive at Almac, and why are they important?

To thrive at Almac, candidates generally need a strong background in life sciences, chemistry, or pharmaceuticals, often supported by a relevant degree or industry experience. Familiarity with laboratory information management systems (LIMS), GMP compliance, and analytical instrumentation is highly valued. Excellent teamwork, problem-solving abilities, and strong communication skills help individuals excel in Almac's collaborative and regulated environment. These competencies are crucial to ensure quality, innovation, and compliance in delivering services to the pharmaceutical and biotech industries.

What are some common challenges faced by employees working at Almac and how can they be effectively addressed?

Employees at Almac, a global pharmaceutical and clinical services organization, often face challenges related to managing multiple projects with tight deadlines in a highly regulated environment. Effective time management and clear communication with team members are essential to balance workload and meet quality standards. Additionally, staying updated with evolving industry regulations can be demanding, but Almac typically provides comprehensive training and support to help staff remain compliant. Collaborating closely within cross-functional teams also helps address issues quickly and maintain project momentum.
What cities are hiring for Almac jobs? Cities with the most Almac job openings:
What states have the most Almac jobs? States with the most job openings for Almac jobs include:
Infographic showing various Almac job openings in the United States as of July 2026, with employment types broken down into 83% Full Time, and 17% Nights. Highlights an 94% Physical, 4% Hybrid, and 2% Remote job distribution, with an average salary of $33,506 per year, or $16.1 per hour.

Principal eClinical Data Strategist

Almac Group

Lansdale, PA

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 10 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
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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.