We are hiring a Manager of Site Operations!
Are you a leader with excellent organizational skills, capable of adapting to unexpected changes? Do you have the ability to oversee both the big picture and day-to-day tasks? If so, keep reading!
This role is perfect for someone who can inspire cross-functional teams to collaborate for the best quality outcomes and positive relationships.
Responsibilities:
- Oversee and support functions within Site Operations.
- Supervise Site Operations team members, including CRAs, CTMs, and RAs.
- Set clear job expectations, assess training needs, and provide necessary training.
- Assist team members in developing improvement and innovation goals with periodic reviews.
- Manage multidisciplinary project team activities, propose resolutions to issues, and provide routine updates to the Director of Operations.
- Ensure appropriate resourcing and personnel allocation for evolving business needs.
- Provide strategic input, oversee deliverables, and ensure compliance with policies and regulations.
- Collaborate with the Director of Operations on evaluating metrics and implementing necessary changes.
- Develop and review/approve applicable Site Operations SOPs and WIs.
- Assist Business Development with benchmarking for budgets and development of Sponsor proposals.
- Provide mentoring, support, and backup for relevant Site Operations project activities.
Requirements:
- BA/BS in a scientific field or equivalent experience.
- Minimum of 5 years of experience in clinical trials.
- Thorough knowledge of Good Clinical Practice guidelines and applicable FDA and ICH regulations.
- Experience with MS Office tools, including Project PowerPoint, SharePoint, Word, and Excel.
- Excellent interpersonal communication and organizational skills.
- Ability to manage conflicts and resolve problems effectively.
- Willingness to travel up to 15%.
Note: Viable applicants will be required to pass a background and education verification check.
Targeted Compensation:
$110,000 – $115,000 annually
About CPC:
CPC is an academic research organization offering full-service clinical trial design, oversight, and management. With over 30 years of experience, CPC has provided services to over 150 clinical trials in various therapeutic areas.
CPC offers:
- Comprehensive benefits package
- Matching 401(k) plan
- 10 paid holidays
- 15 – 25 vacation days based on years of service
- Paid sick time
- In-suite exercise and relaxation room
- Monthly fun events
- Flexible and remote work schedules
An Equal Opportunity Employer
CPC provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, national origin, sex, gender identity, veteran status, marital status, sexual orientation, age forty and over, disability, genetic information, or any other status protected by applicable federal, state, or local law.
Applicants with disabilities may be entitled to reasonable accommodation under the Americans with Disabilities Act (ADA) and certain state or local laws. If you need assistance, please email our Human Resources team at [email protected].
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