Allucent

Global drug development services for biotech

Clinical Research Associate

Clinical Research OperationsPosted on Nov 12

Full-timeTel Aviv-Yafo, IsraelHybrid

About the Job

Requirements

At least 2 years of experience as a Clinical Research Associate performing on-site monitoring.
Ability to mentor and train other Clinical Research Associates effectively.
In-depth knowledge of clinical trials and their critical success factors.
Ability to travel for up to 8 days on site per month, depending on project needs.
Strong therapeutic background.
Ability to manage people or project issues, identify problems, understand contributing factors, and implement and evaluate suitable resolutions.
Ability to define and meet project requirements.
Knowledge of regulatory submission and reporting requirements and guidelines.
Understanding of the drug development process.

Responsibilities

Provide project team members with administrative, logistical, and practical assistance, including tracking, collecting, distributing, and filing study documentation.
Track and supervise collection of ongoing study data for regular project status reporting.
Assist the Clinical Operations Manager with feasibility assessments for potential studies.
Set and maintain minimum quality standards for trial monitoring activities, documentation, reporting timeliness, compliance with objectives, and cooperation with project team members; ensure activities are tracked and reports are formatted for timely submission.
Monitor clinical study site activities to ensure adherence to Good Clinical Practice, International Council for Harmonisation guidelines, standard operating procedures, and study protocols.
Collect and review regulatory documents.
Prepare site visit and telephone reports.
Manage responsibilities across multiple projects, working independently and as part of a team.
Participate in study development and start-up, including reviewing protocols, drafting monitoring plans, designing or reviewing case report forms, preparing informed consent forms, developing study documents, organizing and presenting at investigator meetings, supporting monitoring strategy, and developing project-specific Clinical Research Associate training.
Resolve site issues and determine investigational product shipment status.
Work with Project Managers, Clinical Team Leaders, Lead Clinical Research Associates, regulatory team members, and sponsors to secure authorization of regulatory documents and contracts.
Translate, coordinate translations, or review completed translations of critical documents.
Participate in feasibility and site identification activities.
Assist the project team with day-to-day clinical study management.
Review, manage, resolve, and escalate Monitoring Visit Reports as required.
Train, mentor, or supervise junior staff.
Serve as a Lead Clinical Research Associate on regional or global studies when assigned.
Review essential documents as a second-line or independent reviewer when assigned.
Conduct project co-monitoring, assessment visits, and team training.
Serve as the site contact for protocol clarifications and subject enrollment when the Clinical Research Associate is unavailable.
Participate in developing study newsletter communications.
Assist with developing project-specific team training materials.
Liaise with Business Development and present to potential clients as required.
Manage preparation of local clinical trial applications for regulatory submissions for new drugs, biologics, or devices when assigned.

Clinical Research Associate (Israel)

Allucent · Tel Aviv-Yafo, Israel (Hybrid) · Full-time · Posted 2026-11-12

Workplace: hybrid

Department: Clinical Research Associate (CRA) Team

Description

At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.

We are looking for a Clinical Research Associate (CRA) to join our A-team (hybrid*/remote). As a CRA at Allucent, you will independently control and monitor investigational sites, pro-actively detect issues, provide solutions to ensure clinical studies are performed according to the trial protocol and in compliance with SOPs, applicable regulations, and the principles of Good Clinical Practice.

In this role your key tasks will include:

Provide functional assistance to the project team members with administrative, logistical and practical issues, including the tracking, collection, distribution and filing study documentation.
Track and supervise collection of ongoing study data for purpose of regular project status reporting as required.
Assist the Clinical Operations Manager in conducting feasibility assessment for potential studies.
Govern minimum quality standards for trial monitoring activities, with respect to documentation, punctuality of reporting, compliance with objectives, and co-operation with other project team members. Ensure adequate tracking is in place for all activities and reports formatted as required for submission within agreed timelines.
Monitor activities at clinical study sites to assure adherence to GCP, ICH, SOPs, and study protocols.
Collect and review regulatory documents as required.
Prepare site visit and telephone reports.
Responsible for multiple projects and must work both independently and in a team environment.
May participate in the study development and start-up process including reviewing protocols, drafting of the Monitoring Plan, designing and/or reviewing CRFs, preparing Informed Consent forms, developing study documents, organizing and presenting at investigator meetings, working with management on monitoring strategy, and/or developing project-specific CRA training.
Resolve site issues and determine status for IP shipment.
Work with Project Manager (PM), Clinical Team Leader (CTL) and/or Lead Clinical Research Associate (LCRA), regulatory team members or Sponsor to secure authorization of regulatory documents and contracts.
May translate, coordinate translations or review completed translations of critical documents.
Participate in feasibility and/or site identification activities.
Assist the Project Team with the day-to-day management of clinical studies as required.
Monitoring Visit Report (MVR) review, management, resolution and escalation as required.
Train, mentor and/or supervise junior staff.
May be assigned as LCRA to a regional or global study.
May be assigned as a reviewer of essential documents (GLP) as a 2nd line or Independent Reviewer (IR).
Conducts project co-monitoring, assessment visits and team training.
Site contact for protocol clarifications and subject enrolment if CRA unavailable.
Participate in the development of study newsletters communication as required.
Assist with the development of project-specific training materials for team.
Liaise with Business Development and make presentations to potential clients as required.
May be required to manage the preparation of local clinical trial applications (for regulatory submissions for new drugs, biologics, or devices).

Requirements

To be successful you will possess:

At least 2 years experience as CRA (on-site monitoring).
Skills to mentor and train other CRAs in a positive and effective manner.
In-depth knowledge of clinical trials and the critical elements for success in clinical trials.
Ability to travel for up to 8 days on site per month, depending on the project needs.
Strong therapeutic background.
Has shown ability to successfully manage people/project issues.
Mature management skills demonstrated by calm and thorough review of situations. Proactively identifies and addresses problems. Seeks to understand all contributing factors. Proposes, implements, and evaluates appropriate resolutions.
Demonstrates the ability to define and meet project requirements.
Can demonstrate flexibility for improvement and creating solutions.
Proven organizational abilities, and excellent written and oral communication and presentation skills.
Excellent team player with team building skills.
Strong customer focus.
A thorough knowledge of regulatory submission and reporting requirements and guidelines.
Excellent understanding of the drug development process.

Benefits

Benefits of working at Allucent include:

Comprehensive benefits package per location
Competitive salaries per location
Departmental Study/Training Budget for furthering professional development
Flexible Working hours (within reason)
Participation in our enriching Buddy Program as a new or existing employee
Internal growth opportunities and career progression
Financially rewarding internal employee referral program
Eligibility for our Spot Bonus Award Program in recognition of going above and beyond on projects
Eligibility for our Loyalty Award Program in recognition of loyalty and commitment of longstanding employees

Disclaimers:

*Our in-office work policy encourages a dynamic work environment, prescribing 2 days in office per week for employees within reasonable distance from one of our global offices.

“The Allucent Talent Acquisition team manages the recruitment and employment process for Allucent (US) LLC and its affiliates (collectively “Allucent”). Allucent does not accept unsolicited resumes from third-party recruiters or uninvited requests for collaboration on any of our open roles. Unsolicited resumes sent to Allucent employees will not obligate Allucent to the future employment of those individuals or potential remuneration to any third-party recruitment agency. Candidates should never be submitted directly to our hiring managers, employees, or human resources.”

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About the Company

Allucent

Global drug development services for biotech

Allucent provides global drug development services aimed at small and mid-sized biotech firms. Its offerings include therapeutic strategies, clinical trial operations, biometrics, and clinical pharmacology to support regulatory planning and execution. The company works by partnering with biotech teams to design and run clinical studies, extend in-house capabilities, and ensure accurate data collection and analysis across more than 60 countries. It differentiates itself by focusing on smaller biotech clients with end-to-end, globally coordinated development programs, backed by deep regulatory and scientific expertise and long-term collaborations. The goal is to help clients bring new therapies to market safely and efficiently through practical, hands-on development support.

Company size: 1,001-5,000
Company stage: Not listed
Total funding: Not listed
Headquarters: Cary, NC
Founded: 2022

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