ZipRecruiter

Log In

1

Clinical Research Proposal Development Jobs in Indiana

Deaconess

Research Contracts Admin

Evansville, IN · On-site

$19.14 - $26.79/hr

In this role, you will help ensure the financial and operational success of clinical research studies by supporting budget development, contract administration, financial compliance, and sponsor ...

previous page

Showing results 41-60

All JobsClinical Research Proposal Development JobsClinical Research Proposal Development Jobs in Indiana

Clinical Research Proposal Development information

What are the key skills and qualifications needed to thrive in clinical research proposal development, and why are they important?

To thrive in Clinical Research Proposal Development, you need a strong background in clinical research methodologies, scientific writing, and regulatory compliance, often supported by a degree in life sciences or a related field. Familiarity with grant management systems, budgeting software, and knowledge of IRB processes and funding agency guidelines is typically required. Excellent attention to detail, project management abilities, and strong interpersonal communication make someone stand out in this role. These skills are crucial to ensure proposals are scientifically sound, compliant, and competitive for funding in a highly regulated and collaborative research environment.

What is clinical research proposal development?

Clinical research proposal development is the process of creating detailed plans for scientific studies involving human participants. This involves defining research objectives, designing study protocols, preparing budgets, and ensuring compliance with ethical and regulatory standards. The proposal often serves as a roadmap for the research team and is submitted to funding agencies or ethical review boards for approval. Properly developed proposals increase the likelihood of funding and successful project implementation.

What are common challenges faced in clinical research proposal development, and how can I prepare to address them?

A frequent challenge in clinical research proposal development is aligning the research objectives with regulatory requirements and funding agency expectations while ensuring feasibility within timelines and available resources. Effective communication and collaboration with investigators, statisticians, and compliance officers are crucial for addressing these challenges. To prepare, familiarize yourself with funding guidelines, regulatory standards, and project management best practices, and be proactive in seeking feedback from cross-functional teams throughout the proposal drafting process.

What is the difference between Clinical Research Proposal Development vs Clinical Research Coordinator?

AspectClinical Research Proposal DevelopmentClinical Research Coordinator
Primary RoleDevelops and writes research proposals to secure funding and approvalManages and oversees the daily conduct of clinical trials at sites
Required SkillsScientific writing, regulatory knowledge, project planningPatient interaction, study coordination, data collection
Work EnvironmentResearch institutions, pharmaceutical companies, academic settingsClinical sites, hospitals, research centers
CertificationsOften requires knowledge of GCP, regulatory guidelinesOften requires GCP certification, clinical trial training

While Clinical Research Proposal Development focuses on creating detailed research proposals to obtain funding and approval, Clinical Research Coordinators handle the day-to-day management of clinical trials at research sites. Both roles require understanding of GCP and regulatory standards but differ in their primary responsibilities and work environments.

What are popular job titles related to Clinical Research Proposal Development jobs in Indiana? For Clinical Research Proposal Development jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Clinical Research Proposal Development jobs in Indiana look for? The top searched job categories for Clinical Research Proposal Development jobs in Indiana are:
What cities in Indiana are hiring for Clinical Research Proposal Development jobs? Cities in Indiana with the most Clinical Research Proposal Development job openings:
Clinical Research Proposal Development jobs near you

Senior Director, Business Development - US

Worldwide Clinical Trials

Indianapolis, IN • On-site

Full-time

Re-posted 13 days ago

Job description

Who we are

We're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

Why Worldwide

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day.Join us!

What theEarly Phase Business DevelopmentDepartment does at Worldwide

The Early Phase Business Development department is a group of highly dedicated individuals working as one to bring the best-in-class customer service to our clients. This department is committed to growing and building business longevity for phase I andIbstudies while bringing on new clients and growing relationships with current clients.

What you will do

  • Achieve individual revenue andsales objectivesthrough proactive sales and marketing ofWorldwide'sservices to assigned clients.

  • Identifynew contact leads for potential clinical, bioanalytical, and ADME business.

  • Responsible for writing basic clinical and bioanalytical proposals, communicating with clients, internal Clinical Study Managers, and Bioanalytical Study Managers and other dutiesrequiredto generate new business.

  • Provide client benefit presentations ofWorldwide'sservices to all key accounts and in pursuit of all new business opportunities.

  • Provide daily updates to the Worldwide Sales Force Automation Client Contact and Mailing Database (CRM).

  • Activelyparticipateand provide account input for proposal development,pricingand database requirements.

  • Actively engage senior management in all major business presentations, and discussions on RequestsForInformation (RFI), Master Service Agreements (MSA)and Preferred Provider Agreements (PPA).

  • Able and willing to travel throughout assigned geographical territory and nationally.

What you will bring to the role

  • Excellent interpersonal, oral, and written communication skills in English

  • Demonstrate initiative and problem-solving skills by offering solutions when obstacles areidentified

  • Strong customer focus, ability to interact professionally within a sponsor contact

  • Proficiencyin Microsoft Office, CTMS, and EDC Systems

  • Excellent organizational and time territory management skills

  • Excellent strategic planning skills

  • Excellent computer skills

  • Excellent cognitive skills

Your experience

  • BA/BS in business or life sciences

  • MS or MBA preferred

  • Four (4) to six (6) years of experience in Bioanalytical Laboratory, Central Laboratory, Phase I, IIB Clinical Research or CRO industries and at least eight (8) years prior sales experience.

At Worldwide Clinical Trials, we are committed to fostering an inclusive and equitable workplace by providing transparent compensation.
The salary range for this position is annually (For hourly paid positions, the stated salary range reflects hourly rates):


United States of America - $164,000.00 - $326,000.00


The salary range provided is intended to give candidates an understanding of potential earnings. Compensation will fall within the provided range, and it not a guarantee of exact salary. The final salary will be determined based on relevant experience, performance, education, and internal equity. In addition to base salary, we offer a competitive benefits package depending on location. We ensure pay equity and transparency and comply with all applicable labor laws. Salary information will be discussed during the interview process, and we encourage candidates to inquire about compensation at any stage.

We love knowing that someone is going to have a better life because of the work we do.

To view our other roles, check out our careers page at Discover a world of difference at Worldwide!For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.

Apply