Responsibilities:

• Identify, escalate and resolve unauthorized data access, handling concerns from users
• Enforce the data protection by providing approved solutions and provide awareness
• Verify/resolve issues related to anomalous activity through escalations or exceptions
• Enable operational support in measuring the policy compliance and data protection requirements.
• Acknowledge, analyze and validate suspicious activities triggered from correlated events through Sailpoint file access solution (SIQ)
• Collaborate with Insider Risk Program partners to analyze, investigate, and escalate potential insider threats
• Perform L2/L3 analysis and validation on alerts received through SIQ and other reporting mechanisms such as email, phone calls, management directions, etc.
• Work with other security teams (Endpoint, Network, Messaging, Identity & Access Management, Legal, & HR) to manage & contain information security incidents and events to protect company IT assets, Intellectual Property, and company's reputation
• Promptly responding to all security incidents and providing thorough post-event analyses
• Follow and contribute to maintenance of information security standards, procedures and guidelines.
• Support internal and external assessments and audits and assist in configuring and implementing appropriate application security controls
• Update existing or create new information security metrics
• Review, process/approve, and follow-up with exception requests
  
  

Qualifications:

• 7 years of experience in information security
• Solid understanding of information security policies and procedures
• Knowledge of Threat hunting and incident triage
• Knowledge of data protection principles, data classification and taxonomy
• Knowledge with Identity and access governance concepts
  
  

Preferred:

• Bachelor's degree, preferably in Computer Science, Information Technology or related IT discipline; or equal experience
• Experience with Sailpoint file access manager(SIQ) and Exabeam
• Experience in design & execution of intellectual property governance & risk
• CISSP Certifications

Please apply on the Lifelancer platform at the below link for screening steps & quicker response.

https://lifelancer.com/jobs/view/66cdf059e6b6c4ee953a8912949f4456

Data Management lead

• Monitor study status (ie. enrollment, CRFs monitored/approved, etc.) on an ongoing basis
• Present deliverables to clients, gather feedback and propose solutions.
• Provide regular data status reports to the project team
• Oversee work of the Clinical Data Coordinator as required (quality, timeliness)
• Oversee vendors to ensure that timelines and deliverables meet sponsor and protocol requirements
• Is responsible for ongoing maintenance of the clinical database, including data review/cleaning during study conduct and during preparation for database lock/close.
• Conduct reconciliation between external data and data in the EDC system to ensure consistency, including reconciliation with sponsor safety databases for adverse events/SAE (Serious adverse events) data

Study setup Technical

• Develop the data management plan (DMP)
• Build a study-specific clinical database using the EDC system:
• Design the electronic case report form (eCRF)
• Build the clinical database in the chosen EDC independently or with the support of an EDC programmer (determined based on the complexity of the system and study.
• Coordinate the validation and testing (UAT) of the clinical database
• Support the study team with the development of external systems capturing clinical data (ePRO or IWRS), ensuring that any data transfer requirements between these systems and the EDC are documented and tested appropriately.

User training and support

• Develop eCRF completion guidelines and other training material
• Conducts training for site users/monitors on the clinical database
• Activate/de-activate new users in the clinical database in response to requests from the project manager and maintain records of such request
• Respond to users requiring assistance with the EDC system

Database close/lock

• Generate data listings and reports needed for data review in preparation for database close/lock
• Ensure that data management documentation is complete and up to date in the trial master file (TMF)
• Archive the clinical database and related documents

Requirements:

Education

1. B.Sc. or M.Sc, or in a related field of study

Experience

• 10 years of clinical data management experience in the pharmaceutical industry or in a CRO environment
• 5 years of experience as a lead data manager
• Extensive experience working with EDC systems (experience with Medrio and Medidata Rave preferred)

Knowledge And Skills

• Highly organized and detail-oriented
• Project planning and time management skills
• Strong verbal and written communication skills in English
• Understanding of the drug development process and of applicable regulations, including Good Clinical Practices (GCP), ICH Guidelines
• Good understanding of CDISC SDTM/CDASH standards
• Knowledge of MedDRA and WHODrug dictionaries, an asset

Please apply on the Lifelancer platform at the below link for screening steps & quicker response.
https://lifelancer.com/jobs/view/360adcb7ad6027bd6f2c36479ae2edf8

Key Accountabilities

• Contribute to site identification and feasibility activities.
• Responsible for all aspects of study site management. (e.g. Training site staff, ensure supply of study material, IMP and trial documents, recruitment updates, etc...).
• Responsible for collection and assessment of essential documents and perform reconciliation of Investigator Site File.
• Conduct pre-study visits, site initiation visits site monitoring visits and site closeout visits per SOPs/WPDs.
• Assesses IP accountability, dispensation, and compliance at the investigative sites.
• Prepare accurate and timely visit reports in accordance with the monitoring plan and/or SOPs.
• Collaborates with project functional leads as needed.
• Attends internal and external project calls as requested and per budget to proactively provide required site updates.
• Demonstrates working knowledge of applications and Systems (e.g. CTMS, eTMF, IVRS/IWRS and EDC).
• Facilitates site audits and audit finding resolutions.
• May supervise work of, or mentor, less experienced CRAs, based on Mentoring program.
• Serve as an observational visit leader.
• Provide feedback to management and cross-functional study team on any current or potential risks or problems affecting the conduct of the clinical trial.
• Feedback on any areas requiring improvement within the department and involvement in initiatives such as updating SOPs, Work instructions and Processes.
• Can be involved in other tasks as assigned by Management, CTMs and PMs.
• Escalate in timely manner any issue related to Quality or Data integrity.
  
  
  

SKILLS REQUIRED

• Bachelors degree in Nursing, Life Sciences or Medical Sciences or equivalent work experience required
• Previous experience as a Clinical Research Associate with strong demonstration of Clinical Research fundamentals
• Good experience in CTMS, eTMF IXRS and EDC systems
• Previous CRO experience
• Excellent communication skills
• Strong presentation skills
• Proficiency in written and spoken English; fluent in host country language
• Good knowledge of regional clinical research regulations and ICH-GCP
• Multiple therapeutic experience and proven ability to gain in-depth protocol knowledge
• Ability to establish/maintain good relationships with sites/colleagues/clients
• Ability to make decisions independently / Strong problem-solving skills
• Highly developed mentoring and motivational skills.

Please apply on the Lifelancer platform at the below link for screening steps & quicker response.

https://lifelancer.com/jobs/view/d1bc07f2c5f754440df328e7b9f756b1

ciMedian is looking for an Associate Director in Health Data Science.

SciMedian Private Limited offers outstanding education and training in Health Data Science for biomedical students across the globe with blended learning, cutting-edge lab training, and real-world experiences. Our courses aim to empower biomedical graduates to take on genuinely impactful careers while impacting human lives. In addition, we provide services in various domains of Health Data Sciences as well as Consultancy to the Pharmaceutical industry, hospitals, research organizations, and

related institutions.

To thrive as an Associate Director in Health Data Science you must be a prudent manager and an inspiring leader with a passion for transforming applications of Data Science in the Clinic, Academia and Pharmaceutical industry. The ideal candidate will have an entrepreneurial mindset and will be able to see the big picture in a variety of settings, from training to service.

Qualifications/Requirements:

• Post-graduate or PhD level degree in data science, statistics, bioinformatics, computational biology, Genomics, computational science, or a relevant discipline.
• Experience in large-scale data analysis preferably biological or health data
• Demonstrated experience in teaching through recorded content and live classes
• Experience in content creation for teaching purposes and interactive learning
• Demonstrated experience in mentoring and developing talent
• Experience in delivering presentations
• Demonstrated project management experience that includes responsibility for budgets, adherence to timelines, and interacting with and presenting to senior-level executives

• Experience in Statistics, Machine learning/Artificial Intelligence, and Genomics.
• Programming experience is required (Python, R).
• Execute machine learning algorithms, network analysis, and natural language processing and understand concepts related to algorithmic fairness and ethics
• Strong analytical, organizational, and record-keeping skills
• Willing to collaborate with internal and external stakeholders
• To be successful in this role you will have:
• Interest in our mission to transform the lives of students through innovative training and services
• Passion for health data analysis (e.g., integration and analysis of clinical data and other data sets (social determinants, patient-generated health data, wearables/devices, etc.)
• Ability to work with cloud computing environments and use leading-edge data science tools.
• Proven leadership skills and the ability to motivate and generate enthusiasm in individuals
• Excellent communication skills including the ability to concisely explain complicated concepts
• Experience building and leading multi-disciplinary teams

We offer:

• An attractive salary, depending on the experience and/or stock options
• Excellent atmosphere for growth and innovation
• Career Development opportunities
• Flexible work atmosphere, most operations can be home office
• Opportunities to lead an innovative startup to success
• Opportunity to work with teams and students worldwide

Lifelancer ( https://lifelancer.com ) is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech, data science and IT domains.

Please use the below Lifelancer link for job application and quicker response.

https://lifelancer.com/jobs/view/9a02a655043b3f696090ab0fcda81a86

Postdoctoral Fellows will lead their own projects, contribute to other projects on a collaborative basis (both in the lab and with external collaborators) and may guide PhD students in their research. The ability to work in a team is essential. Noteworthy is that the group of Folkert van Werven will move before the spring of 2027, and the postdoctoral fellow is expected to move with the group.

Key experience and competencies

• The post holder should embody and demonstrate our core Crick values: bold, imaginative, open, dynamic and collegial. The ideal candidate must have:
• Strong interest in and desire to do basic research in transcription/RNA biology
• Affinity with techniques in molecular biology, biochemistry, bioinformatics, genetics, and genomics
• Apart from working on the main project, a successful candidate should also be able to help others and collaborate with members of the research group

Essential

• PhD in either Molecular biology/Biochemistry/Genomics/Genetics/Computational Biology or in the final stages of PhD submission
• Track record of writing papers as evidenced by publications or submitted manuscripts in referred journals
• Evidence of data presentation at scientific meetings
• Ability to work independently as well as interacting within a group

Desirable

• Technical expertise in various molecular biology and biochemical techniques and data analyses
• Experience in using yeast as model including yeast genetics
• Experience in RNA related techniques (such as RNA-seq and CLIP-seq)
• Experience with bioinformatics and genomics

Lifelancer ( https://lifelancer.com ) is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech, data science and IT domains.

Please use the below Lifelancer link for job application and quicker response.

https://lifelancer.com/jobs/view/eb4a6141c3dcacfa52beadf218cf79f2

We are looking for an enthusiastic Post-doctoral Research Associate to join the team of Dr Nordine Helassa on a British Heart Foundation funded project.

Long QT syndrome (LQTS) is an inherited disorder associated with increased risk of life-threatening cardiac events. It affects approximately 1:2500 people and those living with LQTS experience seizure, fainting, and potentially life-threatening arrhythmias. This project uses a multi-disciplinary approach to provide new insights into the molecular mechanism of LQTS and inspire new therapeutic strategies.

You should have a PhD degree in Biochemistry, Physiology, Cell Biology or related discipline. Experience working with proteins, confocal microscopy or patch-clamp electrophysiology would be desirable.

If you are still awaiting your PhD to be awarded you will be appointed at Grade 6, spine point 30. Upon written confirmation that you have been awarded your PhD, your salary will be increased to Grade 7, spine point 31.

This is a fixed-term post available for 3 years.

The University of Liverpool is committed to enhancing workforce diversity. We actively seek to attract, develop, and retain colleagues with diverse backgrounds and perspectives. We welcome applications from all genders/gender identities, Black, Asian, or Minority Ethnic backgrounds, individuals living with a disability, and members of the LGBTQIA+ community.

Lifelancer ( https://lifelancer.com ) is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech, data science and IT domains.

Please use the below Lifelancer link for job application and quicker response.

https://lifelancer.com/jobs/view/e40a9840d1e1de16be5f53030194f572