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  • Posted: Oct 22, 2025
    Deadline: Not specified
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  • Signant Health is the evidence generation company, uniquely providing a single source for comprehensive clinical trial technology, services/support, and expertise. Trusted by researchers worldwide for more than 20 years, we transform evidence generation with industry-pioneering software solutions supported by in-house expertise in science, medicine, regulato...
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    R&D Support Engineer - Technology R&D

    Where do you fit in?

    • The R&D Support Engineer provides excellent internal customer service and resolves infrastructure and application incidents from production and pre-production environments which are escalated to R&D.

    As part of our team, your main responsibilities will be to: 

    • Investigates and resolves infrastructure and application incidents from production and pre-production environments which are escalated to R&D.
    • Collaborates with Product Management, Operations teams and R&D teams to ensure high quality support services for internal customers.
    • Assists, manages and triages incidents and service requests for R&D support.
    • Determines root cause of issues.
    • Verifies that all necessary requirements, incident details, sample data, and other supporting information is provided with each incident or service request submitted.
    • Possesses or quickly gains detailed knowledge of the company’s products to effectively document and support the products.
    • Tracks progress of R&D support tickets with a focus on meeting delivery deadlines.
    • Collaborates with R&D teams for ensuring the appropriate resources are engaged for timely action and proper traction.
    • Communicates proactively request status to internal customers.
    • Provides data and reporting R&D support tickets status as needed.

    You’ll need to bring: 

    • Bachelor’s Degree in software engineering or computer science required. Master’s Degree is a plus.
    • Minimum of four years’ experience in a software development environment.
    • Strong experience working directly with customers.
    • Basic knowledge of web services and API.
    • Understanding of SQL language.
    • Basic knowledge of scripting languages (Perl, Shell).
    • Good understanding of computer systems, mobile devices and other tech products.
    • Strong analytical and organizational skills.
    • Problem-solving attitude and motivation to achieve the company’s goals and objectives.
    • Ability to learn quickly and adapt to change.
    • Strong and collaborative work ethic, team-orientedperson with a “can do” attitude, high integrity and critical thinker.
    • Strong communication and interpersonal skills.
    • Must be ableto deal effectivelywith all levels of the organization.
    • Ability to communicate technical issues to non-technical business colleagues.
    • Passion and demonstrated ability for continuous process improvement.
    • Excellent decision making.

    go to method of application »

    Software Engineer - Technology R&D

    As part of our team, your main responsibilities will be to: 

    • Perform design, implementation and maintenance of product modules/sub-systems according to architecture, guidelines and good software engineering practice;
    • Take responsibility for product’s usability by creating user interfaces, creating use cases, and implementing prototypes and conducting usability tests;
    • Prepare technical documentation of product, creates user interface guidelines and conducts reviews;
    • Produce design documentation that complies with regulations;
    • Take responsibility for the unit testing and integration testing for the sprint coding;
    • Perform bug verification, release testing and support for assigned products; Researches problems discovered by Validation or Product Support and develops solutions to the problems;
    • Research and understands the marketing requirements for a product, including target environment, performance criteria and competitive issues;
    • Other responsibilities will be assigned as required.

    You’ll need to bring

    • M.Sc/B.Sc Degree in Computer Science, Engineering or Information Systems;
    • 3 - 5 years of software development experience;
    • Fluency in English, both written and verbal;
    • APIs: REST, GraphQL;
    • DB: RDBMS (SqlServer/Oracle / PostgreSQL and Non-RDMBS (MongoDB);
    • Monitoring: Dynatrace or similar;
    • Virtualization/Cloud: Docker, OpenShift / K8s;
    • Secrets Management (AWS Secrets Manager / Azure Keyvault / Hashicorp Vault);
    • Architecture: Microservices;
    • Specific programming knowledge (1 or more);
      1. Backend Java: Java (Spring), Java EE, JUnit (or similar but willing to code in JAVA/Kotlin);
      2. Python (AWS python Powertools a nice to have);
      3. AWS (serverless / lambda / dynamodb / SQS)
      4. Terraform / Cloud Formation;
    • Build tools: Maven APIs: REST.

    go to method of application »

    Associate Director Clinical - Science & Medicine

    As part of our team, your main responsibilities will be:

    • Support strategic initiatives for the Science and Medicine department and DHS group, contributing to the alignment of scientific activities with business objectives and corporate goals. Play a critical role in accelerating business development by collaborating closely with the Sales team to define and execute high-impact strategies that increase win rates and secure new opportunities.
    • Manage and develop junior clinical scientists, fostering a culture of scientific excellence, innovation, and professional growth.
    • Support the Director and leadership team by contributing to departmental planning, cross-functional initiatives, and key projects.
    • Contribute to thought leadership initiatives, including scientific publications, presentations, and external collaborations to enhance the company's scientific reputation.
    • Work with business development, marketing, and commercial teams to support partnerships, client engagements, and scientific communications.
    • Ensure scientific and clinical quality in project execution and interpretation, providing guidance on clinical and scientific issues and provide review of methodologies and deliverables.
    • Represent the company at selected Investigator’s meetings, scientific conferences, industry meetings, and with stakeholders, serving as a scientific expert.
    • Collaborate with cross-functional teams, including Operations, Product Development, and Regulatory Affairs, to implement clinical and scientific activities aligned with business goals.
    • Monitor scientific trends, industry developments, and competitive activities to inform departmental priorities and support the company's scientific position.
    • Support strategies to ensure compliance with regulatory requirements and industry standards while maintaining scientific integrity across projects.

    Decision making and influence:

    • Exercises sound decision-making on scientific implementation and prioritization to balance scientific quality with business objectives
    • Influences project teams by effectively communicating scientific concepts and their business implications
    • Provides reliable scientific guidance that informs departmental initiatives and project direction
    • Contributes to innovation through evaluation of relevant technologies, methodologies, and therapeutic approaches
    • Develops relationships with scientific peers, academic institutions, and industry partners to support company's scientific initiatives

    You’ll need to bring

    Essential:  

    • MD, PhD, PharmD, or equivalent advanced degree in a relevant scientific or medical field.
    • Minimum of 7+ years of experience in clinical research, pharmaceutical industry, or healthcare.
    • At least 3 years in a scientific or clinical management role.
    • Demonstrated record of scientific contributions and publications in peer-reviewed journals.
    • Solid understanding of clinical research methodologies and industry practices.
    • Developing leadership abilities with experience managing scientific professionals.
    • Strong communication and presentation skills.
    • Analytical thinking and developing business awareness.
    • Collaborative approach with strong interpersonal skills.
    • Commitment to scientific integrity and ethical standards.

    Desirable:

    • Experience in therapeutic areas aligned with company's focus (e.g., CNS, oncology, neurology, rare diseases)
    • Experience with digital health technologies, AI applications in clinical research, or innovative research methodologies
    • Experience in cross-functional project leadership
    • Background in clinical development or medical affairs
    • Understanding of regulatory requirements in clinical research

    go to method of application »

    Project Manager - eCOA - Operations - 2nd Shift

    We are currently looking for a Project Manager – eCOA to join our team. Please note: this role requires working a 2nd shift to support global project delivery.

    What You’ll Do

    • Lead and manage the planning, execution, and completion of projects, ensuring delivery within timelines, budget, and quality standards.

    • Oversee project systems, change control processes, and client deliverables.

    • Act as the primary point of contact for assigned clients, ensuring transparent, timely communication.

    • Handle escalations, manage risks, and provide regular project status reporting.

    • Collaborate cross-functionally to ensure client expectations are met and exceeded.

    • Contribute to company-wide process improvements and foster a culture of continuous improvement.

    What We’re Looking For

    • Bachelor’s degree or equivalent experience.

    • Prior Project Management experience (life sciences or CRO/pharma industry a plus).

    • Strong understanding of the software development lifecycle (SDLC).

    • Excellent organizational, time management, and communication skills.

    • Ability to manage multiple priorities while maintaining high quality standards.

    • Proficiency in MS Office Suite (Word, Excel, PowerPoint, MS Project).

    • PMP or equivalent certification is desirable.

    go to method of application »

    Associate Project Manager - Operations

    What You’ll Do

    • Oversee all phases of assigned projects, from planning through completion.
    • Manage multiple projects concurrently while meeting deadlines and maintaining quality standards.
    • Coordinate with global project management and technical delivery teams to ensure timely deliverables.
    • Develop, review, and approve study materials in compliance with quality governance procedures.
    • Prepare and deliver internal and external project status reports.
    • Foster strong client relationships through proactive communication and problem-solving.

    What We’re Looking For

    • 3–5 years of professional experience; project management experience preferred.
    • Proven ability to manage work plans, budgets, and deliverables.
    • Bachelor’s degree or equivalent experience.
    • Strong client/vendor relationship skills and excellent communication abilities.
    • Proficiency with Microsoft Office Suite.
    • Entrepreneurial mindset with a strong work ethic and attention to detail.
    • Ability to work the 2nd shift and travel occasionally for business.

    go to method of application »

    Project Manager - Advisory - Operations

    As part of our team, your main responsibilities will: 

    • The Project Manager is responsible for the planning, execution and completion of projects considering budget, timelines, resources and task management. The Project Manager will communicate in a transparent and timely manner with the assigned Signant Health clients and internal stakeholders. He/she will manage project risks and ensure timely resolution while reporting out on project status with the appropriate internal and external stakeholders.
    • The Project Manager contributes to the implementation of company-wide process improvements to ensure effective and efficient project delivery.
    • This role requires an effective leader that excels in problem-solving, able to motivate a result-oriented team, and can build trust-based relationships with Signant Health’s clients.

     You’ll need to bring

    • Bachelors’ degree or equivalent or relevant experience
    • Understanding of the software development life cycle and the specification and configuration of software products
    • Able to multi-task and work with multiple team members
    • Must have excellent time management, communication (oral and written), and organizational skills
    • Must be detail, and first-time quality delivery, orientated
    • Must have solid MS Office Suite experience – Word, Excel, MS Project, PowerPoint
    • Ability and experience of direct project activities and ensuring customer satisfaction while understanding and adhering to the study budget
    • Must be comfortable speaking in front of diversified and/or large audiences
    • Must be able to communicate and engage effectively with all levels of the organization and have excellent written and spoken English skills
    • Must have experience in a Project Management role OR equivalent
    • Must show initiative and be able to work independently as needed

    Desirable:

    • Background in Pharmaceutical, Medical education and/or CRO
    • Experience of clinical trials/pharmaceutical industry/life sciences
    • Ability to travel for business trips (overnight business trips could be expected quarterly)
    • Experience/understanding of the clinical research environment and GCP principles is preferred
    • PMP or equivalent certificate.

    Method of Application

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