Senior Research Associate Job at iconplc (Portland)

Equity Research Senior Associate

The successful candidate will join the Citi Research’s Global Research Center in...

Location

India , Mumbai

Salary:

Not provided

Citi

Expiration Date

Until further notice

Requirements

Prior equity research experience of 3-5 years
Relevant work-experience in the Retail and Consumer Internet sector
Strong financial modeling skills, including full company modelling experience
Good data management and analysis skills and a high degree of comfort with Excel
Strong interpersonal skills for dealing with overseas colleagues
Ability to work under pressure, with minimal supervision, and in a team environment
Highly detail-oriented and possess strong organizational skills
Pragmatic "self-starter" who can work both independently and as part of a team

Job Responsibility

Creation and maintenance of excel models for companies under coverage
Creation and maintenance of excel models for industry sub-sectors
Tracking of sector news and analysis of periodic statistical data
Constant collaboration / information exchange with fellow associates
Background analysis as a part of active research on a company / theme
Maintenance of research products such as Dailies, preview notes and results notes
Completion of ad hoc client requests, often to deadlines
Assistance in initiation of coverage on new stocks
Support in developing new products

Fulltime

Senior Clinical Research Associate

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

Location

Taiwan , Taipei

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

Advanced degree in a relevant field such as life sciences, nursing, or medicine
Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements
Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools
Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment
Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license

Job Responsibility

Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards
Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution
Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting
Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct
Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations

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

Research Operations Senior Associate

Working at Atlassian: Atlassians can choose where they work – whether in an offi...

Location

Australia , Sydney

Salary:

Not provided

Atlassian

Expiration Date

Until further notice

Requirements

Report to our Research Operations Manager and drive key aspects of the operational strategy for improving and scaling efficient, compliant research services for all Atlassians
Engage, onboard and collaborate with strategic support partners, third party vendors, and agencies, to ensure that Atlassians have access to best in class Research Operations tools and services
Drive the quality, efficiency and effectiveness of services provided to the organisation, through performance measurement and tracking to inform insights and actions toward service delivery improvement
Manage improvement initiatives ensuring that impact is achieved through successful delivery of objectives to timelines, budget and stakeholder expectations
Partner with internal teams such as engineering, data science, design, and product management to optimise practices for customer understanding across the business
Contribute to operations thought leadership and business-oriented research services

Job Responsibility

Drive key aspects of the operational strategy for improving and scaling efficient, compliant research services for all Atlassians
Engage, onboard and collaborate with strategic support partners, third party vendors, and agencies
Drive the quality, efficiency and effectiveness of services provided to the organisation
Manage improvement initiatives ensuring that impact is achieved through successful delivery of objectives to timelines, budget and stakeholder expectations
Partner with internal teams such as engineering, data science, design, and product management to optimise practices for customer understanding across the business
Contribute to operations thought leadership and business-oriented research services

What we offer

health coverage
paid volunteer days
wellness resources

Fulltime

Freelance Senior Clinical Research Associate

TFS HealthScience is a leading global, mid-size Contract Research Organization (...

Location

Salary:

Not provided

TFS HealthScience

Expiration Date

Until further notice

Requirements

Bachelor’s degree, preferably in life sciences or nursing, or equivalent
Minimum of 2 years of experience working as a CRA (in oncology)
Ability to work in a fast-paced environment with changing priorities
Understanding of basic medical terminology and science related to assigned drugs and therapeutic areas
Solid understanding of Good Clinical Practice (GCP) regulations and ICH guidelines
Ability to work independently and within a team/matrix organization
Excellent written and verbal communication skills
Strong organizational skills
Ability and willingness to travel

Job Responsibility

Monitor clinical trials on-site and remotely in accordance with TFS/client SOPs, FDA regulations, and GCP/ICH guidelines
Review CRFs (paper or electronic) and subject source documentation for validity and accuracy
generate queries to resolve data issues
Identify site problems or deficiencies and report them to management through trip reports, memos, and communication with the Project Manager or Lead CRA
Initiate corrective actions as directed by the supervisor
Contribute to Ethics Committee/IRB application submissions and prepare required documentation in collaboration with the CTA and as directed by the Lead CRA/Project Manager
Participate in contract handling and negotiation under direction of the Lead CRA/Project Manager
Set up the Investigator Site File (ISF) and Study Master File (SMF), or support the CTA in doing so, and distribute materials to investigational sites
Collaborate with the study team on SMF maintenance
Order, ship, and reconcile clinical investigational supplies for study sites, if applicable

What we offer

competitive compensation package
comprehensive benefits
opportunity for personal and professional growth in a rewarding environment

Parttime

Senior Clinical Research Associate

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...

Location

United States

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Excellent attention to detail
Good written and verbal communication skills
Good collaboration and interpersonal skills
Good negotiation skills
Proficient in written and spoken English language required
Fluency in local language(s) required
Ability to work in an environment of remote collaborators
Ability to look for and champion more efficient and effective methods/processes of delivering quality clinical trials
Good analytical and problem-solving skills
Demonstrates ability to prioritize and manage multiple tasks with conflicting deadlines

Job Responsibility

Contributes to the selection of potential investigators
Accountable for study start-up and regulatory maintenance (in some countries)
Trains, supports, and advises Investigators and site staff in study related matters
Confirms that site staff have completed and documented the required training appropriately
Actively participates in Local Study Team (LST) meetings
Contributes to National Investigators meetings
Initiates, monitors, and closes study sites in compliance with Client Procedural Documents
Drives performance at the sites
Proactively identifies and ensures timely resolution to study-related issues
Updates CTMS and other systems with data from study sites

What we offer

Flexible work arrangements
Career growth and development
Supportive and inclusive environment
Diverse therapeutic areas and project exposure
Advanced Technology

Senior Clinical Research Associate

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...

Location

United States

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Excellent attention to detail
Good written and verbal communication skills
Good collaboration and interpersonal skills
Good negotiation skills
Proficient in written and spoken English language required
Fluency in local language(s) required
Excellent knowledge of international guidelines ICH-GCP, basic knowledge of GMP/GDP
Good knowledge of relevant local regulations
Good medical knowledge and ability to learn relevant Client Therapeutic Areas
Basic understanding of the drug development process

Job Responsibility

Contributes to the selection of potential investigators
In some countries, as required, accountable for study start-up and regulatory maintenance
Trains, supports, and advises Investigators and site staff in study related matters, including Risk Based Quality Management (RbQM) principles
Confirms that site staff have completed and documented the required training appropriately
Actively participates in Local Study Team (LST) meetings
Contributes to National Investigators meetings, as applicable
Initiates, monitors, and closes study sites in compliance with Client Procedural Documents
Shares information on patient recruitment and study site progress
Drives performance at the sites
Proactively identifies and ensures timely resolution to study-related issues

What we offer

Patient-focused in everything we do
Supportive and inclusive environment
Career growth and development
Flexible work arrangements
Diverse therapeutic areas and project exposure
Advanced Technology

Fulltime

Audit Associate or Senior Associate

This role involves applying audit foundational knowledge, participating in audit...

Location

United States , Newton

Salary:

Not provided

Robert Half

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Accounting, or other related field, required
Master’s degree in Accounting, or other related field, preferred
Two (2) or more years of experience in audit preparation
CPA, preferred but not required

Job Responsibility

Utilizing research skills
Applying audit foundational knowledge to understand potential audit issues
Gathering client information necessary for filing
Participating in audit planning
Recognizing and communicating potential risks
Preparing audit workpapers
Working with audit software applications to complete audit
Acting as the main client contact for general questions and information
Supervising and reviewing the work of Audit Associates (for Seniors)
Providing verbal and written performance feedback to associates and interns (for Seniors)

What we offer

Medical insurance
Vision insurance
Dental insurance
Life and disability insurance
Enrollment in 401(k) plan

Fulltime

Digital research associate / assistant

RONIN International is an independent, multi-award winning market research and c...

Location

Germany , Hamburg

Salary:

Not provided

RONIN International

Expiration Date

Until further notice

Requirements

Think logically and creatively
Always open-minded and interested in exploring new solutions and new tools
Work extremely precisely and meticulously
Have excellent written communication skills
Interaction with senior participants is matter-of-fact and confident
Confident in communicating with participants in other countries and with different cultural backgrounds
Can organize your work well
Have no difficulty working under pressure or with tight schedules
Can deliver high-quality results independently
Can work on multiple projects at the same time

Job Responsibility

Gain a deep understanding of the requirements and relevant profiles of each research project
Determine the digital approaches that are most suitable for the respective research project
Use different research methods to identify suitable potential participants for different projects
Recruit suitable participants for the research project
Manage campaigns on various social media platforms
Ensure that the individual steps mesh smoothly throughout the entire life cycle of a project
Coordinate regularly with other departments and other members within the Digital Department
Maintain complete records of the work progress of each project
Regularly report the progress of the projects assigned to you to Digital Supervisors and Digital Managers
Ensure that the requirements for efficiency and effectiveness are met for every project

Fulltime

Senior Research Associate

iconplc

Location:
United States , Portland

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
January 15, 2026

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iconplc

Location:United States , Portland

Category:Research and Development

Contract Type:Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:January 15, 2026

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