PhD Virtual Info Session – Medpace Belgium

Job Title: PhD Virtual Info Session – Medpace Belgium Job Location: UNAVAILABLE, Belgium Job Location Type: Remote Job Contract Type: Full-time Job Seniority Level: Medpace will be hosting an Online Hiring Event targeting PhD's students in life sciences. WHEN: September 22 at 11:00 AM A first pre-screening will be done and if you're selected you will receive a MS Teams invite to follow the online event. Responsibilities Below are some examples of the positions that we will discuss during the event. Associate Clinical Trial Manager: Communicate and coordinate study activities bewteen the internal project team, Sponsor, study sites, third-party vendors, working closely with the Project Coordinators and CTMs.Provide oversight and management of study supplies.Clinical Research Associate Comprehensive training program that provides resources and knowledge to monitor sites independentlyTravel to non-local, national study sites 60-80% of the timeCommunicate with medical staff and clinical research physicians on siteRegulatory Submissions CoordinatorCommunicate with research sites (doctor's offices, universities, hospitals, etc.) to collect all essential documents required before the site begins to screen patients to participate in the clinical trial;Maintain and perform ongoing quality review of trial documents within the Trial Master File (TMF);Collect, review, organize, and assemble regulatory start-up submissions (includes submissions to Institutional Review Boards QualificationsPhD in Life SciencesFluency in English with solid presentation skills Ability to work in a fast-paced dynamic industry within an international teamWilling to work office-based in Leuven Medpace OverviewMedpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries. Why Medpace?When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration. Purpose-Driven WorkWork alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence Collaborative CultureContribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.Leadership throughout Medpace is both accessible and approachable Continuous Growth & DevelopmentOffice based environment with on-site mentorsDefined career paths with clear advancement opportunitiesIndustry renowned onboarding and training programs designed to accelerate professional developmentOngoing training and continuous learning opportunities throughout your careerAn environment that encourages employees to influence change, contribute ideas, and grow quickly Other Employee BenefitsCompetitive compensation programs that recognize and reward performanceComprehensive health, wellness, retirement, and PTO benefitsOffice based culture with occasional WFH that provides flexibility for eligible positions after trainingCompany-sponsored social events Please note benefits may vary based on country. What to Expect NextA Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.This job is curated by Lifelancer. Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech and IT domains. Please apply via Lifelancer platform to get connected to the application page and to find similar roles.

Job Title: PhD Virtual Info Session – Medpace Belgium

Job Title:

Job Location: UNAVAILABLE, Belgium

Job Location:

Job Location Type: Remote

Job Location Type:

Job Contract Type: Full-time

Job Contract Type:

Job Seniority Level:

Job Seniority Level:

Medpace will be hosting an Online Hiring Event targeting PhD's students in life sciences.

Medpace will be hosting an Online Hiring Event targeting PhD's students in life sciences.

WHEN: September 22 at 11:00 AM

WHEN: September 22 at 11:00 AMWHEN: September 22 at 11:00 AMWHEN: September 22 at 11:00 AM

A first pre-screening will be done and if you're selected you will receive a MS Teams invite to follow the online event.

A first pre-screening will be done and if you're selected you will receive a MS Teams invite to follow the online event.Responsibilities

• Below are some examples of the positions that we will discuss during the event. Associate Clinical Trial Manager: Communicate and coordinate study activities bewteen the internal project team, Sponsor, study sites, third-party vendors, working closely with the Project Coordinators and CTMs.Provide oversight and management of study supplies.Clinical Research Associate Comprehensive training program that provides resources and knowledge to monitor sites independentlyTravel to non-local, national study sites 60-80% of the timeCommunicate with medical staff and clinical research physicians on siteRegulatory Submissions CoordinatorCommunicate with research sites (doctor's offices, universities, hospitals, etc.) to collect all essential documents required before the site begins to screen patients to participate in the clinical trial;Maintain and perform ongoing quality review of trial documents within the Trial Master File (TMF);Collect, review, organize, and assemble regulatory start-up submissions (includes submissions to Institutional Review Boards

Below are some examples of the positions that we will discuss during the event.

Below are some examples of the positions that we will discuss during the event.

Associate Clinical Trial Manager:

Associate Clinical Trial Manager:Associate Clinical Trial Manager:

• Communicate and coordinate study activities bewteen the internal project team, Sponsor, study sites, third-party vendors, working closely with the Project Coordinators and CTMs.

Communicate and coordinate study activities bewteen the internal project team, Sponsor, study sites, third-party vendors, working closely with the Project Coordinators and CTMs.

• Provide oversight and management of study supplies.

Provide oversight and management of study supplies.

Clinical Research Associate

Clinical Research AssociateClinical Research Associate

• Comprehensive training program that provides resources and knowledge to monitor sites independently

Comprehensive training program that provides resources and knowledge to monitor sites independently

• Travel to non-local, national study sites 60-80% of the time

Travel to non-local, national study sites 60-80% of the time

• Communicate with medical staff and clinical research physicians on site

Communicate with medical staff and clinical research physicians on site

Regulatory Submissions Coordinator

Regulatory Submissions CoordinatorRegulatory Submissions Coordinator

• Communicate with research sites (doctor's offices, universities, hospitals, etc.) to collect all essential documents required before the site begins to screen patients to participate in the clinical trial;

Communicate with research sites (doctor's offices, universities, hospitals, etc.) to collect all essential documents required before the site begins to screen patients to participate in the clinical trial;

• Maintain and perform ongoing quality review of trial documents within the Trial Master File (TMF);

Maintain and perform ongoing quality review of trial documents within the Trial Master File (TMF);

• Collect, review, organize, and assemble regulatory start-up submissions (includes submissions to Institutional Review Boards

Collect, review, organize, and assemble regulatory start-up submissions (includes submissions to Institutional Review BoardsQualifications

• PhD in Life Sciences

PhD in Life Sciences

• Fluency in English with solid presentation skills

Fluency in English with solid presentation skills

• Ability to work in a fast-paced dynamic industry within an international team

Ability to work in a fast-paced dynamic industry within an international team

• Willing to work office-based in Leuven

Willing to work office-based in LeuvenMedpace Overview

Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.Why Medpace?

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

Purpose-Driven Work

Purpose-Driven WorkPurpose-Driven Work

• Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence
• Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture

Collaborative CultureCollaborative Culture

• Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.Leadership throughout Medpace is both accessible and approachable
• Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.

Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.

• Leadership throughout Medpace is both accessible and approachable

Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development

Continuous Growth & DevelopmentContinuous Growth & Development

• Office based environment with on-site mentorsDefined career paths with clear advancement opportunitiesIndustry renowned onboarding and training programs designed to accelerate professional developmentOngoing training and continuous learning opportunities throughout your careerAn environment that encourages employees to influence change, contribute ideas, and grow quickly
• Office based environment with on-site mentors

Office based environment with on-site mentors

• Defined career paths with clear advancement opportunities

Defined career paths with clear advancement opportunities

• Industry renowned onboarding and training programs designed to accelerate professional development

Industry renowned onboarding and training programs designed to accelerate professional development

• Ongoing training and continuous learning opportunities throughout your career

Ongoing training and continuous learning opportunities throughout your career

• An environment that encourages employees to influence change, contribute ideas, and grow quickly

An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits

Other Employee BenefitsOther Employee Benefits

• Competitive compensation programs that recognize and reward performanceComprehensive health, wellness, retirement, and PTO benefitsOffice based culture with occasional WFH that provides flexibility for eligible positions after trainingCompany-sponsored social events
• Competitive compensation programs that recognize and reward performance

Competitive compensation programs that recognize and reward performance

• Comprehensive health, wellness, retirement, and PTO benefits

Comprehensive health, wellness, retirement, and PTO benefits

• Office based culture with occasional WFH that provides flexibility for eligible positions after training

Office based culture with occasional WFH that provides flexibility for eligible positions after training

• Company-sponsored social events

Company-sponsored social events

Please note benefits may vary based on country.

Please note benefits may vary based on country.

What to Expect Next

What to Expect NextWhat to Expect Next

A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.

A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.

This job is curated by Lifelancer.

This job is curated by Lifelancer.

Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech and IT domains.

Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech and IT domains.

Please apply via Lifelancer platform to get connected to the application page and to find similar roles.

Please apply via Lifelancer platform to get connected to the application page and to find similar roles.