Senior Project Director
Growing CRO in Northern Colorado seeks highly motivated DVM to serve as Senior Project Director. Candidate should have knowledge and expertise in pharmaceutical compound toxicology / medical devices / pre-clinical safety assessment. Experience working in a GLP/GCP compliant environment as well as familiarity with US and international regulatory guidelines is desirable. The successful individual will possess excellent verbal and written skills and excellent scientific expertise to deal with customers. He/She will serve as protocol developer and study director on surgical and toxicology studies and assist in designing studies and overseeing their technical conduct. The individual will perform project management functions including estimating, planning, scheduling, monitoring, evaluating, documenting, and reporting to ensure successful completion of multiple projects. Previous pre-clinical or clinical CRO experience is highly desirable.
The candidate will be focused on implementation of client studies from protocol development through final reporting.
Responsibilities include:
- Provide technical leadership and guidance in surgical, anesthesia and other surgical suite techniques,
- Produce study protocols and reports to meet client and regulatory requirements,
- Ensure that studies are performed in accordance with the study protocol, company standards, and required scientific and regulatory standards,
- Ensure all study communication is documented and maintained to meet client, company, and regulatory requirements,
- Project management including the ability to handle multiple priorities and to utilize resources effectively,
- Work with technical staff to develop new techniques as appropriate,
- Demonstrate exemplary customer relations skills,
- Perform development, coaching and management of junior study directors,
- Demonstrate the ability to inspire effective teamwork, motivate staff and encourage by example.
Qualifications include:
- DVM required, Board certification is desirable,
- PhD/MS or other advanced degree in toxicology, anatomy, or related field,
- At least 5 years of experience in a research, clinical or pre-clinical environment,
- Project management experience, preferably in a pharmaceutical, device or CRO environment,
- Demonstrated expertise in surgical and anesthesia techniques,
- Familiarity with GLP/GCP protocol development and implementation,
- Familiarity with endoscopic/laparoscopic techniques is desirable,
- Familiarity with the use of a C-ARM will be a plus,
- Must be personable, flexible and a team player who can negotiate and liaise with clients and staff in a professional manner.
Compensation:
Salary will be commensurate with qualifications and experience.
Send resumes to hiring@careresearchllc.com.