CrawlJobs Logo
Parexel Logo Parexel · IT - Administration

Junior Clinical Trial Manager

Spain · Job Posted January 09, 2026
Apply Position
Job Link Share

Job Description

At Parexel FSP people make the difference. We have a crucial mission: to prevent and cure disease by delivering important new medicines and therapies to patients in need. We achieve this important goal through the knowledge, expertise, innovation, and commitment of our employees around the world. Our employees have the opportunity to do meaningful things globally while we support them locally in environments full of challenge, collaboration, flexibility and industry-leading growth potential. Parexel FSP is recruiting for a Clinical Trial Manager based in Spain. Home based role. Dedicated to a single sponsor. You will will manage individual clinical trials and/or programs as part of the Clinical Trial Working Group. We will offer you exceptional financial rewards, training, and development. Expect exciting career challenges, but with a healthy work-life balance. We value your well-being as much as that of our patients.

Job Responsibility

  • Manage external vendors and contract research organizations
  • Prepare study documents such as the Monitoring Manual, Study Operations Manual, Source Data Verification Plan and Laboratory Manual
  • Coordinate and be responsible for the design of study materials such as CRFs, patient diaries, study participation cards and source documents
  • Assist with protocol development and study report completion
  • Manage monitoring activities (may include routine on-site clinical monitoring) at clinical study sites to assure adherence to Good Clinical Practices (GCPs), SOPs and study protocols
  • Provide guidance, direction, and management to CRAs
  • Track patient enrollment
  • qualify, initiate, monitor, perform closeout activities, and review site reports
  • and assist in coordination of data management activities
  • Coordinate study supplies
  • Negotiate contracts with vendors of clinical trial services
  • Review Informed Consent Forms, CRFs, and study related materials
  • Plan and participate in investigator meetings
  • Assist and support data query process
  • Assure regulatory compliance of investigational sites with Jazz Pharmaceuticals’ SOPs and FDA and ICH guidelines
  • Ensures trial master file is current and maintained
  • Collaborate in the management of external vendors and contract research organizations to ensure efficient execution of clinical trials

Requirements

  • Strong experience in clinical trial documentation and processes (e.g., protocols, CRFs, monitoring plans)
  • Strong experience as CRA and Lead CRA
  • Strong experience of data management and query resolution in clinical trials
  • Overall knowledge of site management and monitoring procedures
  • Good Clinical Practices (GCPs) and regulatory compliance (FDA and ICH guidelines)
  • Degree in the life sciences field preferred

What we offer

  • Exceptional financial rewards, training, and development
  • Healthy work-life balance
Parexel - All Job Offers

Looking for more opportunities?

Search for other job offers that match your skills and interests.

Suggested Tags: Frontend Developer Secretary Talent Manager Salesforce Administrator Data Analyst
Similar Jobs for

Junior Clinical Trial Manager

8 matching positions

Junior Manager Clinical Research

At Fresenius Medical Care, we are the global leader in kidney care, committed to...
Location
Location
Germany , Bad Homburg
Salary
Salary:
Not provided
freseniusmedicalcare.com Logo
FMS USA Fresenius Mgmt Services Inc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Scientists or medical professionals with experience in conducting clinical trials of drugs and medical devices
  • Knowledge and experience in planning and conducting clinical trials, regulatory requirements for clinical trials, and the further utilization of clinical data (clinical evaluation, scientific publications, presentations)
  • Experience in project management
  • Structured, goal-oriented approach to work
  • Interest in new tasks
  • Analytical skills
  • Collaborative personality
  • Ability to mediate between unclear or conflicting positions
  • Ability to handle stress
  • Confident demeanor
Job Responsibility
Job Responsibility
  • Selection of competent and appropriate clinical research organisation (CRO) and other service providers
  • Negotiation of legal and financial terms and conditions concerning agreement with CRO or other service provider for preparatory activities and performance of planned studies
  • Continuous exchange with CRO and other qualified service providers in regular meetings (“Jour-fixe”)
  • Collaboration with FMC concerning concept, planning and performance of planned studies
  • Collaboration with FMC concerning preparation and review of synopsis´ and study protocols of planned studies
  • Preparation of concept, planning and performance of meetings of the (coordinating) investigators of the ongoing studies
  • Communication with all involved (coordinating) investigators of the studies, e.g., concerning the implementation of the study in the specific countries or for review of study documents etc.
  • Training of field sales force amongst others of participating countries taking part in the planned studies
  • Provision of regular updates concerning the ongoing studies within FMC core team
  • General collaboration with other departments of Fresenius Medical Care concerning studies (e.g., compliance and legal department etc.)
What we offer
What we offer
  • Individual opportunities for self-determined career planning and professional development
  • A corporate culture in which there is enough room for innovative thinking - to find the best solution together, not the quickest one
  • A large number of committed people with a wide range of skills, talents and experience
  • The benefits of a successful global corporation with the collegial culture of a medium-sized company
Read More
Arrow Right

(Junior) Manager Clinical Research

At Fresenius Medical Care, we are the global leader in kidney care, committed to...
Location
Location
Germany , Bad Homburg
Salary
Salary:
Not provided
freseniuskidneycare.com Logo
Fresenius Kidney Care Eupora
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Scientists or medical professionals with experience in conducting clinical trials of drugs and medical devices
  • Knowledge and experience in planning and conducting clinical trials, regulatory requirements for clinical trials, and the further utilization of clinical data (clinical evaluation, scientific publications, presentations)
  • Experience in project management
  • Structured, goal-oriented approach to work
  • Interest in new tasks
  • Analytical skills
  • Collaborative personality
  • Ability to mediate between unclear or conflicting positions
  • Ability to handle stress
  • Confident demeanor
Job Responsibility
Job Responsibility
  • Selection of competent and appropriate clinical research organisation (CRO) and other service providers
  • Negotiation of legal and financial terms and conditions concerning agreement with CRO or other service provider for preparatory activities and performance of planned studies
  • Continuous exchange with CRO and other qualified service providers in regular meetings ("Jour-fixe")
  • Collaboration with FMC concerning concept, planning and performance of planned studies
  • Collaboration with FMC concerning preparation and review of synopsis´ and study protocols of planned studies
  • Preparation of concept, planning and performance of meetings of the (coordinating) investigators of the ongoing studies
  • Communication with all involved (coordinating) investigators of the studies, e.g., concerning the implementation of the study in the specific countries or for review of study documents etc.
  • Training of field sales force amongst others of participating countries taking part in the planned studies
  • Provision of regular updates concerning the ongoing studies within FMC core team
  • General collaboration with other departments of Fresenius Medical Care concerning studies (e.g., compliance and legal department etc.)
What we offer
What we offer
  • Individual opportunities for self-determined career planning and professional development
  • A corporate culture in which there is enough room for innovative thinking - to find the best solution together, not the quickest one
  • A large number of committed people with a wide range of skills, talents and experience
  • The benefits of a successful global corporation with the collegial culture of a medium-sized company
  • Fulltime
Read More
Arrow Right

GynOnc Clinical Trial Regional Medical Affairs Manager

The GynOnc Clinical Trial RMAM is responsible for the successful conduction of a...
Location
Location
Germany , Munich
Salary
Salary:
Not provided
us.gsk.com Logo
GSK
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Advanced degree in medicine, pharmacy, life sciences or related field (MD, PharmD, PhD or equivalent)
  • At least 3 years experience in medical affairs, medical science liaison, clinical research or related industry role
  • Strong clinical and scientific knowledge relevant to the therapy area for the role
  • Excellent verbal and written communication skills in German and English
  • Willingness and ability to travel regularly within the assigned region
  • Solid understanding of regulatory, ethical and compliance requirements in the pharmaceutical environment
Job Responsibility
Job Responsibility
  • Lead and coordinate medical research activities on a local level to ensure high scientific and operational quality
  • Ensures that all clinical studies are planned, executed and communicated in line with regulatory standards and company objectives
  • Manage internal and external partners to ensure quality, timelines and budget are met
  • Develop regional omnichannel engagement plans, combining face-to-face and digital outreach to meet healthcare professional needs
  • Acting as a central interface between local and global Medical Affairs stakeholders, regional medical affairs managers, clinical development and clinical research organizations to ensure cross-functional collaboration
  • Plan and run regional medical activities such as advisory boards, symposia and educational meetings
  • Contributes to the generation of high-impact and robust data in clinical trials to inform treatment decisions, support product differentiation and improve outcomes for oncology patients
  • Mentor and support development of more junior medical colleagues
What we offer
What we offer
  • Competitive base salary
  • Annual bonus based on company performance
  • Flexible working options available for most roles
  • Learning and career development
  • Access to healthcare & wellbeing programmes
  • Employee recognition programmes
  • Fulltime
Read More
Arrow Right

Manager, Clinical Operations

Manager, Clinical Operations\n\nICON plc is a world-leading healthcare intellige...
Location
Location
China , Shanghai
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree in a relevant scientific discipline or healthcare-related field
  • Extensive experience in managing clinical operations, with a solid understanding of regulatory requirements and industry standards
  • Strong leadership skills with the ability to motivate and manage teams effectively in a dynamic environment
  • Proficiency in project management tools and methodologies, with a keen focus on optimizing processes
  • Excellent communication and interpersonal skills, with a proven ability to influence stakeholders and drive successful outcomes
  • Willingness to travel as required (approximately 30%)
Job Responsibility
Job Responsibility
  • Leading the operational planning and execution of clinical trials, ensuring adherence to protocols and timelines
  • Engaging with cross-functional teams to optimize trial design and enhance operational efficiency throughout the clinical development process
  • Monitoring trial progress and performance metrics, providing insights to inform decision-making and drive continuous improvement
  • Mentoring and developing junior staff, fostering a culture of collaboration and excellence within the team
  • Building strong relationships with internal and external stakeholders to facilitate smooth communication across clinical operations
What we offer
What we offer
  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others
  • Fulltime
Read More
Arrow Right

Clinical Trial Associate 3 (CTA 3)

As a SMA II at ICON, you will support the management and monitor of clinical tri...
Location
Location
Mexico , Mexico City
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree in a relevant field such as life sciences, healthcare administration, or clinical research
  • Experience in clinical research, site management, or monitoring, with a solid understanding of clinical trial processes and GCP guidelines
  • Strong organizational and project management skills, with the ability to handle multiple priorities and deadlines
  • Excellent analytical skills and attention to detail, with a focus on maintaining high-quality standards
  • Exceptional communication and interpersonal skills, with the ability to build and maintain effective relationships with site personnel and cross-functional teams
  • Willingness to travel as required (approximately 25%)
Job Responsibility
Job Responsibility
  • Coordinating monitoring activities at clinical trial sites, ensuring adherence to study protocols and timely resolution of site-related issues
  • Assisting in the preparation and review of regulatory documents, ensuring all site activities are compliant with GCP and applicable regulations
  • Collaborating with cross-functional teams to facilitate effective communication and support for trial sites throughout the study lifecycle
  • Tracking site performance metrics, analyzing data, and providing reports to enhance site management efficiency
  • Participating in training initiatives and mentoring junior staff to support their development in clinical trial management
What we offer
What we offer
  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others
  • Fulltime
Read More
Arrow Right

Manager, Clinical Data Management

The Manager – Clinical Data Management (CDM) is a senior functional expert in Cl...
Location
Location
Italy , Milano
Salary
Salary:
Not provided
it.alfasigma.com Logo
Alfasigma
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Minimum of 7 years of experience in Clinical Data Management within pharma, biotech, CRO, or academic settings
  • Bachelor’s degree in life sciences, health informatics, pharmacy, computer science, or a related field
  • Strong understanding of clinical trial processes and data management principles
  • Experience with EDC systems (e.g., Medidata Rave, Veeva EDC)
  • Expertise in eCOA and RTSM systems
  • Familiarity with data visualization tools
  • Proficiency in statistical software (e.g., SAS)
  • Knowledge of regulatory requirements and CDISC standards
  • Strong organizational and communication skills
  • High attention to detail
Job Responsibility
Job Responsibility
  • Providing data management expertise during protocol development and amendments
  • Contributing to the selection of CROs and specialized vendors for data collection and management
  • Supporting the preparation and review of RFPs related to data management services and costs
  • Acting as the primary point of contact for CROs and vendors, ensuring high-quality deliverables within agreed timelines and budget
  • Ensuring compliance with company processes, ICH E6 guidelines, and applicable regulations
  • Collaborating on study timelines from start-up through close-out
  • Supporting the development, review, and testing of data collection tools (e.g., eCRFs, eCOA systems)
  • Contributing to the creation and maintenance of data management documentation (e.g., DMPs, Edit Check Specifications, Data Validation Plans)
  • Overseeing outsourced data management activities, including data cleaning, coding, and reconciliation
  • Maintaining oversight documentation and coordinating internal data quality reviews
What we offer
What we offer
  • Competitive salary
  • Comprehensive benefits
  • Extensive opportunities for professional growth and development
Read More
Arrow Right

Manager Clinical Operations

ICON plc is a world-leading healthcare intelligence and clinical research organi...
Location
Location
Poland , Warsaw
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Advanced degree in a relevant field such as life sciences, nursing, or a related discipline
  • Extensive experience in managing clinical operations, with a solid understanding of regulatory requirements and industry standards
  • Strong leadership skills with the ability to motivate and manage teams effectively in a dynamic environment
  • Proficiency in project management tools and methodologies, with a keen focus on optimizing processes
  • Excellent communication and interpersonal skills, with a proven ability to influence stakeholders and drive successful outcomes
Job Responsibility
Job Responsibility
  • Leading the operational planning and execution of clinical trials, ensuring adherence to protocols and timelines
  • Engaging with cross-functional teams to optimize trial design and enhance operational efficiency throughout the clinical development process
  • Monitoring trial progress and performance metrics, providing insights to inform decision-making and drive continuous improvement
  • Mentoring and developing junior staff, fostering a culture of collaboration and excellence within the team
  • Building strong relationships with internal and external stakeholders to facilitate smooth communication across clinical operations
What we offer
What we offer
  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others
Read More
Arrow Right

Manager, Clinical Operations

We are currently seeking a Manager, Clinical Operations to join our diverse and ...
Location
Location
Poland , Warsaw
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Advanced degree in a relevant field such as life sciences, nursing, or a related discipline
  • Extensive experience in managing clinical operations, with a solid understanding of regulatory requirements and industry standards
  • Strong leadership skills with the ability to motivate and manage teams effectively in a dynamic environment
  • Proficiency in project management tools and methodologies, with a keen focus on optimizing processes
  • Excellent communication and interpersonal skills, with a proven ability to influence stakeholders and drive successful outcomes
Job Responsibility
Job Responsibility
  • Leading the operational planning and execution of clinical trials, ensuring adherence to protocols and timelines
  • Engaging with cross-functional teams to optimize trial design and enhance operational efficiency throughout the clinical development process
  • Monitoring trial progress and performance metrics, providing insights to inform decision-making and drive continuous improvement
  • Mentoring and developing junior staff, fostering a culture of collaboration and excellence within the team
  • Building strong relationships with internal and external stakeholders to facilitate smooth communication across clinical operations
What we offer
What we offer
  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others
Read More
Arrow Right