Clinical Operations Associate Director - San Diego, CA | Biospace
Get Our FREE Industry eNewsletter

Clinical Operations Associate Director

Receptos

Apply
Location:
San Diego, CA
Posted Date:
2/6/2017
Position Type:
Full time
Job Code:
2017ADClinOps02
Salary:
Required Education:
Bachelors Degree
Areas of Expertise Desired:
Clinical Operations,

Job Description

Receptos, a wholly-owned subsidiary of Celgene, is a San Diego-based biopharmaceutical company focused on discovering, developing and commercializing innovative therapeutics in immune disease. We are currently searching for an Associate Director, Clinical Operations.

The primary role of the Associate Director, Clinical Operations, is to coordinate, manage and supervise operational activities associated with clinical development programs, including:  maintenance of essential study documentation, dissemination of key information to clinical advisors, CROs and ancillary vendor partners and participating investigators; establishing and managing contracts and budgets with clinical investigators and clinical trial service providers; preparing clinical trial documents (e.g., protocols, investigators brochures, site operations manuals) and;  ensuring that these activities are conducted in accordance with all applicable regulations, and ICH and GCP guidance standards.  In addition, this individual may prepare departmental standard operating procedures, working procedures and templates. This role is also responsible for tracking and reporting budgets and timelines for clinical programs.

This position requires a proven track record of increasing responsibility in clinical operations, and successful management of clinical research and support personnel, departmental budgets and timelines in the pharmaceutical/biotech industry.

Experience with large, complex late stage global clinical development programs required. NDA filing and therapeutic experience in a related field highly desired.

Major Responsibilities:

•   Evaluate potential contract research organizations (CROs), vendors and other service providers for use in Receptos clinical studies.
•   Ensure qualification of CROs, vendors and service providers in accordance with Receptos SOPs.
•   Supervises Clinical Trial Managers (CTMs) and/or Clinical Research Associates (CRAs).
•   Manage vendors providing the operational functions of Receptos clinical programs.  Participate in functional guidance, training, education and evaluation of vendors personnel.
•   Supervise the activities of CROs, contractors and other vendors as they are related to the clinical programs.
•   Ensure screening and evaluation of potential Investigators to ensure compliance with regulatory and corporate requirements.
•   Supervise negotiation of Investigator agreements and grants appropriate to the clinical programs.
•   Ensure review and approval of written reports of all site monitoring visits prepared by CRAs to ensure they are completed in a timely fashion and according to Federal regulations, GCP and SOPs.
•   Ensure maintenance of essential documents associated with Receptos clinical trials, in accordance with applicable regulations and international guidance’s.
•   Participate in corporate committees, task forces, technical or business meetings as requested.
•   Ensure timely and appropriate response to clinical investigator site issues or other study management problems.  Ensure maintenance of documentation in appropriate reports of all communications, particularly those in which patient or protocol issues are discussed.
•   Prepare communication and status reports to provide updates/information to senior management.
•   Direct clinical operations activities in preparation of interim analyses, clinical study reports, annual reports and other clinical documents.
•   Demonstrate mastery of FDA and ICH rules, regulations and guidelines governing conduct of clinical studies, clinical protocols, investigator brochures and other materials.
•   Develop and maintain departmental standard operating procedures (SOPs) in collaboration with Clinical Development, Regulatory Affairs and Quality Assurance.
•   Represent Receptos in a professional manner; establish and maintain good relationships with Investigators, advisors, other study personnel, clients and vendors.
•   Attend seminars, Investigator meetings, project team meetings, educational conferences/training sessions, etc.
•   Other duties as assigned.

Requirements

•   Bachelor’s Degree or Graduate Degree in a field of science or nursing, preferably biology, chemistry, pharmacy, or other field related to human study.  
•   Knowledge of medical terminology required.  
•   Computer literacy (Word/Excel), familiarity with clinical database concepts, and experience with statistical principles is required.  
•   Position may require travel expected to be no more than 20% (domestic and international).

If qualified and interested, please visit https://receptos.hyrell.com/UI/Views/Applicant/VirtualStepCareers.aspx to view the complete job description and the application process.

Receptos, a wholly-owned subsidiary of Celgene, offers a dynamic work environment, an attractive salary (commensurate with experience) and an annual incentive program.  As well, Receptos offers a comprehensive benefits package which includes Equity, 401(k), Vacation, Holidays and company-subsidized insurance coverage (Medical, Dental, Vision, Flexible Spending Accounts, Life, AD&D, Short-Term Disability and Long-Term Disability).  Receptos is an Equal Opportunity Employer.