Clinical Trial Liaison Job at iconplc (Phoenix)

Clinical Trial Liaison

ICON plc is a world-leading healthcare intelligence and clinical research organi...

Location

Bulgaria , Sofia

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

A doctoral degree, M.D., PharmD or PhD is required
Experience in a clinical research environment in Pharma, Biotech, or CRO in scientific and/or clinical operations is preferred
Broad scientific and medical knowledge with an understanding of clinical development
Excellent interpersonal skills with the ability to develop relations with internal and external stakeholders
Proactive and self-motivated with the demonstrated ability to work collaboratively and independently
A scientific and clinical network and networking skills
Demonstrated success in persuasion, influence, and negotiation
Ability to discuss and apply technical/scientific/clinical knowledge
Strong communication and presentation skills in local (medical) language(s)
Knowledge of local healthcare landscape

Job Responsibility

Support clinical trials by providing scientific and clinical support to investigators and site staff to ensure study sites have a thorough understanding of the study design and procedures so that clinical trial goals are achieved
Function as a recruitment specialist in developing and optimising strategies at site and study level to drive successful patient enrolment
Engage on site and at industry meetings / conferences, driving strategies to widen access for patients and executing them
Collaborate cross-functionally with key stakeholders including medical & scientific leaders, advocates, and key decision makers across the ecosystem translating best practices to local tactical action

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
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others

Fulltime

Clinical Trial Liaison

As a Clinical Trial Liaison at ICON, you will design and analyze clinical trials...

Location

United States , North Carolina

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

Bachelor's degree in a relevant field, such as life sciences or healthcare
Proven experience in clinical trial enrollment or related roles
Strong analytical and problem-solving skills with the ability to interpret complex medical data
Excellent communication and interpersonal skills to build and maintain effective relationships with stakeholders
Detail-oriented with a commitment to ensuring accuracy and compliance in all aspects of clinical trial enrollment
Broad immunology experience, specific preference for dermatology, respiratory and/or allergy experience

Job Responsibility

Collaborate with cross-functional teams to design and implement effective clinical trial enrollment strategies
Analyze and interpret clinical trial data, ensuring accuracy and compliance with regulatory standards
Foster strong relationships with study sites and investigators to enhance patient recruitment and retention
Act as a liaison between sponsors, investigators, and study participants, providing support and guidance throughout the enrollment process
Contribute to the continuous improvement of enrollment processes and strategies to optimize trial outcomes

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

Clinical Trial Liaison

As a Clinical Trial Liaison at ICON, you will design and analyse clinical trials...

Location

United States , Raleigh

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

Bachelor's degree in a relevant field, such as life sciences or healthcare
Oncology experience is required
Proven experience in clinical trial enrollment or related roles
Strong analytical and problem-solving skills with the ability to interpret complex medical data
Excellent communication and interpersonal skills to build and maintain effective relationships with stakeholders
Detail-oriented with a commitment to ensuring accuracy and compliance in all aspects of clinical trial enrollment

Job Responsibility

Collaborate with cross-functional teams to design and implement effective clinical trial enrollment strategies
Analyze and interpret clinical trial data, ensuring accuracy and compliance with regulatory standards
Foster strong relationships with study sites and investigators to enhance patient recruitment and retention
Act as a liaison between sponsors, investigators, and study participants, providing support and guidance throughout the enrollment process
Contribute to the continuous improvement of enrollment processes and strategies to optimize trial outcomes

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

Clinical Trial Manager/ Sr Clinical Trial Manager (PM/ Sr PM)

Clinical Operations Lead - Early Development Oncology. ICON plc is a world-leadi...

Location

United States , Raleigh, Blue Bell

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

BS/BA degree or a relevant degree with strong emphasis on science, or equivalent experience
Minimum of five years of relevant experience in the biopharmaceutical industry or other relevant clinical research experience, with a focus on skills and competencies
Must have working knowledge of ICH Good Clinical Practices and other relevant regulatory/health
Prior experience in assisting the conduct and management of multinational clinical trials is preferred
Ability to effectively manage multiple priorities across several protocols and therapeutic areas simultaneously
Experience in oncology studies required (phase I preferred)

Job Responsibility

Participate as a member of a working group and perform special projects, as assigned, to improve the efficiency, effective and quality of the functioning of the Development Operations department
Act as preliminary liaison for study sites to convey study information, answer questions and in accordance with the escalation pathway
Develop relationships with investigational sites, HCPs, and institutions to enhance conduct of the trial
Monitor study-specific timelines and key deliverables
focus on management of all relevant external vendors (e.g., Monitoring, Sample management, IVRS, Laboratory, etc)
Participate as a member of the multi-disciplinary trial(s) team
Participate in coordinating efforts with internal Pharmacovigilance, and safety group as needed
Participate in data review and discrepancy resolution as needed
Assist in the development of the IP and co-medication strategy (quantities, labels, depots, tracking, etc.) working closely with other departments
Plan and organize meetings with team support (e.g., investigator/coordinator meetings, DMC, SMC, safety call, etc.) as appropriate

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

GynOnc Clinical Trial Regional Medical Affairs Manager

The GynOnc Clinical Trial RMAM is responsible for the successful conduction of a...

Location

Germany , Munich

Salary:

Not provided

GSK

Expiration Date

Until further notice

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

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

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

Clinical Trial Financial Analyst

Responsible for the coordination and creation of a coverage analyses for all cli...

Location

United States , Southlake

Salary:

Not provided

The University of Kansas Health System

Expiration Date

Until further notice

Requirements

High School Graduate
3 or more years of experience in Clinical Research Billing and/or Billing Compliance
2 or more years of experience in Budgeting and Medicare Coverage Analysis Development
A demonstrated understanding of Research Billing Compliance including National Coverage Determination for coverage of routine costs and the CMS Clinical Research Policy
A demonstrated knowledge of regulatory, financial and administrative requirements of Medicare and third party billing of clinical trials
Proficient in Excel, Word, PowerPoint
Proficiency in Medical Terminology

Job Responsibility

Creates coverage analysis grids and analyzes the performance of the actual coverage analysis, using CMS regulations, FDA guidance, Good Clinical Practice guidelines, and ethical policies when performing coverage analyses
Researches and applies policies, guidance, and guidelines from various sources including federal and state regulatory agencies and The University of Kansas Hospital policies
Responsible for the dissemination of relevant documents and information to various parties
Performs basic and complex billing and budget analysis in accordance with CMS regulations for all clinical trials performed at The University of Kansas Hospital and affiliates
Serves as liaison to the budget & financial analysts at the KUMC Research Institute and the KU Cancer Center Clinical Trials Office, collaborating closely to ensure that the clinical trial budget, coverage analysis, and billing matrix are all consistent and appropriate
Develops billing matrices and coverage analyses including reviewing each potentially billable item within the clinical trial and citing specific resources for the justification of appropriate designations
Applies the appropriate CDM and CPT code for potentially-billable items in the coverage analysis in order to assist Patient Financial Services in the management of claims review, as well as identifying items that are to be billed to the study sponsor by the KUMC Research Institute
Assists as needed with claims review in distinguishing research charges billed to the study versus those that may be billed to insurance payors
Must be able to perform the professional, clinical and or technical competencies of the assigned unit or department

Fulltime

Clinical Science Liaison

The Clinical Science Liaison functions as a member of the Exact Sciences Precisi...

Location

United States

Salary:

150000.00 - 230000.00 USD / Year

Exact Sciences

Expiration Date

Until further notice

Requirements

Master’s degree in a relevant health professions/sciences or related field (e.g., biotechnology, biology, health sciences, or clinical sciences leading to necessary skills) OR Bachelor’s degree in a relevant health professions/sciences or related field and 4+ years of field-based medical affairs experience in lieu of master’s degree.
5+ years of industry experience in healthcare or medical technology fields with Medical Affairs or similar industry experience.
Ability to meet any requirements set by healthcare facilities for access to those facilities (e.g. vaccination requirements, mask requirements, etc.).
Possession of a valid driver's license
no suspended, revoked, surrendered, invalid, etc. allowed.
No more than two moving violations, events, or accidents within the last 36 months.
No alcohol or drug event in which a vehicle was driven by the candidate or employee, including but not limited to Blood Alcohol Content (BAC) failure, refusal to submit to alcohol or drug test, alcohol-related suspension, etc. in the last 36 months.
No other results from the Motor Vehicle Report (MVR) check that expose Exact Sciences to what Exact Sciences deems to be an unacceptable level of liability.
Applicants must be currently authorized to work in country where work will be performed on a full or part-time basis. We are unable to sponsor or take over sponsorship of employment visas at this time.
Demonstrated ability to perform the essential duties of the position with or without accommodation.

Job Responsibility

Work cross functionally with field sales team and medical science liaison team to educate providers at cancer centers on the Exact Sciences Precision Oncology portfolio
Generate deep insight into cancer centers providers (HCPs) aligned with each.
Analyze the treatment journey in order to identify opportunities to work with HCPs to improve clinical decision making and deliver better patient oncology outcomes through the PO product portfolio.
Build a network of relationships with Key Opinion Leaders (KOLs), HCPs, other clinicians and key stakeholders across the healthcare market in order to gather insight about their dynamic needs, clinical and operational challenges and concerns that Exact Sciences can address and based on insights about the connections across clinical stakeholders across the treatment journey.
Synthesize data from a range of formal and informal sources to understand the evolving and dynamic local care system, identify opportunities to improve efficiency and effectiveness and share with sales, marketing and other cross-functional colleagues.
Demonstrate ability to understand major data sources (clinical trials, studies, published reports, etc.) relative to the use of Exact Sciences’ products, including clinical and select health economics and outcomes research data (HEOR).
Support health systems, population health leaders, and medical quality professionals by educating on clinical, public health, medical quality, and other scientific information to help guide medical decisions for patients and populations regarding Exact Sciences’ screening products and related disease states.
Prepare and deliver clinical and scientific presentations to healthcare providers, health systems and medical group leadership, and community/advocacy groups.
Work compliantly with cross-functional business partners in the field, including health system leadership and field sales teams to develop and execute scientific engagement tactics that align to brand strategy.
Collaborate cross-functionally with Exact Sciences’ internal teams to develop relevant content for scientific engagement for marketed and pipeline screening products.

What we offer

Paid time off (including days for vacation, holidays, volunteering, and personal time)
Paid leave for parents and caregivers
A retirement savings plan
Wellness support
Health benefits including medical, prescription drug, dental, and vision coverage.

Fulltime

New

Director, Research Services, Oncology

As a Director, Research Services at ICON, you will be responsible for working wi...

Location

United States , Blue Bell

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

Degree in a scientific/life sciences field
Pharm.D. or Ph.D. preferred
Minimum of 8 years of experience in oncology research or related field
Demonstrated experience leading clinical development programs in oncology (preferably late-stage)
Experience with global regulatory interactions and submissions (FDA, EMA, or other agencies)
Strong understanding of oncology clinical endpoints, trial design, and statistical considerations
Proven ability to work effectively in a cross-functional matrix environment and influence without direct authority
Track record of scientific publications and/or conference presentations
Excellent written and oral communication skills
Strong analytical and scientific writing skills

Job Responsibility

Development of protocols for clinical studies
Preparation of clinical development plans
Drafting of clinical scientific documents such as IND, IND amendments, Investigator’s Brochures, Annual Reports and other FDA submissions
Monitor, perform data review, and summarize safety and efficacy data in ongoing studies
Assist with study design for exploratory development
Lead the clinical matrix teams for assigned compounds
Represent exploratory development on project teams
Develop relationships with appropriate consultants
Write abstracts and present data at scientific meetings, both internally and externally
Serve as liaison to project teams, CROs and others

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

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Clinical Trial Liaison

Job Description

Job Responsibility

Requirements

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