... study specific vendors), equpment. Review and approve third party invoices and ensure adherence to contractual terms. Interface with the finance office in the Office of Research to ensure that ...
... study specific vendors), equpment. Review and approve third party invoices and ensure adherence to contractual terms. Interface with the finance office in the Office of Research to ensure that ...
Director, Alliance Management
Boston, MA · On-site
$180K - $252K/yr
Proactively supervise contractual obligations and outcomes for both Halozyme and its alliance ... Minimum of Bachelor's degree in business, life science or related field of study with at least 10 ...
Director, Alliance Management
Boston, MA · On-site
$180K - $252K/yr
Proactively supervise contractual obligations and outcomes for both Halozyme and its alliance ... Minimum of Bachelor's degree in business, life science or related field of study with at least 10 ...
... contractual obligations. The Site Medical Director manages primary and consultative services ... Provides treatment and orders studies, tests and ancillary services required consistent with the ...
... contractual obligations. The Site Medical Director manages primary and consultative services ... Provides treatment and orders studies, tests and ancillary services required consistent with the ...
... contractual obligations. The Site Medical Director manages primary and consultative services ... Provides treatment and orders studies, tests and ancillary services required consistent with the ...
... contractual obligations. The Site Medical Director manages primary and consultative services ... Provides treatment and orders studies, tests and ancillary services required consistent with the ...
... contractual obligations. The Site Medical Director manages primary and consultative services ... Provides treatment and orders studies, tests and ancillary services required consistent with the ...
... contractual obligations. The Site Medical Director manages primary and consultative services ... Provides treatment and orders studies, tests and ancillary services required consistent with the ...
Medical Director
$140 - $145/hr
... contractual obligations. The Site Medical Director manages primary and consultative services ... Provides treatment and orders studies, tests and ancillary services required consistent with the ...
Medical Director
$140 - $145/hr
... contractual obligations. The Site Medical Director manages primary and consultative services ... Provides treatment and orders studies, tests and ancillary services required consistent with the ...
Director, Alliance Management
$180K - $252K/yr
Proactively supervise contractual obligations and outcomes for both Halozyme and its alliance ... Minimum of Bachelor's degree in business, life science or related field of study with at least 10 ...
Director, Alliance Management
$180K - $252K/yr
Proactively supervise contractual obligations and outcomes for both Halozyme and its alliance ... Minimum of Bachelor's degree in business, life science or related field of study with at least 10 ...
Medical Director
$120 - $121/hr
... contractual obligations. The Site Medical Director manages primary and consultative services ... Provides treatment and orders studies, tests and ancillary services required consistent with the ...
Medical Director
$120 - $121/hr
... contractual obligations. The Site Medical Director manages primary and consultative services ... Provides treatment and orders studies, tests and ancillary services required consistent with the ...
Director, Alliance Management
Boston, MA · On-site
$180K - $252K/yr
Proactively supervise contractual obligations and outcomes for both Halozyme and its alliance ... Minimum of Bachelor's degree in business, life science or related field of study with at least 10 ...
Quick apply
Director, Alliance Management
Boston, MA · On-site
$180K - $252K/yr
Proactively supervise contractual obligations and outcomes for both Halozyme and its alliance ... Minimum of Bachelor's degree in business, life science or related field of study with at least 10 ...
Develop and manage comprehensive program project plans, including but not limited to, study ... contractual agreements, timelines and quality standards * Ensure compliance with regulatory ...
Develop and manage comprehensive program project plans, including but not limited to, study ... contractual agreements, timelines and quality standards * Ensure compliance with regulatory ...
Develop and manage comprehensive program project plans, including but not limited to, study ... contractual agreements, timelines and quality standards * Ensure compliance with regulatory ...
Develop and manage comprehensive program project plans, including but not limited to, study ... contractual agreements, timelines and quality standards * Ensure compliance with regulatory ...
Partner with Research Administration, to ensure compliance with ethical standards, contractual and ... Coordinate the efforts of clinician researchers to ensure appropriate patient selection, study ...
Partner with Research Administration, to ensure compliance with ethical standards, contractual and ... Coordinate the efforts of clinician researchers to ensure appropriate patient selection, study ...
Director of Pediatric Research
Danville, PA · On-site
Partner with Research Administration, to ensure compliance with ethical standards, contractual and ... Coordinate the efforts of clinician researchers to ensure appropriate patient selection, study ...
Director of Pediatric Research
Danville, PA · On-site
Partner with Research Administration, to ensure compliance with ethical standards, contractual and ... Coordinate the efforts of clinician researchers to ensure appropriate patient selection, study ...
Oversee multisite clinical trial research management operations including financial and contractual ... Serve as an operational resource for investigators, study teams, sponsors, and CROs. * Ensure ...
Oversee multisite clinical trial research management operations including financial and contractual ... Serve as an operational resource for investigators, study teams, sponsors, and CROs. * Ensure ...
Familiar with DFAR contractual terms including 252.225-7039/7040, providing oversight and ... of study Preferred three plus (5+) years of Security Management experience Experience with ...
Familiar with DFAR contractual terms including 252.225-7039/7040, providing oversight and ... of study Preferred three plus (5+) years of Security Management experience Experience with ...
Oversee multisite clinical trial research management operations including financial and contractual ... Serve as an operational resource for investigators, study teams, sponsors, and CROs. * Ensure ...
Oversee multisite clinical trial research management operations including financial and contractual ... Serve as an operational resource for investigators, study teams, sponsors, and CROs. * Ensure ...
... studies are conducted in compliance with regulatory requirements and corporate objectives. The ... Ensure vendor compliance with contractual obligations, timelines, and performance metrics for site ...
... studies are conducted in compliance with regulatory requirements and corporate objectives. The ... Ensure vendor compliance with contractual obligations, timelines, and performance metrics for site ...
Director, Security
Lexington, KY · On-site
... and contractual obligations. * Demonstrated ability to manage sensitive programs requiring ... Accredited four (4) year degree or global equivalent in applicable field of study and fourteen (14 ...
Director, Security
Lexington, KY · On-site
... and contractual obligations. * Demonstrated ability to manage sensitive programs requiring ... Accredited four (4) year degree or global equivalent in applicable field of study and fourteen (14 ...
... monotherapy and combination studies of its investigational first-in-class WEE1 inhibitor ... Manage and oversee activities and contractual relationship with Contract Manufacturing ...
... monotherapy and combination studies of its investigational first-in-class WEE1 inhibitor ... Manage and oversee activities and contractual relationship with Contract Manufacturing ...
Director Product Development
San Diego, CA · On-site
$200K - $250K/yr
... monotherapy and combination studies of its investigational first-in-class WEE1 inhibitor ... Manage and oversee activities and contractual relationship with Contract Manufacturing ...
Director Product Development
San Diego, CA · On-site
$200K - $250K/yr
... monotherapy and combination studies of its investigational first-in-class WEE1 inhibitor ... Manage and oversee activities and contractual relationship with Contract Manufacturing ...
Contractual Study Director information
See salary details
$59.1K is the 25th percentile. Wages below this are outliers.
$45K - $62K
30% of jobs
$62K - $79.1K
9% of jobs
The median wage is $92.2K / yr.
$79.1K - $96.1K
14% of jobs
$96.1K - $113.2K
0% of jobs
$113.2K - $130.2K
0% of jobs
$130.2K - $147.3K
1% of jobs
$147.3K - $164.3K
3% of jobs
$179.6K is the 75th percentile. Wages above this are outliers.
$164.3K - $181.4K
20% of jobs
$181.4K - $198.4K
6% of jobs
$198.4K - $215.5K
9% of jobs
$215.5K - $232.5K
7% of jobs
$45K
$128.4K
$232.5K
How much do contractual study director jobs pay per year?
Full-time
Medical, Dental, Vision, Life, Retirement
Posted 18 days ago
Job description
The Assistant Director of Research Programs will oversee the full lifecycle of complex, multi-disciplinary clinical studies within the LSU System, collaborating with elite academic, medical, and athletic partners. The AD will lead project planning, regulatory compliance, budgeting, inventory purchasing and maintenance, and team coordination to ensure that studies are executed with precision and scientific rigor. The ideal candidate has a strong background in managing multi-disciplinary clinical trials and thrives in innovative, cross-functional environments.
Job Responsibilities:
Cross-Functional Team Leadership: Lead and coordinate cross-functional project teams (clinical operations, data management, biostats, safety, regulatory, medical writing). Facilitate cross-functional team meetings, ensure documentation of decisions and action items. Act as Project Manager/Director to direct reports. Serve as the primary institute contact for internal and external stakeholders, and compile necessary data from ORED and IHPC research teams to provide regular project updates to stakeholders (40%).
Clinical Trial Planning & Execution: Lead planning, initiation, and execution of clinical trials from study start-up through closeout. Develop detailed project timelines, milestones, and resource allocation plans. Oversee site feasibility, selection, initiation, monitoring, and closeout. Work with clinical monitors, sponsors, and study teams to ensure high-quality site engagement and performance (25%).
Compliance, Risk, and Quality Oversight: Ensure compliance with ICH-GCP, FDA/EMA regulations, and internal SOPs. Proactively identify risks and develop/implement mitigation strategies, and lead issue resolution efforts to minimize study disruption and escalation. Support audit and inspection readiness activities (20%).
Resource Oversight: Development of clinical trial budgets for funding submissions and ensure adherence to project scope, budget, and deliverables. Oversee the selection, management, and performance of equipment and supply acquisition, maintenance, CROs and other vendors (e.g., labs, imaging providers, study specific vendors), equpment. Review and approve third party invoices and ensure adherence to contractual terms. Interface with the finance office in the Office of Research to ensure that allocation of resources to research projects are within the institute scope of funding (10%).
Other duties as assigned (5%).
Minimum Qualifications:
Bachelor's degree in a health-related field
3 years of experience in clinical research with some supervisory and clinical project management experience including but not limited to clinical trial budgeting, protocol and consent development, regulatory submissions, study implementation, and oversight of data collection and quality assurance. Strong knowledge of ICH-GCP, FDA/EMA regulatory requirements and clinical trial methodology, proficient in CTMS, EDC, eTMF, and Microsoft Project or equivalent tools.
Preferred Qualifications:
Master's degree in a health-related field
10 years of experience with a proven track record of managing complex, multi-site and/or multi-disciplinary studies preferred and some experience managing vendors, collaborators, sites, and cross-functional teams preferred.
LSU values skills, experience, and expertise. Candidates who have relevant experience in key job responsibilities are encouraged to apply -- a degree is not required as long as the candidate meets the required years of experience in the job description.
Additional Job Description:Special Instructions:Please provide a cover letter, resume, and three (3) professional references including name, title, phone number, and e-mail address.Please attach ALL required documents under the "Resume/CV" section of your application.
A copy of your transcript(s) may be attached to your application (if available). However, original transcripts are required before hiring.
Due to the nature of the position and/or position responsibilities, this position shall be subject to pre-employment screenings in accordance with University Policy as required and RS:17 screenings (https://www.legis.la.gov/legis/Law.aspx?p=y&d=1297548).
For questions or concerns about updating your application with attachments (e.g., resumes, RS:17 documents), date of birth, or reactivating applications, please contact the LSU Human Resources Management Office at 225-578-8200 or email HR@lsu.edu.
For questions or concerns regarding the status of your application or salary ranges, please contact Neil Johannsen at njohan1@lsu.edu.
Skills Needed:
Preferred Skills:
Posting Date:June 26, 2026Closing Date (Open Until Filled if No Date Specified):October 14, 2026Additional Position Information:Background Check - An offer of employment is contingent on a satisfactory pre-employment background check.
Benefits - LSU offers outstanding benefits to eligible employees and their dependents including health, life, dental, and vision insurance; flexible spending accounts; retirement options; various leave options; paid holidays; wellness benefits; tuition exemption for qualified positions; training and development opportunities; employee discounts; and more!
Positions approved to work outside the State of Louisiana shall be employed through Louisiana State University's partner, nextSource Workforce Solutions, for Employer of Record Services including but not limited to employment, benefits, payroll, and tax compliance. Positions employed through Employer of Record Services will be offered benefits and retirement as applicable through their provider and will not be eligible for State of Louisiana benefits and retirement.
Essential Position (Y/N):LSU is an Equal Opportunity Employer.All candidates must have valid U.S. work authorization at the time of hire and maintain that valid work authorization throughout employment. Changes in laws, regulations, or government policies may impact the university's ability to employ individuals in certain positions.
HCM Contact Information:For questions or concerns related to updating your application with attachments (e.g., resumes, RS:17 documents), date of birth, or reactivating applications, please contact the LSU Human Resources Management Office at 225-578-8200 or email HR@lsu.edu. For questions or concerns regarding the status of your application or salary ranges, please contact the department using the information provided in the Special Instructions section of this job posting.