As an investigator-led, patient-focused research site, we play a key role in bringing new ... Coordinate legal review and contract execution as needed. * Prepare and oversee regulatory ...
As an investigator-led, patient-focused research site, we play a key role in bringing new ... Coordinate legal review and contract execution as needed. * Prepare and oversee regulatory ...
Preclinical Principal Scientist, Research & Development
Manhattan, NY · On-site
$140 - $190/hr
... contracts and CRO audits, if necessary. * Manage budgetary requirements for all research projects to support efficacy and safety programs. * Lead the effort to publish surgical research in ...
Preclinical Principal Scientist, Research & Development
Manhattan, NY · On-site
$140 - $190/hr
... contracts and CRO audits, if necessary. * Manage budgetary requirements for all research projects to support efficacy and safety programs. * Lead the effort to publish surgical research in ...
As an investigator-led, patient-focused research site, we play a key role in bringing new ... Coordinate legal review and contract execution as needed.Prepare and oversee regulatory submissions ...
Quick apply
As an investigator-led, patient-focused research site, we play a key role in bringing new ... Coordinate legal review and contract execution as needed.Prepare and oversee regulatory submissions ...
$7M/yr
... contract research organization that assists pharmaceutical and biopharmaceutical companies in identifying and overcoming research barriers in the development of cell and gene therapies. The client ...
Quick apply
$7M/yr
... contract research organization that assists pharmaceutical and biopharmaceutical companies in identifying and overcoming research barriers in the development of cell and gene therapies. The client ...
Clinical Research Coordinator II
Pittsburgh, PA · On-site
$23.50 - $31.25/hr
... in compliance with established SOPs and study protocols. The position collaborates with Contract Research Organizations (CROs), study sponsors, and project managers while screening and reviewing ...
Clinical Research Coordinator II
Pittsburgh, PA · On-site
$23.50 - $31.25/hr
... in compliance with established SOPs and study protocols. The position collaborates with Contract Research Organizations (CROs), study sponsors, and project managers while screening and reviewing ...
Research Director - Industry Contracts, Health Programs
Chicago, IL · On-site
$120 - $180/hr
Applicants must be legally authorized to work in the United States. Illinois Tech is unable to ... The Research Director will oversee project execution, support grant and contract development and ...
Research Director - Industry Contracts, Health Programs
Chicago, IL · On-site
$120 - $180/hr
Applicants must be legally authorized to work in the United States. Illinois Tech is unable to ... The Research Director will oversee project execution, support grant and contract development and ...
$7M/yr
... contract research organization that assists pharmaceutical and biopharmaceutical companies in identifying and overcoming research barriers in the development of cell and gene therapies. The client ...
Quick apply
$7M/yr
... contract research organization that assists pharmaceutical and biopharmaceutical companies in identifying and overcoming research barriers in the development of cell and gene therapies. The client ...
Research Director, Industry Contracts & Health Programs
Chicago, IL · On-site
$120K - $180K/yr
Applicants must be legally authorized to work in the United States. Illinois Tech is unable to ... The Research Director will oversee project execution, support grant and contract development and ...
Quick apply
Research Director, Industry Contracts & Health Programs
Chicago, IL · On-site
$120K - $180K/yr
Applicants must be legally authorized to work in the United States. Illinois Tech is unable to ... The Research Director will oversee project execution, support grant and contract development and ...
As an investigator-led, patient-focused research site, we play a key role in bringing new ... Coordinate legal review and contract execution as needed. * Prepare and oversee regulatory ...
As an investigator-led, patient-focused research site, we play a key role in bringing new ... Coordinate legal review and contract execution as needed. * Prepare and oversee regulatory ...
Research Director, Industry Contracts & Health Programs
Chicago, IL · On-site
$120K - $180K/yr
Applicants must be legally authorized to work in the United States. Illinois Tech is unable to ... The Research Director will oversee project execution, support grant and contract development and ...
Research Director, Industry Contracts & Health Programs
Chicago, IL · On-site
$120K - $180K/yr
Applicants must be legally authorized to work in the United States. Illinois Tech is unable to ... The Research Director will oversee project execution, support grant and contract development and ...
Contract Analyst- El Mirage
$65K - $78K/yr
Participate in process improvements and recommend opportunities to increase efficiency. Reporting Prepare routine reports related to contract activity. Assist with contract research and documentation ...
Contract Analyst- El Mirage
$65K - $78K/yr
Participate in process improvements and recommend opportunities to increase efficiency. Reporting Prepare routine reports related to contract activity. Assist with contract research and documentation ...
Contract Analyst- El Mirage
El Mirage, AZ · On-site
$65K - $78K/yr
Participate in process improvements and recommend opportunities to increase efficiency. Reporting Prepare routine reports related to contract activity. Assist with contract research and documentation ...
Contract Analyst- El Mirage
El Mirage, AZ · On-site
$65K - $78K/yr
Participate in process improvements and recommend opportunities to increase efficiency. Reporting Prepare routine reports related to contract activity. Assist with contract research and documentation ...
Senior Scientist, Translational Research
Watertown, MA · On-site
$67 - $72/hr
Oversee external research activities, to meet timelines, deliverables, and data quality with Contract Research Organizations (CROs) or academic collaborators EXPERIENCE & QUALIFICATIONS * Ph.D. in ...
Senior Scientist, Translational Research
Watertown, MA · On-site
$67 - $72/hr
Oversee external research activities, to meet timelines, deliverables, and data quality with Contract Research Organizations (CROs) or academic collaborators EXPERIENCE & QUALIFICATIONS * Ph.D. in ...
... contracts and CRO audits, if necessary. * Manage budgetary requirements for all research projects to support efficacy and safety programs. * Lead the effort to publish surgical research in peer ...
... contracts and CRO audits, if necessary. * Manage budgetary requirements for all research projects to support efficacy and safety programs. * Lead the effort to publish surgical research in peer ...
... contracts and CRO audits, if necessary. * Manage budgetary requirements for all research projects to support efficacy and safety programs. * Lead the effort to publish surgical research in peer ...
... contracts and CRO audits, if necessary. * Manage budgetary requirements for all research projects to support efficacy and safety programs. * Lead the effort to publish surgical research in peer ...
Senior Scientist, Translational Research
Watertown, MA · On-site
$67 - $72/hr
Oversee external research activities, to meet timelines, deliverables, and data quality with Contract Research Organizations (CROs) or academic collaborators EXPERIENCE & QUALIFICATIONS * Ph.D. in ...
Senior Scientist, Translational Research
Watertown, MA · On-site
$67 - $72/hr
Oversee external research activities, to meet timelines, deliverables, and data quality with Contract Research Organizations (CROs) or academic collaborators EXPERIENCE & QUALIFICATIONS * Ph.D. in ...
Perform high quality in-depth legal, corporate and other research to support the client ... other contract researchers to effectively prioritize and execute tasks * Reliable internet ...
Perform high quality in-depth legal, corporate and other research to support the client ... other contract researchers to effectively prioritize and execute tasks * Reliable internet ...
... contracts and CRO audits, if necessary. * Manage budgetary requirements for all research projects to support efficacy and safety programs. * Lead the effort to publish surgical research in peer ...
Quick apply
... contracts and CRO audits, if necessary. * Manage budgetary requirements for all research projects to support efficacy and safety programs. * Lead the effort to publish surgical research in peer ...
Tenure-Track/Tenured: Open Rank (Assistant Professor, Associate Professor, Full Professor)
College Station, TX · On-site
$110 - $160/hr
There are ample opportunities to engage in collaborative research, conduct applied and contract research, and contribute to enhancing the research portfolio and the service mission of the College and ...
New
Tenure-Track/Tenured: Open Rank (Assistant Professor, Associate Professor, Full Professor)
College Station, TX · On-site
$110 - $160/hr
There are ample opportunities to engage in collaborative research, conduct applied and contract research, and contribute to enhancing the research portfolio and the service mission of the College and ...
New
Contract Analyst- El Mirage
El Mirage, AZ · On-site
$65K - $78K/yr
... in process improvements and recommend opportunities to increase efficiency. Reporting • Prepare routine reports related to contract activity. • Assist with contract research and documentation ...
Contract Analyst- El Mirage
El Mirage, AZ · On-site
$65K - $78K/yr
... in process improvements and recommend opportunities to increase efficiency. Reporting • Prepare routine reports related to contract activity. • Assist with contract research and documentation ...
Full-time
Medical, Dental, Vision, Retirement, PTO
Re-posted 9 days ago
Job description
Rocky Mountain Clinical Research Idaho Falls, ID
Rocky Mountain Clinical Research is seeking an experienced and highly motivated Research Business Development Manager to join our growing team in Idaho Falls, ID. This is an exciting opportunity for an experienced clinical research professional who enjoys building relationships, negotiating opportunities, and helping bring innovative medical therapies to patients.
If you're energized by strategic thinking, business development, regulatory excellence, and working with pharmaceutical companies, medical device manufacturers, and research sponsors, we'd love to hear from you.
We offer a competitive salary (depending on experience) and benefits including Medical, dental, and vision insurance, 401(k) retirement plan, and Paid time off (PTO).
About Rocky Mountain Clinical Research
Rocky Mountain Clinical Research was founded on the principle of advancing medical care for patients facing complex diseases. We conduct high-quality clinical research across a range of therapeutic areas, including diabetes, evaluating medications and medical devices to determine their safety and effectiveness compared to current standards of care.
As an investigator-led, patient-focused research site, we play a key role in bringing new treatments to market while ensuring patient safety and regulatory compliance. We are a family-oriented organization that values teamwork, integrity, and long-term employee success.
Position Summary: Clinical Research Coordinator
The Research Business Development Manager is responsible for the strategic growth of Rocky Mountain Clinical Research's clinical trial portfolio. This position serves as the primary point of contact for pharmaceutical companies, biotechnology companies, contract research organizations (CROs), and research sponsors, developing new partnerships and identifying clinical trial opportunities that align with our physicians, patients, and organizational mission.
The successful candidate will oversee all aspects of study start-up, including feasibility assessments, sponsor communications, budget and contract negotiations, regulatory submissions, and study activation. Once studies are fully approved and activated, they will transition to our Research Operations Manager for day-to-day execution.
This position is ideal for someone who enjoys combining relationship building, strategic business development, negotiation, and regulatory leadership to expand a growing clinical research enterprise.
Key Responsibilities
- Develop and maintain strong relationships with pharmaceutical companies, biotechnology firms, CROs, and research sponsors.
- Identify and pursue new clinical trial opportunities aligned with organizational goals and physician interests.
- Complete feasibility questionnaires and site qualification assessments.
- Evaluate study protocols for scientific, operational, and financial feasibility.
- Develop and negotiate study budgets and Clinical Trial Agreements.
- Coordinate legal review and contract execution as needed.
- Prepare and oversee regulatory submissions, including Institutional Review Board (IRB) applications.
- Ensure compliance with FDA regulations, ICH Good Clinical Practice (GCP), sponsor requirements, and company policies during study start-up.
- Coordinate site initiation activities and successfully activate new studies.
- Collaborate closely with physicians, executive leadership, finance, regulatory personnel, and research operations staff.
- Maintain a strong pipeline of future research opportunities while cultivating long-term sponsor relationships.
- Monitor industry trends and recommend new therapeutic areas for research growth.
Required Qualifications
- Bachelor's degree in a healthcare, scientific, business, or related field.
- Minimum five years of experience in clinical research.
- Experience working directly with pharmaceutical sponsors or CROs.
- Experience with study start-up, regulatory submissions, or sponsor management.
- Strong communication, relationship-building, and negotiation skills.
- Excellent organizational and project management abilities.
- High attention to detail with the ability to manage multiple projects simultaneously.
- Ability to work independently while collaborating effectively across departments.
Preferred Qualifications
- Certified Clinical Research Professional (CCRP), Certified Clinical Research Coordinator (CCRC), or similar certification.
- Experience negotiating clinical trial budgets and contracts.
- Knowledge of FDA regulations, ICH-GCP guidelines, and IRB processes.
- Experience with investigator-initiated or industry-sponsored clinical trials.
- Business development or strategic partnership experience within healthcare or clinical research.
- Experience with multiple therapeutic areas.
Work Schedule
- Full-time, salaried position
- Monday - Friday
- Occasional travel for investigator meetings, sponsor visits, conferences, or business development activities
Ready to Join Our Team?
This is more than a business development position-it's an opportunity to directly influence the future of healthcare in our community. As our Research Business Development Manager, you'll help bring cutting-edge therapies to patients while building lasting partnerships with some of the world's leading pharmaceutical and biotechnology companies.
Join a collaborative team that values innovation, professionalism, and meaningful work. Your efforts will directly contribute to expanding access to tomorrow's treatments for patients today.
Apply today and help lead the next phase of growth at Rocky Mountain Clinical Research.
We understand your time is valuable, so we've made our application process quick and easy. If you're an experienced clinical research professional ready to take the next step in your career, we invite you to complete our initial 3-minute, mobile-friendly application. We look forward to learning more about you!
Location: 83404