Remote Clinical Director Jobs

Manage end-to-end relationship with corporate partners utilizing EAB’s technology from initial onboarding to platform implementation, through user training, problem-solving and consulting

Maintain up-to-date knowledge of competitors in early career recruitment space

Demonstrable analytical reasoning or quantitative analytical skills

Strong written and verbal communication skills

Use partner renewal conversation to identify portfolio growth opportunities

Provide insights from partner interactions to inform future research initiatives and new product development opportunities

Oversees management and content of the organisation’s website and social media

Maintains the necessary contacts to keep abreast of emerging issues of significance to the sector and the association management profession

Experience working with political officials and senior managers

Plans and develops webinars as part of the comprehensive knowledge plan

Capable of meeting budgetary requirements and operational metrics

High level skills in leadership, stakeholder communications, strategic planning, and public relations

• Responsible for Study Management and oversight of all Study Management functions internally and at the CROs

• 2-7 years’ experience as a clinical Study, Trial or Project Manager in charge of running trials.

• Company value: (Senior Management, Culture & Values, Diversity & Inclusion)

What we look for (minimum qualifications)

• Must have recent experience working for a Pharmaceutical company, biotech or a CRO.

• Working knowledge of Good Clinical Practices, monitoring, clinical and regulatory operations

Extensive knowledge of clinical research regulatory requirements and demonstrated abilities in clinical study management processes and clinical/drug development;

Strong abilities in cross-functional team leadership, driving personal and team accountabilities, working collaboratively, critical thinking, decision-making, and influencing;

Benefits of Working in ICON:

University degree (or equivalent), preferably in medical or biological sciences or discipline associated with clinical research. Advanced degree is preferred

What you will be doing:

Management of the study budget, including Task Orders, Change Orders, invoice approval and financial reconciliation process.

Minimum of 3 years of experience in running global clinical trials with a pharmaceutical, biotechnology or clinical research organization.

Must have recent experience working for a Pharmaceutical company, biotech or a CRO.

What we look for (minimum qualifications):

Benefits of Working in ICON:

Bachelor’s Degree, or international equivalent required, Life Sciences preferred.

Demonstrated ability to lead change and to build and support management teams.

Sound working knowledge of planning concepts related to budgetary, staffing, quality and strategic initiatives.

High level communication skills, demonstrated organizational, planning and interpersonal skills.

Ability to adapt readily to rapid and changing environments.

Ability to interact professionally with various levels of personnel, both internally and externally.

· 7-10 years within the pharmaceutical industry, including managerial responsibilities.

· Excellent communication skills, written and oral in English is mandatory; and French proficiency is an asset

· Good knowledge of Microsoft Office Suite

· Knowledge of international regulations

Assessing any necessary complimentary studies for registration in the case of incremental innovative products.

Evaluating the feasibility of registering potential new indications based on ongoing studies.

Management of roughly 25-30 sites in regulatory activation per FTE

Ensure country specific regulatory and data privacy requirements are incorporated into submission documents and any other documents/systems

2 years of clinical and 2+ year of experience in a clinical site activation environment

Must have recent experience working for a Pharmaceutical company, biotech or a CRO.

What we look for (minimum qualifications):

Benefits of Working in ICON:

Management of roughly 25-30 sites in regulatory activation per FTE

Ensure country specific regulatory and data privacy requirements are incorporated into submission documents and any other documents/systems

2 years of clinical and 1+ year of experience in a clinical site activation environment

Must have recent experience working for a Pharmaceutical company, biotech or a CRO.

What we look for (minimum qualifications):

Benefits of Working in ICON:

• Responsible for Study Management and oversight of all Study Management functions internally and at the CROs

• 2-7 years’ experience as a clinical Study, Trial or Project Manager in charge of running trials.

• Company value: (Senior Management, Culture & Values, Diversity & Inclusion)

What we look for (minimum qualifications)

• Must have recent experience working for a Pharmaceutical company, biotech or a CRO.

• Working knowledge of Good Clinical Practices, monitoring, clinical and regulatory operations

Knowledge of Content Management processes and systems preferred

Nurse Practitioner, with applicable clinical Senior Care experience

Support Sales and Customer teams to ensure value-focused sales cycles and outcome-oriented customer engagement.

Up to date on Senior Care Clinical Best Practices

• Responsible for Study Management and oversight of all Study Management functions internally and at the CROs

• 2-7 years’ experience as a clinical Study, Trial or Project Manager in charge of running trials.

• Company value: (Senior Management, Culture & Values, Diversity & Inclusion)

What we look for (minimum qualifications)

• Must have recent experience working for a Pharmaceutical company, biotech or a CRO.

• Working knowledge of Good Clinical Practices, monitoring, clinical and regulatory operations

Advanced: 3 to 5+ years of trial management experience.

The efficient management of local vendors

Proactive risk management and budget forecasting

Timely review of trip reports submitted by Site Managers

A minimum of a 4-year Bachelor’s degree or relevant clinical experience is required

At least 2 years of Oncology experience required

Management of roughly 25-30 sites in regulatory activation per FTE

Ensure country specific regulatory and data privacy requirements are incorporated into submission documents and any other documents/systems

2 years of clinical and 1+ year of experience in a clinical site activation environment

Must have recent experience working for a Pharmaceutical company, biotech or a CRO.

What we look for (minimum qualifications):

Benefits of Working in ICON:

2-5 years Relevant experience in clinical research or related fields (Site-Operations, Monitoring On-site/Remote, Data Management, Hospital settings), global study experience, preferred.

Ability to use analytical tools to extracting knowledge and insight from data (data mining)

In-depth knowledge of ICH/GCP regulations FDA Guidance Documents, EU Directives

In-depth knowledge of clinical monitoring procedures

We are Built by You. Your ideas influence the way we work, and your voice matters here.

Develops Risk Analytics Monitoring Plan for assigned studies · Participate in the development of study specific analytics.

Thorough knowledge of project management processes with a solid understanding of how to craft and manage a project budge

Project Manager (PM) is responsible for the overall coordination and management of clinical trials from start up through closeout activities.

Ensure appropriate communication on project-related matters with the PM Management

Perform other duties as assigned by management

4+ years' Clinical Project Management (demonstrating expertise within Renal/Rare Renal) required within a CRO setting is preferred

Define and manage project resource needs in conjunction with functional heads and establish contingency plans for key resources

Calm and competent approach to line management

Knowledge of all aspects of the contracting process, including status of legal language, budget updates, financial terms, etc.

Bachelors degree, or equivalent experience ideally in a business, scientific or healthcare discipline

10 or more years proposal and contract development experience within a CRO or equivalent relevant experience and/or demonstrated competencies.

Previous supervisory experience is preferred.

Master knowledge of industry standards relating to proposal development, and contracts including budgeting, document language processes for creation etc.

You’re passionate about technology and education related to patient care.  Prior clinical training and education delivery experience is highly preferred.

You’ve acquired 3+ years of experience as a Registered Nurse in a hospital environment.

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