This position will be an integral part of the Clinical Operations leadership team and requires a strong understanding of how study start-up and regulatory submissions are integrated with other ...
This position will be an integral part of the Clinical Operations leadership team and requires a strong understanding of how study start-up and regulatory submissions are integrated with other ...
Study Start-Up Coordinator- PhD
Cincinnati, OH · On-site +1
Job Summary Our clinical operations activities are growing rapidly, and we are currently seeking full-time, office-based Regulatory Submissions Coordinators to join our Study Start-up team. This ...
Study Start-Up Coordinator- PhD
Cincinnati, OH · On-site +1
Job Summary Our clinical operations activities are growing rapidly, and we are currently seeking full-time, office-based Regulatory Submissions Coordinators to join our Study Start-up team. This ...
Experienced Study Start-Up Coordinator
Cincinnati, OH · On-site +1
Job Summary Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Coordinators to join our Study Start-up team. This ...
Experienced Study Start-Up Coordinator
Cincinnati, OH · On-site +1
Job Summary Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Coordinators to join our Study Start-up team. This ...
Entry-Level Study Start-Up Coordinator
Cincinnati, OH · On-site +1
Job Summary Our clinical operations activities are growing rapidly, and we are currently seeking full-time, office-based Study Start-Up Coordinators to join our Regulatory Submissions team. In this ...
Entry-Level Study Start-Up Coordinator
Cincinnati, OH · On-site +1
Job Summary Our clinical operations activities are growing rapidly, and we are currently seeking full-time, office-based Study Start-Up Coordinators to join our Regulatory Submissions team. In this ...
Study Start-Up Coordinator- PharmD
Cincinnati, OH · On-site +1
Job Summary Our clinical operations activities are growing rapidly, and we are currently seeking full-time, office-based Regulatory Submissions Coordinators to join our Study Start-up team. This ...
Study Start-Up Coordinator- PharmD
Cincinnati, OH · On-site +1
Job Summary Our clinical operations activities are growing rapidly, and we are currently seeking full-time, office-based Regulatory Submissions Coordinators to join our Study Start-up team. This ...
Job Summary Our clinical operations activities are growing rapidly, and we are currently seeking full-time, office-based Project Coordinators to join our Regulatory Submissions/Study Start-Up team.
Job Summary Our clinical operations activities are growing rapidly, and we are currently seeking full-time, office-based Project Coordinators to join our Regulatory Submissions/Study Start-Up team.
Study Start-Up Coordinator (CRC Experience)
Cincinnati, OH · On-site +1
$23.25 - $31/hr
Job Summary Our clinical operations activities are growing rapidly, and we are currently seeking talent Clincial Research Coordinators to join our Study Start-up team. This position works both ...
Study Start-Up Coordinator (CRC Experience)
Cincinnati, OH · On-site +1
$23.25 - $31/hr
Job Summary Our clinical operations activities are growing rapidly, and we are currently seeking talent Clincial Research Coordinators to join our Study Start-up team. This position works both ...
Study Start-Up Project Manager
Cincinnati, OH · On-site +1
Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, Study Start-Up Project Manager to join our Site Activation and Maintenance team. This position plays ...
Study Start-Up Project Manager
Cincinnati, OH · On-site +1
Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, Study Start-Up Project Manager to join our Site Activation and Maintenance team. This position plays ...
This position works both independently and collaboratively with a team to meet common goals and plays a key role in the clinical trial management and study start-up process at Medpace. If you want to ...
This position works both independently and collaboratively with a team to meet common goals and plays a key role in the clinical trial management and study start-up process at Medpace. If you want to ...
Remote Clinical Psychologist - Ohio
Columbus, OH · On-site +1
$100K - $120K/yr
Schedule autonomy (7am-10pm - 7days a week) * Part-time/Contract roles start at just 18 hours per ... Paid, structured onboarding program - we will set you up for success no matter your level of ...
Quick apply
Remote Clinical Psychologist - Ohio
Columbus, OH · On-site +1
$100K - $120K/yr
Schedule autonomy (7am-10pm - 7days a week) * Part-time/Contract roles start at just 18 hours per ... Paid, structured onboarding program - we will set you up for success no matter your level of ...
... remote team environment and be able to establish strong, positive relationships with both internal departments, external clinical study sites and biospecimen vendors. The successful candidate ...
... remote team environment and be able to establish strong, positive relationships with both internal departments, external clinical study sites and biospecimen vendors. The successful candidate ...
Early Career Clinical Research Opportunities
Cincinnati, OH · On-site +1
$23.25 - $31/hr
Contribute to the progression of clinical trials from study start-up through close-out across a broad range of therapeutic areas * Collaborate across internal functions, sponsor companies, and ...
Early Career Clinical Research Opportunities
Cincinnati, OH · On-site +1
$23.25 - $31/hr
Contribute to the progression of clinical trials from study start-up through close-out across a broad range of therapeutic areas * Collaborate across internal functions, sponsor companies, and ...
Entry-Level Contract Specialist
Cincinnati, OH · On-site +1
This position plays a key role in the study start-up and clinical trial management processes at Medpace. The Contract Specialist will play a key role in advancing the start-up of our projects. If you ...
Entry-Level Contract Specialist
Cincinnati, OH · On-site +1
This position plays a key role in the study start-up and clinical trial management processes at Medpace. The Contract Specialist will play a key role in advancing the start-up of our projects. If you ...
Sr. Clinical Research Associate
Delaware, OH · On-site +1
Study & Site Management * Serve as CRA for assigned complex clinical studies, providing expert oversight of site selection, initiation, monitoring, and closeout activities (onsite, virtual, remote)
Sr. Clinical Research Associate
Delaware, OH · On-site +1
Study & Site Management * Serve as CRA for assigned complex clinical studies, providing expert oversight of site selection, initiation, monitoring, and closeout activities (onsite, virtual, remote)
Medical Writer / Clinical Document Author
Cleveland, OH · Remote
$50 - $80/hr
Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...
Medical Writer / Clinical Document Author
Cleveland, OH · Remote
$50 - $80/hr
Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...
Medical Writer / Clinical Document Author
Dayton, OH · Remote
$50 - $80/hr
Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...
Medical Writer / Clinical Document Author
Dayton, OH · Remote
$50 - $80/hr
Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...
Medical Writer / Clinical Document Author
Toledo, OH · Remote
$50 - $80/hr
Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...
Medical Writer / Clinical Document Author
Toledo, OH · Remote
$50 - $80/hr
Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...
Medical Writer / Clinical Document Author
Akron, OH · Remote
$50 - $80/hr
Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...
Medical Writer / Clinical Document Author
Akron, OH · Remote
$50 - $80/hr
Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...
Medical Writer / Clinical Document Author
Cincinnati, OH · Remote
$50 - $80/hr
Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...
Medical Writer / Clinical Document Author
Cincinnati, OH · Remote
$50 - $80/hr
Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...
Medical Writer / Clinical Document Author
Columbus, OH · Remote
$50 - $80/hr
Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...
Medical Writer / Clinical Document Author
Columbus, OH · Remote
$50 - $80/hr
Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...
Remote Clinical Study Start Up information
What is the difference between Remote Clinical Study Start Up vs Remote Clinical Data Coordinator?
| Aspect | Remote Clinical Study Start Up | Remote Clinical Data Coordinator |
|---|---|---|
| Primary Responsibilities | Planning, site selection, regulatory submissions, site initiation | Data entry, data validation, database management, data quality assurance |
| Required Credentials | Life sciences degree, knowledge of GCP, regulatory knowledge | Life sciences or related degree, familiarity with clinical data systems |
| Work Environment | Collaborates with sponsors, sites, regulatory bodies | Works mainly with data management teams and databases |
| Industry Usage | Involved early in trial setup phases | Involved during data collection and analysis phases |
Remote Clinical Study Start Up focuses on preparing and initiating clinical trials, including site selection and regulatory compliance. In contrast, Remote Clinical Data Coordinator manages and ensures the accuracy of clinical trial data during the study. Both roles require related credentials and work within the clinical research industry, but they operate at different stages of the trial process.
What are the most commonly searched types of Clinical Study Start Up jobs in Ohio?
The most popular types of Clinical Study Start Up jobs in Ohio are:
What are popular job titles related to Remote Clinical Study Start Up jobs in Ohio?
For Remote Clinical Study Start Up jobs in Ohio, the most frequently searched job titles are:
What job categories do people searching Remote Clinical Study Start Up jobs in Ohio look for?
The top searched job categories for Remote Clinical Study Start Up jobs in Ohio are:
- Clinical Trials
- Dermatology Clinical Research Remote
- Full Time Clinical Research Regulatory
- Clinical Trial Risk Based Monitoring
- Commission Clinical Trial Operations
- Icon Clinical Trial
- Clinical Research Coordinator Oncology
- Seasonal Clinical Study Startup
- Volunteer Clinical Studies
- Clinical Trial Recruitment Specialist
What cities in Ohio are hiring for Remote Clinical Study Start Up jobs?
Cities in Ohio with the most Remote Clinical Study Start Up job openings:
Director - Study Start-Up Project Management
Cincinnati, OH • On-site, Remote
8.6
Based on 12 frontline employees who took The Breakroom Quiz
14th of 74 rated research
Great coworkers
People enjoy working here
Good employer
Respectful managers
Good training
Full-time
Medical, Retirement, PTO
Re-posted 17 days ago
Job description
We are seeking an office-based Director of Study Start-Up to support our growing Study Start-Up/Regulatory Submissions team at Medpace! This position will be an integral part of the Clinical Operations leadership team and requires a strong understanding of how study start-up and regulatory submissions are integrated with other clinical operations functions throughout Medpace. Study Start-Up/Regulatory Submissions experience within a CRO is required.
Incentives can include: Competitive bonus program, sign-on/relocation bonus, and equity awards.
Location: Position can be office based in Cincinnati, Dallas or Denver.
Responsibilities- Contribute directly to the growth and strategic development of a large, global Study Start-Up team;
- Develop and identify continuous improvement opportunities of internal processes;
- Oversee Study Start-Up/Regulatory Submissions activities and timelines to ensure they are in accordance with Medpace standard operating procedures and study protocols;
- Provide input on new business development opportunities; and
- Develop and maintain relationships with clients.
- Bachelor's degree in Life Sciences or related field, Advanced degree is preferred;
- 8+ years as a study start-up senior leader within a CRO;
- Excellent presentation, negotiation, documentation, leadership, team-orientation, and interpersonal skills;
- Strong customer focus with ability to manage challenging priorities and remain flexible and adaptive in stressful situations;
- Excellent written and oral communication; and
- Experience managing and developing a team.
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.
Purpose-Driven Work
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- Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence
Collaborative Culture
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- 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
Continuous Growth & Development
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- Office based environment with on-site mentors
- Defined career paths with clear advancement opportunities
- Industry renowned onboarding and training programs designed to accelerate professional development
- Ongoing training and continuous learning opportunities throughout your career
- An environment that encourages employees to influence change, contribute ideas, and grow quickly
Other Employee Benefits
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- Competitive compensation programs that recognize and reward performance
- Comprehensive health, wellness, retirement, and PTO benefits
- Office based culture with occasional WFH that provides flexibility for eligible positions after training
- Company-sponsored social events and intramural sports
Cincinnati Headquarters Experience
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- A modern corporate campus designed to support collaboration and productivity
- Multiple on-site dining options in the heart of Madison Square
- Free on-site parking
- Convenient access to on-site 24-7 fitness and wellness facilities
What 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.
Employment Type: OTHERAbout Medpace
Sourced by ZipRecruiter
Medpace is a globally recognized clinicial contract research organization (CRO) based in Cincinnati, OH, in the United States. Established in 1992, it operates in the healthcare sector, providing scientifically-driven outsourcing solutions for the development of drugs and medical devices. It offers comprehensive services like full-service clinical development services, regulatory affairs management, clinical pharmacology, data management, statistical analysis, and medical writing. By applying a scientifically-driven, therapeutically-focused, and patient-centric approach, Medpace's mission is to accelerate the global development of safe and effective medical therapies.
Industry
Medical equipment and supplies manufacturing
Company size
1,001 - 5,000 Employees
Headquarters location
Cincinnati, OH, US
Year founded
1992