Proj Manager, Data Management job in

This vacancy has now expired. Please see similar roles below...

Project Manager, Data Management

This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. Responsible for managing data management teams, studies and programs of studies under the general direction of Sr. Project Manager or the Director of Data Management. Work with Clinical Operations, CDMS, Biostatistics, CDS, ITG, Medical Writing, Regulatory Affairs and Quality Assurance to ensure that data collected during trials are managed according to corporate standards and meet regulatory guide lines for data integrity.

Overview of the Role

Recognize exemplify and adhere to ICON's values which centers around our commitment to People, Clients and Performance .
As a Manager, the employee is expected to recognize the importance of and create a culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs.
Travel (approximately 15%) domestic and/or international.
Manage the Data Management team, study and or program of studies to ensure project objectives are met within budget, to agreed timeline and to high level of quality.
Manage clinical data management staff as appropriate, including but not limited to resource planning. Recruitment, performance evaluations and training .
Develop and foster sponsor relationships through effective project management and communication.
Represent or offer significant contributions to the representation of data management on specific sponsor partnerships and/or alliances provide regular status reports and KPls to senior management and represent Data Management at oversight meetings.
Manage the forecast and revenue recognition process by continuous review of monthly files and incremental review of project analysis files to meet departmental objectives for profit and margins.
Represent Data Management at internal and external audits and manage findings through resolution both operationally and within the Quality Management System
Provide Project Management to Biostatistics and Medical Writing when Clinical Operations is not a function provided by ICON.
Contribute to the development, implementation and maintenance of guidelines and procedures (SOPs, Training manuals, etc.) to facilitate the efficient performance of data management activities.
Actively participate in departmental and company initiatives.
Actively participate in the development of departmental specific training courses and conduct instructor led training courses for data management staff.
Provide input into CRF design, protocol review, edit check specifications, data entry conventions, monitoring guidelines, and any other study related documents , as required.
Actively participate in Business Development presentations to sponsors as required.
Assist Business Development colleagues with the preparation of Data Management bids as required.
Provide other general duties as required to support the company.
Develop supporting staff skills, encourage growth and provide regular performance feedback in one to one meetings and interim/yearly appraisals.
Manage staff and set clear goals and objectives .
Address performance issues promptly and devise a development plan to address areas for development.
Effectively manage work priorities of self and direct reports, delegating responsibilities where appropriate .
Monitors compliance to ensure studies are in line with internal quality Initiatives and that they are inspection ready.
Monitor compliance to Track wise responses, PV timesheets, Veeva Vault; learn to ensure no backlogs built.
Acts as mentor to all junior staff levels.

Role Requirements

To perform this job successfully , an individual must be able to perform each essential duty satisfactorily . The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions .
US/LATAM/CAN : A minimum of 6 years clinical data management experience. A minimum of 3 years' experience as a data management lead or point of contact for day to day activity on studies with key responsibilities for study set-up and close-out tasks as well as overseeing and coordinating tasks delegated to the study team members.
EU/APAC: In depth proven clinical research industry experience.
Appropriate experience and understanding of at least one clinical data management system (e.g. RAVE, INFORM, OCRDC)
Knowledge of FDA regulations and all relevant local or regional regulations respecting data quality and clinical trials conduct.
Strong written and oral communication skills.
Proven leadership skills.
Capability to work within a team environment
Capability to manage competing priorities in a changeable environment. .
Capability to handle stressful situations and deadlines,
Excellent interpersonal skills.
Due to the nature of this positibn, it may be required for the employee to travel. Therefore, dependent on the employee's location, the employee may be required to possess a valid Driver's license.

Benefits of Working in ICON

Other than working with a great team of smart and energetic people, we also offer a very competitive benefits package. This varies from country to country so a dedicated recruiter will discuss this with you at interview stage.

We care about our people as they are the key to our success. We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term career.

What’s Next?

Following your application you will be contacted by one of our dedicated recruiters and if successful we will be able to provide you with more details about this opportunity.

ICON is an equal opportunity employer - M/F/D/V and committed to providing a workplace free of any discrimination or harassment.

ICON is an equal opportunity employer - Minorities/Females/Disabled/Veterans and committed to providing a workplace free of any discrimination or harassment.

Application process

Once you find a job opening that fits your skills and interests, you can create an account, apply and check back on the progress of your application or apply for other roles. Once your application has been received, a confirmation email will be sent to your email.

Remember: this is our first time meeting you. Read the job description and highlight on your CV those experiences that we should learn about.

One of our experienced recruiters will read your profile and determine if you're fit for the role and the company. We are aware of instances where fake recruitment text messages and emails that can appear to come from ICON have been received by individuals. Always delete suspicious text messages or emails. Never give out personal financial information.

Reasonable Accomodations

List #1

Day in the life

Shining a Light on Endometriosis Awareness Month

Teaser label

Inside ICON

Content type

Blogs

Publish date

04/18/2024

Summary

Endometriosis Awareness: A Vital Cause In March, ICON, through its Networking Organization for Women (NOW) employee resource group, joined the global effort to raise awareness about endometriosis

Teaser label

Endometriosis Awareness Month sheds light on this often-misunderstood condition affecting millions worldwide.

The Role of Data Management in Clinical Trials

Teaser label

Industry

Content type

Blogs

Publish date

04/18/2024

Summary

Introduction to Data Management in Clinical Trials In the field of clinical research, data management plays a crucial role in ensuring the success and accuracy of clinical trials. Clinical trials

Teaser label

This blog examines the critical role of data management in clinical trials.

Navigating the Clinical Research Supply Chain

Teaser label

Industry

Content type

Blogs

Publish date

04/12/2024

Summary

Introduction to the Clinical Research Supply Chain The clinical research supply chain plays a crucial role in the successful execution of clinical trials. It encompasses a complex network of activ

Teaser label

Discover the intricate workings of the clinical research supply chain in this comprehensive guide.

View all

Similar jobs at ICON

Local Trial Manager

Salary

Location

Taiwan

Department

Clinical Trial Management

Location

Taiwan

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Trial Management

Job Type

Permanent

Description

Job Title: Local Trial ManagerWorking location: Home based ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment drivin

Reference

2024-110017

Expiry date

01/01/0001

Author

Sandy Tang

Author

Sandy Tang

Read more Shortlist Save this role

Senior CRA

Salary

Location

Taipei

Department

Clinical Monitoring

Location

Taipei

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

Senior Clinical Research AssociateWorking Location: Taiwan Home Based ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environ

Reference

2024-110013

Expiry date

01/01/0001

Author

Sandy Tang

Author

Sandy Tang

Read more Shortlist Save this role

Clinical Research Associate

Salary

Location

Taiwan

Department

Clinical Monitoring

Location

Taiwan

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

Clinical Research AssociateWorking Location: Taiwan Home Based ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment dr

Reference

2024-110015

Expiry date

01/01/0001

Author

Sandy Tang

Author

Sandy Tang

Read more Shortlist Save this role

Drug Safety Associate

Salary

Location

Japan

Department

Regulatory, Drug Safety/ Quality Assurance & Other roles

Location

Japan

Business Area

ICON Strategic Solutions

Job Categories

Drug Safety

Job Type

Permanent

Description

・成長性の高い両社の統合により、世界で1-2位を争う規模のグローバルCRO（世界で40,500名規模、日本で1,000名規模）に拡大・補完的な統合にもとづく、クライアントポートフォリオの多様化がもたらす本格的なスケールメリットの実現・さまざまな疾患領域への深い知識をはじめとする、両社が育んできた強みを活かした幅広い／質の高いソリューションの提供・最先端のテクノロジーに、スケールメリットが加わるこ

Reference

2024-109907

Expiry date

01/01/0001

Author

Daiki Matsumoto

Author

Daiki Matsumoto

Read more Shortlist Save this role

Principal Statistical Programmer

Salary

Location

Japan

Department

Biometrics Roles

Location

Japan

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Statistics

Job Type

Permanent

Description

Reference

2024-109186

Expiry date

01/01/0001

Author

Daiki Matsumoto

Author

Daiki Matsumoto

Read more Shortlist Save this role

Patient Recruitment Associate

Salary

Location

Mexico, Mexico City

Location

Mexico City

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Study Start Up

Patient Recruitment

Job Type

Permanent

Description

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own I

Reference

JR117283

Expiry date

01/01/0001

Author

Olivia Molina

Author

Olivia Molina

Read more Shortlist Save this role

Full Service

ICON Strategic Solutions

Government and public health services

Global Business Services

Overview of Service Lines

Why icon? full service mean for you?

graduate What does full service mean for you?

Proj Manager, Data Management

About the role

This vacancy has now expired. Please see similar roles below...

ICON and you

ICON history

Career Pathways

Benefits & Rewards

DE&I

Environmental, Social & Governance

Women in IT

Application process

Who we are